首页 > 最新文献

Journal of energy storage最新文献

英文 中文
A self-actuating internal stirring mechanism to maintain dispersion uniformity in paraffin/carbon nanotube phase change composites 一种保持石蜡/碳纳米管相变复合材料分散均匀性的自驱动内搅拌机制
IF 8.9 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-04-01 Epub Date: 2026-02-03 DOI: 10.1016/j.est.2026.120891
Yinfeng Xia , Takushi Saito
Paraffin-based Phase Change Materials (PCMs) are promising candidates for Thermal Energy Storage (TES) systems, but their low thermal conductivity is often a significant drawback. While the addition of high-conductivity nanoparticles like Carbon Nanotubes (CNTs) can address this, long-term performance can be compromised as CNTs agglomerate and separate from the paraffin matrix over repeated thermal cycles. This degradation is driven by fundamental solidification phenomena such as particle pushing, which leads to a breakdown of the conductive nanoparticle network. To address this, we developed a novel self-actuating internal stirring mechanism that maintains dispersion uniformity without external power. Leveraging the volumetric expansion of the PCM itself (the “wax motor” principle), the device autonomously converts thermal energy into rotational mixing during the melting phase. A Computational Fluid Dynamics (CFD)-optimized Sawtooth impeller was engineered to generate high local shear rates (>140 s−1) sufficient to initiate CNT deagglomeration. Experimental validation over 50 thermal cycles demonstrated that the active stirring effectively suppressed phase separation. From the 128.7% initial improvement over pure paraffin, the stirred composite retained ∼90% of its initial thermal conductivity (0.391 W/(m·K)), significantly outperforming the unstirred control which degraded by 26% (0.334 W/(m·K)). This work establishes a successful proof-of-concept for a semi-active stabilization strategy to overcome the long-term reliability barriers in latent heat storage systems.
石蜡基相变材料(PCMs)是热能存储(TES)系统的有前途的候选者,但其低导热性往往是一个重大的缺点。虽然添加高导电性纳米颗粒(如碳纳米管)可以解决这个问题,但长期性能可能会受到影响,因为碳纳米管会在重复的热循环中与石蜡基体团聚和分离。这种退化是由基本的凝固现象驱动的,比如粒子推动,这会导致导电纳米粒子网络的破坏。为了解决这个问题,我们开发了一种新的自驱动内部搅拌机构,无需外部动力即可保持分散均匀性。利用PCM本身的体积膨胀(“蜡马达”原理),该装置在熔化阶段自动将热能转化为旋转混合。计算流体动力学(CFD)优化的锯齿形叶轮能够产生高的局部剪切速率(>140 s−1),足以启动碳纳米管脱团聚。50多个热循环的实验验证表明,主动搅拌有效地抑制了相分离。与纯石蜡相比,经过搅拌的复合材料的初始导热系数提高了128.7%,保持了约90%的初始导热系数(0.391 W/(m·K)),显著优于未搅拌的对照组,后者的导热系数下降了26% (0.334 W/(m·K))。这项工作为半主动稳定策略建立了一个成功的概念验证,以克服潜热储存系统的长期可靠性障碍。
{"title":"A self-actuating internal stirring mechanism to maintain dispersion uniformity in paraffin/carbon nanotube phase change composites","authors":"Yinfeng Xia ,&nbsp;Takushi Saito","doi":"10.1016/j.est.2026.120891","DOIUrl":"10.1016/j.est.2026.120891","url":null,"abstract":"<div><div>Paraffin-based Phase Change Materials (PCMs) are promising candidates for Thermal Energy Storage (TES) systems, but their low thermal conductivity is often a significant drawback. While the addition of high-conductivity nanoparticles like Carbon Nanotubes (CNTs) can address this, long-term performance can be compromised as CNTs agglomerate and separate from the paraffin matrix over repeated thermal cycles. This degradation is driven by fundamental solidification phenomena such as particle pushing, which leads to a breakdown of the conductive nanoparticle network. To address this, we developed a novel self-actuating internal stirring mechanism that maintains dispersion uniformity without external power. Leveraging the volumetric expansion of the PCM itself (the “wax motor” principle), the device autonomously converts thermal energy into rotational mixing during the melting phase. A Computational Fluid Dynamics (CFD)-optimized Sawtooth impeller was engineered to generate high local shear rates (&gt;140 s<sup>−1</sup>) sufficient to initiate CNT deagglomeration. Experimental validation over 50 thermal cycles demonstrated that the active stirring effectively suppressed phase separation. From the 128.7% initial improvement over pure paraffin, the stirred composite retained ∼90% of its initial thermal conductivity (0.391 W/(m·K)), significantly outperforming the unstirred control which degraded by 26% (0.334 W/(m·K)). This work establishes a successful proof-of-concept for a semi-active stabilization strategy to overcome the long-term reliability barriers in latent heat storage systems.</div></div>","PeriodicalId":15942,"journal":{"name":"Journal of energy storage","volume":"153 ","pages":"Article 120891"},"PeriodicalIF":8.9,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146098540","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Research advances in modifying high-performance lithium‑sulfur battery separator with bimetallic metal-organic frameworks 双金属金属有机骨架改性高性能锂硫电池隔膜的研究进展
IF 8.9 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-04-01 Epub Date: 2026-02-04 DOI: 10.1016/j.est.2026.120957
Yu Li , Yao Wu , Bofang Shi , Muhammad Jamshed , Ye Zhang , Taohong He , Yunhui Chen , Cheng Zhang , Honghui Yang
Lithium‑sulfur batteries (LSBs) are promising candidates for next-generation energy storage systems due to their high theoretical specific capacity (1675 mAh g−1). However, practical applications are hindered by the polysulfide (LiPS) shuttle effect and lithium dendrite growth. Metal-organic frameworks (MOFs), with high porosity, tunable pore size, and abundant active sites, are ideal materials for separator modification to suppress LiPS migration. Compared to monometallic MOFs, bimetallic MOFs exhibit superior electrocatalytic activity and ion transport due to synergistic effects. This paper summarizes recent progress in the use of bimetallic metal-organic frameworks for separator modification, emphasizing design strategies, performance optimization, and electrochemical differences with monometallic MOFs based on experimental data. It also analyzes the current limitations of LSB research. To advance commercialization, strategies such as designing multifunctional integrated separators for improved interfacial stability and LiPS confinement, screening bimetallic catalysts to enhance redox kinetics, and optimizing scalable manufacturing processes were proposed. These targeted approaches aim to overcome bottlenecks and accelerate the transition of LSB technology from lab-scale research to real-world applications.
锂硫电池(lsb)由于其高理论比容量(1675 mAh g−1)而成为下一代储能系统的有希望的候选者。然而,实际应用受到多硫化物(LiPS)穿梭效应和锂枝晶生长的阻碍。金属有机骨架(mof)具有高孔隙率、孔径可调、活性位点丰富等特点,是抑制LiPS迁移的理想材料。与单金属mof相比,双金属mof由于协同效应表现出更强的电催化活性和离子传输能力。本文综述了近年来利用双金属金属有机骨架对隔膜进行改性的研究进展,重点介绍了基于实验数据的设计策略、性能优化以及与单金属mof的电化学差异。分析了当前LSB研究的局限性。为了推进商业化,研究人员提出了诸如设计多功能集成分离器以提高界面稳定性和LiPS约束、筛选双金属催化剂以提高氧化还原动力学以及优化可扩展制造工艺等策略。这些有针对性的方法旨在克服瓶颈,加速LSB技术从实验室规模的研究向现实世界应用的过渡。
{"title":"Research advances in modifying high-performance lithium‑sulfur battery separator with bimetallic metal-organic frameworks","authors":"Yu Li ,&nbsp;Yao Wu ,&nbsp;Bofang Shi ,&nbsp;Muhammad Jamshed ,&nbsp;Ye Zhang ,&nbsp;Taohong He ,&nbsp;Yunhui Chen ,&nbsp;Cheng Zhang ,&nbsp;Honghui Yang","doi":"10.1016/j.est.2026.120957","DOIUrl":"10.1016/j.est.2026.120957","url":null,"abstract":"<div><div>Lithium‑sulfur batteries (LSBs) are promising candidates for next-generation energy storage systems due to their high theoretical specific capacity (1675 mAh g<sup>−1</sup>). However, practical applications are hindered by the polysulfide (LiPS) shuttle effect and lithium dendrite growth. Metal-organic frameworks (MOFs), with high porosity, tunable pore size, and abundant active sites, are ideal materials for separator modification to suppress LiPS migration. Compared to monometallic MOFs, bimetallic MOFs exhibit superior electrocatalytic activity and ion transport due to synergistic effects. This paper summarizes recent progress in the use of bimetallic metal-organic frameworks for separator modification, emphasizing design strategies, performance optimization, and electrochemical differences with monometallic MOFs based on experimental data. It also analyzes the current limitations of LSB research. To advance commercialization, strategies such as designing multifunctional integrated separators for improved interfacial stability and LiPS confinement, screening bimetallic catalysts to enhance redox kinetics, and optimizing scalable manufacturing processes were proposed. These targeted approaches aim to overcome bottlenecks and accelerate the transition of LSB technology from lab-scale research to real-world applications.</div></div>","PeriodicalId":15942,"journal":{"name":"Journal of energy storage","volume":"153 ","pages":"Article 120957"},"PeriodicalIF":8.9,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146191794","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fault-engineered lithiophilic layer on current collectors for high-performance anode-free lithium metal batteries 高性能无阳极锂金属电池集流器上的缺陷工程亲锂层
IF 8.9 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-04-01 Epub Date: 2026-02-12 DOI: 10.1016/j.est.2026.121053
Jianfei Lei , Chenming Liang , Zexin Liang , Haoyu Lou , Xiaofeng Duan , Mengting Zhang , Xiujuan Jin , Shaobo Huang , Zhaowu Wang
Anode-free lithium metal batteries (AFLMBs) have attracted significant attention due to their high energy density, low cost, and enhanced safety. However, the practical application is hindered by a relatively short cycle life and rapid capacity fading, primarily attributed to the continuous loss of active lithium. Although numerous efforts have been devoted to modifying the surface of current collectors to effectively regulate lithium deposition behavior, a critical issue remains underexplored: irreversible lithium deposition can occur on the metallic casing of the battery. This phenomenon may lead to significant loss of cyclable lithium and substantially degrade Coulombic efficiency, thereby compromising the long-term cycle stability. Here, we engineered a lithiophilic layer with tailored fault layer on the current collector to suppress the irreversible lithium deposition on the metallic casing. A lithiophobic copper interlayer was strategically integrated between the metallic casing and a lithiophilic MXene layer to form a fault-lithiophilic architecture. This hierarchical design facilitates the directional migration of lithium ions, effectively suppressing their irreversible deposition on the metallic casing surface, thereby significantly enhancing the overall performance of the AFLMBs. Compared to the copper current collector, the engineered collector reduces the lithium nucleation overpotential by 37.8% and achieves over 350 stable cycles at a current density of 1 mA cm−2 with 1 mAh cm−2 capacity. When paired with a commercial LiFePO4 cathode, the engineered anode demonstrates excellent cycling stability and rate capability, and no significant capacity degradation was detected after 400 cycles at a current density of 1C.
无阳极锂金属电池(aflmb)因其能量密度高、成本低、安全性强等优点而备受关注。然而,由于活性锂的不断损耗,其循环寿命相对较短,容量衰减快,阻碍了其实际应用。尽管人们已经做出了大量的努力来修改集流器的表面,以有效地调节锂的沉积行为,但一个关键的问题仍未得到充分的探讨:电池的金属外壳上可能发生不可逆的锂沉积。这种现象可能导致可循环锂的大量损失,库仑效率大幅降低,从而影响长期循环稳定性。在这里,我们设计了一个具有定制故障层的亲锂层,以抑制金属外壳上不可逆的锂沉积。在金属套管和亲石的MXene层之间战略性地整合了一层疏石铜夹层,形成了一个断层-亲石结构。这种分层设计促进了锂离子的定向迁移,有效抑制了锂离子在金属套管表面的不可逆沉积,从而显著提高了aflmb的整体性能。与铜集热器相比,该集热器降低了37.8%的锂成核过电位,并在1ma cm - 2的电流密度和1mah cm - 2的容量下实现了超过350次的稳定循环。当与商用LiFePO4阴极配对时,工程阳极表现出出色的循环稳定性和速率能力,并且在1C电流密度下循环400次后没有检测到明显的容量下降。
{"title":"Fault-engineered lithiophilic layer on current collectors for high-performance anode-free lithium metal batteries","authors":"Jianfei Lei ,&nbsp;Chenming Liang ,&nbsp;Zexin Liang ,&nbsp;Haoyu Lou ,&nbsp;Xiaofeng Duan ,&nbsp;Mengting Zhang ,&nbsp;Xiujuan Jin ,&nbsp;Shaobo Huang ,&nbsp;Zhaowu Wang","doi":"10.1016/j.est.2026.121053","DOIUrl":"10.1016/j.est.2026.121053","url":null,"abstract":"<div><div>Anode-free lithium metal batteries (AFLMBs) have attracted significant attention due to their high energy density, low cost, and enhanced safety. However, the practical application is hindered by a relatively short cycle life and rapid capacity fading, primarily attributed to the continuous loss of active lithium. Although numerous efforts have been devoted to modifying the surface of current collectors to effectively regulate lithium deposition behavior, a critical issue remains underexplored: irreversible lithium deposition can occur on the metallic casing of the battery. This phenomenon may lead to significant loss of cyclable lithium and substantially degrade Coulombic efficiency, thereby compromising the long-term cycle stability. Here, we engineered a lithiophilic layer with tailored fault layer on the current collector to suppress the irreversible lithium deposition on the metallic casing. A lithiophobic copper interlayer was strategically integrated between the metallic casing and a lithiophilic MXene layer to form a fault-lithiophilic architecture. This hierarchical design facilitates the directional migration of lithium ions, effectively suppressing their irreversible deposition on the metallic casing surface, thereby significantly enhancing the overall performance of the AFLMBs. Compared to the copper current collector, the engineered collector reduces the lithium nucleation overpotential by 37.8% and achieves over 350 stable cycles at a current density of 1 mA cm<sup>−2</sup> with 1 mAh cm<sup>−2</sup> capacity. When paired with a commercial LiFePO<sub>4</sub> cathode, the engineered anode demonstrates excellent cycling stability and rate capability, and no significant capacity degradation was detected after 400 cycles at a current density of 1C.</div></div>","PeriodicalId":15942,"journal":{"name":"Journal of energy storage","volume":"153 ","pages":"Article 121053"},"PeriodicalIF":8.9,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146171802","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Lithium-doped high-entropy oxides for advanced lithium-ion storage: enhanced electrochemical performance and tunable magnetism 用于先进锂离子存储的掺锂高熵氧化物:增强的电化学性能和可调磁性
IF 8.9 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-04-01 Epub Date: 2026-02-12 DOI: 10.1016/j.est.2026.120934
Shengxi Zhao , Kaiyu Xie , Asma Rezaei , Ali Reza Kamali
High-entropy oxides (HEOs) are emerging as next-generation anode materials for lithium-ion batteries (LIBs) owing to their structural stability and high theoretical capacity. Here, we present a simple and green strategy to enhance their electrochemical performance via lithium doping. Single-phase (FeCoNiCrMn)3O4 HEO is synthesized through a solid-state reaction and subsequently Li-doped using a one-pot molten salt method. Li incorporation (3.85 at.%) reduces the lattice constant by 1.34%, increases the particle size from 60-80 nm to 80-140 nm and boosts surface oxygen vacancies from 18.8% to 26.7%, as revealed by electron paramagnetic resonance. Li-doped HEO (Li-HEO) delivers a high reversible capacity of 741.9 mAh g−1 after 250 cycles at 100 mA g−1 with superior rate capability, lower charge-transfer resistance (31.6 Ω) and a Li-ion diffusion coefficient up to 10–10.3 cm2 s−1, significantly outperforming the pristine HEO (135.9 Ω; 10–12.1 cm2 s−1). In-situ XRD confirms the retention of the spinel structure during cycling, indicating excellent structural stability. A full cell pairing Li-HEO with LiFePO4 achieves 368.2 mAh g−1 and 266.1 Wh kg−1 after 100 cycles, surpassing the HEO-based counterpart by 17.6%. Magnetic measurements reveal an unprecedentedly high saturation magnetization in pristine HEO (34.0 emu g−1), exceeding that of alternative HEOs reported in the literature. Upon Li doping, the saturation magnetization decreases to 15.0 emu g−1, accompanied by enhanced soft-magnetic behavior as evidenced by the reduction in coercivity from 261.2 to 91.1 Oe. This tunable combination of electrochemical performance and magnetic properties supports both efficient energy storage and facile electrode recycling. Overall, this work demonstrates a scalable and eco-friendly lithium doping approach to unlock the high-rate and long-cycle potential of HEO anodes for advanced LIBs.
高熵氧化物(HEOs)因其结构稳定、理论容量高而成为锂离子电池(LIBs)的下一代负极材料。在这里,我们提出了一种简单的绿色策略,通过锂掺杂来提高它们的电化学性能。通过固相反应合成了单相(FeCoNiCrMn)3O4 HEO,随后采用一锅熔盐法掺锂。Li掺入(3.85 at)。电子顺磁共振结果显示,纳米二氧化钛的晶格常数降低了1.34%,颗粒尺寸从60 ~ 80 nm增加到80 ~ 140 nm,表面氧空位从18.8%提高到26.7%。锂掺杂HEO (Li-HEO)在100 mA g - 1下循环250次后具有741.9 mAh g - 1的高可逆容量,具有优越的倍率能力,更低的电荷转移电阻(31.6 Ω)和锂离子扩散系数高达10-10.3 cm2 s - 1,显著优于原始HEO (135.9 Ω; 10-12.1 cm2 s - 1)。原位XRD证实了循环过程中尖晶石结构的保留,表明其具有良好的结构稳定性。锂- heo与LiFePO4的全电池在100次循环后可达到368.2 mAh g−1和266.1 Wh kg−1,比基于heo的锂- heo电池高出17.6%。磁测量显示,原始HEO具有前所未有的高饱和磁化强度(34.0 emu g−1),超过了文献中报道的其他HEO。Li掺杂后,饱和磁化强度降低到15.0 emu g−1,矫顽力从261.2降低到91.1 Oe,软磁行为增强。这种电化学性能和磁性的可调组合支持高效的能量存储和易于电极回收。总的来说,这项工作展示了一种可扩展的、环保的锂掺杂方法,可以解锁用于先进锂离子电池的HEO阳极的高速率和长周期潜力。
{"title":"Lithium-doped high-entropy oxides for advanced lithium-ion storage: enhanced electrochemical performance and tunable magnetism","authors":"Shengxi Zhao ,&nbsp;Kaiyu Xie ,&nbsp;Asma Rezaei ,&nbsp;Ali Reza Kamali","doi":"10.1016/j.est.2026.120934","DOIUrl":"10.1016/j.est.2026.120934","url":null,"abstract":"<div><div>High-entropy oxides (HEOs) are emerging as next-generation anode materials for lithium-ion batteries (LIBs) owing to their structural stability and high theoretical capacity. Here, we present a simple and green strategy to enhance their electrochemical performance via lithium doping. Single-phase (FeCoNiCrMn)<sub>3</sub>O<sub>4</sub> HEO is synthesized through a solid-state reaction and subsequently Li-doped using a one-pot molten salt method. Li incorporation (3.85 at.%) reduces the lattice constant by 1.34%, increases the particle size from 60-80 nm to 80-140 nm and boosts surface oxygen vacancies from 18.8% to 26.7%, as revealed by electron paramagnetic resonance. Li-doped HEO (Li-HEO) delivers a high reversible capacity of 741.9 mAh g<sup>−1</sup> after 250 cycles at 100 mA g<sup>−1</sup> with superior rate capability, lower charge-transfer resistance (31.6 Ω) and a Li-ion diffusion coefficient up to 10<sup>–10.3</sup> cm<sup>2</sup> s<sup>−1</sup>, significantly outperforming the pristine HEO (135.9 Ω; 10<sup>–12.1</sup> cm<sup>2</sup> s<sup>−1</sup>). In-situ XRD confirms the retention of the spinel structure during cycling, indicating excellent structural stability. A full cell pairing Li-HEO with LiFePO<sub>4</sub> achieves 368.2 mAh g<sup>−1</sup> and 266.1 Wh kg<sup>−1</sup> after 100 cycles, surpassing the HEO-based counterpart by 17.6%. Magnetic measurements reveal an unprecedentedly high saturation magnetization in pristine HEO (34.0 emu g<sup>−1</sup>), exceeding that of alternative HEOs reported in the literature. Upon Li doping, the saturation magnetization decreases to 15.0 emu g<sup>−1</sup>, accompanied by enhanced soft-magnetic behavior as evidenced by the reduction in coercivity from 261.2 to 91.1 Oe. This tunable combination of electrochemical performance and magnetic properties supports both efficient energy storage and facile electrode recycling. Overall, this work demonstrates a scalable and eco-friendly lithium doping approach to unlock the high-rate and long-cycle potential of HEO anodes for advanced LIBs.</div></div>","PeriodicalId":15942,"journal":{"name":"Journal of energy storage","volume":"153 ","pages":"Article 120934"},"PeriodicalIF":8.9,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146171803","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Immersion cooling control for ununiform degraded lithium-ion batteries under fast charging 快充条件下不均匀退化锂离子电池的浸没冷却控制
IF 8.9 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-04-01 Epub Date: 2026-02-02 DOI: 10.1016/j.est.2026.120820
Liqin Qian , Wei Xiao , Gensheng Fei , Chengyu Xia , Yahui Yi , Tiancai Ma , Siqi Chen
Overheating hazard of nonuniformly degraded battery systems limits battery All-lifespan safe applications. However, the evolution principle and corresponding strategies are still unlocked. Therefore, this study proposes a dynamic immersion cooling strategy to address the All-lifespan 4C fast charging issue of nonuniformly degraded modules. Firstly, heat generation of degraded batteries are experimentally measured to be more significant due to severe side reactions under fast charging, inducing nonuniform heat accumulation-degradation in systems. Moreover, maximum temperature (Tmax: 437.5 K) and temperature standard deviation (TSD: 5.5 K) are detected in the harshest nonuniformly degraded module after 4C fast charging for 15 min, which can be controlled within an acceptable level (Tmax: 316.85 K, TSD: 2.3 K) under the coolant flow rate threshold 0.005 kg/s with the cooling scheme. Furthermore, dynamic coolant flow rate threshold is investigated for different nonuniformly degraded modules, cooling strategies are evaluated form the temperature control (decrement and uniformity) and energy cost, coolant threshold q1 is selected with higher thermal and economically efficiency. This study provides guidance for All-lifespan thermal management in the next-generation energy storage devices, considering the nonuniformly degradation effect.
非均匀退化电池系统的过热危险限制了电池的全寿命安全应用。然而,进化原理和相应的策略仍未被解开。因此,本研究提出了一种动态浸没冷却策略,以解决非均匀退化模块的全寿命4C快速充电问题。首先,通过实验测量,在快速充电条件下,由于严重的副反应,降解电池产生的热量更加显著,从而导致系统中不均匀的热量积累-降解。此外,在4℃快速充电15 min后,最恶劣非均匀退化模块的最高温度(Tmax: 437.5 K)和温度标准偏差(TSD: 5.5 K)可以在冷却剂流量阈值0.005 kg/s下控制在可接受的水平(Tmax: 316.85 K, TSD: 2.3 K)。此外,研究了不同非均匀降解模块的动态冷却剂流量阈值,从温度控制(减量和均匀性)和能量成本方面对冷却策略进行了评估,选择了热效率和经济效率较高的冷却剂阈值q1。该研究为考虑非均匀退化效应的下一代储能器件的全寿命热管理提供了指导。
{"title":"Immersion cooling control for ununiform degraded lithium-ion batteries under fast charging","authors":"Liqin Qian ,&nbsp;Wei Xiao ,&nbsp;Gensheng Fei ,&nbsp;Chengyu Xia ,&nbsp;Yahui Yi ,&nbsp;Tiancai Ma ,&nbsp;Siqi Chen","doi":"10.1016/j.est.2026.120820","DOIUrl":"10.1016/j.est.2026.120820","url":null,"abstract":"<div><div>Overheating hazard of nonuniformly degraded battery systems limits battery All-lifespan safe applications. However, the evolution principle and corresponding strategies are still unlocked. Therefore, this study proposes a dynamic immersion cooling strategy to address the All-lifespan 4C fast charging issue of nonuniformly degraded modules. Firstly, heat generation of degraded batteries are experimentally measured to be more significant due to severe side reactions under fast charging, inducing nonuniform heat accumulation-degradation in systems. Moreover, maximum temperature (<em>T</em><sub><em>max</em></sub>: 437.5 K) and temperature standard deviation (<em>TSD</em>: 5.5 K) are detected in the harshest nonuniformly degraded module after 4C fast charging for 15 min, which can be controlled within an acceptable level (<em>T</em><sub><em>max</em></sub>: 316.85 K, <em>TSD</em>: 2.3 K) under the coolant flow rate threshold 0.005 kg/s with the cooling scheme. Furthermore, dynamic coolant flow rate threshold is investigated for different nonuniformly degraded modules, cooling strategies are evaluated form the temperature control (decrement and uniformity) and energy cost, coolant threshold <em>q1</em> is selected with higher thermal and economically efficiency. This study provides guidance for All-lifespan thermal management in the next-generation energy storage devices, considering the nonuniformly degradation effect.</div></div>","PeriodicalId":15942,"journal":{"name":"Journal of energy storage","volume":"153 ","pages":"Article 120820"},"PeriodicalIF":8.9,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146098480","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The C6N2 monolayer as a universal anode for lithium/sodium/potassium-ion batteries: A first-principles study C6N2单层作为锂/钠/钾离子电池的通用阳极:第一性原理研究
IF 8.9 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-04-01 Epub Date: 2026-02-03 DOI: 10.1016/j.est.2026.120902
Ruotong Gao , Haoxiang Zhang , Hai Wu , XingKao Zhang , Hanqing Li , Xiangjie Fu , Hongying Hou , Ju Rong , Xiaohua Yu
Two-dimensional(2D) carbon‑nitrogen materials have emerged as promising candidates for anode materials in metal-ion batteries (MIBs) due to their exceptional electrical conductivity and structural stability. This paper employs first-principles calculations to systematically investigate the performance of C6N2 in Li+/Na+/K+ batteries. Results indicate that the monolayer C6N2 has an optimal electronic structure with excellent conductivity. Li+, Na+, and K+ also exhibit high adsorption energies, providing stable adsorption sites that enhance cycling stability. Analysis of C6N2's ionic diffusion properties revealed a low diffusion energy barrier, supporting efficient performance during rapid charge-discharge cycles. Further theoretical calculations indicate that C6N2 exhibits theoretical specific capacities for Li+/Na+/K+ as high as 1596 mAh/g, 1197 mAh/g, and 997 mAh/g respectively, significantly surpassing many conventional anode materials. Furthermore, it exhibits minimal open-circuit voltage (OCV) variation, meeting the requirements for stable battery operation. Overall, the outstanding electrochemical performance and structural characteristics of C6N2 confer broad application prospects for it in metal-intercalation batteries.
二维(2D)碳氮材料由于其优异的导电性和结构稳定性,已成为金属离子电池(MIBs)阳极材料的有希望的候选者。本文采用第一性原理计算方法系统地研究了C6N2在Li+/Na+/K+电池中的性能。结果表明,单层C6N2具有最佳的电子结构和优异的导电性。Li+、Na+和K+也表现出较高的吸附能,提供了稳定的吸附位点,增强了循环稳定性。对C6N2离子扩散特性的分析表明,C6N2具有较低的扩散能垒,在快速充放电循环中具有高效的性能。进一步的理论计算表明,C6N2对Li+/Na+/K+的理论比容量分别高达1596 mAh/g、1197 mAh/g和997 mAh/g,大大超过了许多传统的阳极材料。此外,它具有最小的开路电压(OCV)变化,满足电池稳定运行的要求。综上所述,C6N2优异的电化学性能和结构特点使其在金属嵌入电池中具有广阔的应用前景。
{"title":"The C6N2 monolayer as a universal anode for lithium/sodium/potassium-ion batteries: A first-principles study","authors":"Ruotong Gao ,&nbsp;Haoxiang Zhang ,&nbsp;Hai Wu ,&nbsp;XingKao Zhang ,&nbsp;Hanqing Li ,&nbsp;Xiangjie Fu ,&nbsp;Hongying Hou ,&nbsp;Ju Rong ,&nbsp;Xiaohua Yu","doi":"10.1016/j.est.2026.120902","DOIUrl":"10.1016/j.est.2026.120902","url":null,"abstract":"<div><div>Two-dimensional(2D) carbon‑nitrogen materials have emerged as promising candidates for anode materials in metal-ion batteries (MIBs) due to their exceptional electrical conductivity and structural stability. This paper employs first-principles calculations to systematically investigate the performance of C<sub>6</sub>N<sub>2</sub> in Li<sup>+</sup>/Na<sup>+</sup>/K<sup>+</sup> batteries. Results indicate that the monolayer C6N2 has an optimal electronic structure with excellent conductivity. Li+, Na+, and K+ also exhibit high adsorption energies, providing stable adsorption sites that enhance cycling stability. Analysis of C<sub>6</sub>N<sub>2</sub>'s ionic diffusion properties revealed a low diffusion energy barrier, supporting efficient performance during rapid charge-discharge cycles. Further theoretical calculations indicate that C<sub>6</sub>N<sub>2</sub> exhibits theoretical specific capacities for Li<sup>+</sup>/Na<sup>+</sup>/K<sup>+</sup> as high as 1596 mAh/g, 1197 mAh/g, and 997 mAh/g respectively, significantly surpassing many conventional anode materials. Furthermore, it exhibits minimal open-circuit voltage (OCV) variation, meeting the requirements for stable battery operation. Overall, the outstanding electrochemical performance and structural characteristics of C<sub>6</sub>N<sub>2</sub> confer broad application prospects for it in metal-intercalation batteries.</div></div>","PeriodicalId":15942,"journal":{"name":"Journal of energy storage","volume":"153 ","pages":"Article 120902"},"PeriodicalIF":8.9,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146098538","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nail penetration safety enhancement in semisolid-state batteries via composite solid-state electrolyte separators 复合固态电解质分离器增强半固态电池穿甲安全性
IF 8.9 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-04-01 Epub Date: 2026-02-02 DOI: 10.1016/j.est.2026.120847
Xingyu Yang , Dong Liang , Tao Zhang , Hailin Fan , Chongchong Zhao , Zhiwei Pan , Songwei Zhu , Feng Huo , Peigao Duan
This study develops a composite solid-state electrolyte (SSE) separator for semisolid-state batteries, achieving a 450 Wh/kg lithium metal battery that passes stringent nail penetration tests. The SSE, composed of PEO-LLZTO coated on a polypropylene base, exhibits superior elongation and ionic conductivity enabling effective nail encapsulation during penetration. A custom steel nail with embedded thermocouples was used to monitor the maximum temperature at the penetration site of different pouch cells during the nail penetration test, providing more accurate measurements than surface-mounted thermocouples. A parallel circuit model quantification demonstrated significant differences in peak current and short-circuit internal resistance between liquid batteries and semisolid-state batteries. Semisolid-state batteries with 1.4 g/Ah electrolyte filling demonstrated safety across capacities (3.2–7.5 Ah), whereas liquid batteries failed. The posttest microscope images confirmed the role of SSE in reducing the peak splitting height and fracture area of the electrodes. This work provides a methodological framework for nail penetration analysis, highlighting SSE separators as a solution to balance energy density and safety.
本研究开发了一种用于半固态电池的复合固态电解质(SSE)分离器,实现了450 Wh/kg的锂金属电池,并通过了严格的钉子穿透测试。SSE由PEO-LLZTO涂覆在聚丙烯基上,具有优异的伸长率和离子导电性,能够在穿透过程中有效地包裹钉子。采用嵌入热电偶的定制钢钉,在钉入测试中监测不同袋状细胞穿透部位的最高温度,提供比表面安装热电偶更准确的测量结果。并联电路模型量化表明,液体电池和半固态电池在峰值电流和短路内阻方面存在显著差异。充入1.4 g/Ah电解质的半固态电池在容量(3.2-7.5 Ah)范围内表现出安全性,而液体电池则失效。后测显微镜图像证实了SSE对降低电极峰劈裂高度和断裂面积的作用。这项工作为钉子穿透分析提供了一个方法论框架,强调SSE分离器是平衡能量密度和安全性的解决方案。
{"title":"Nail penetration safety enhancement in semisolid-state batteries via composite solid-state electrolyte separators","authors":"Xingyu Yang ,&nbsp;Dong Liang ,&nbsp;Tao Zhang ,&nbsp;Hailin Fan ,&nbsp;Chongchong Zhao ,&nbsp;Zhiwei Pan ,&nbsp;Songwei Zhu ,&nbsp;Feng Huo ,&nbsp;Peigao Duan","doi":"10.1016/j.est.2026.120847","DOIUrl":"10.1016/j.est.2026.120847","url":null,"abstract":"<div><div>This study develops a composite solid-state electrolyte (SSE) separator for semisolid-state batteries, achieving a 450 Wh/kg lithium metal battery that passes stringent nail penetration tests. The SSE, composed of PEO-LLZTO coated on a polypropylene base, exhibits superior elongation and ionic conductivity enabling effective nail encapsulation during penetration. A custom steel nail with embedded thermocouples was used to monitor the maximum temperature at the penetration site of different pouch cells during the nail penetration test, providing more accurate measurements than surface-mounted thermocouples. A parallel circuit model quantification demonstrated significant differences in peak current and short-circuit internal resistance between liquid batteries and semisolid-state batteries. Semisolid-state batteries with 1.4 g/Ah electrolyte filling demonstrated safety across capacities (3.2–7.5 Ah), whereas liquid batteries failed. The posttest microscope images confirmed the role of SSE in reducing the peak splitting height and fracture area of the electrodes. This work provides a methodological framework for nail penetration analysis, highlighting SSE separators as a solution to balance energy density and safety.</div></div>","PeriodicalId":15942,"journal":{"name":"Journal of energy storage","volume":"153 ","pages":"Article 120847"},"PeriodicalIF":8.9,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146098605","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Numerical simulation study of a three-dimensional multiphysics model of vanadium‑oxygen rebalance cell 钒氧再平衡电池三维多物理场模型的数值模拟研究
IF 8.9 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-04-01 Epub Date: 2026-02-14 DOI: 10.1016/j.est.2026.121074
Tangpeng Liu , Longjie Liu , Gang Xu , Yongliang Xie , Yikai Zeng
The anode of the vanadium‑oxygen rebalance cell (VORC) used for capacity recovery in vanadium flow battery faces issues such as sluggish reaction kinetics and high gas volume fraction (sg), which can affect the performance of cell and long-term operational stability. For the first time, a three-dimensional steady-state multiphysics coupled numerical model was developed for the VORC, enabling the coupling of gas-liquid flow with the cell's macroscopic performance. Based on this model, the gas-liquid phase distribution within the anode and the performance of cell under different anode flow fields and varying parameters of titanium felt could be evaluated. Numerical simulations indicated that the sgmax in the titanium felt was significantly lower when titanium mesh was employed as the anode flow field (0.129–0.165) compared to the parallel (0.486) and serpentine (0.4) flow field at 400 mA cm−2. Employing titanium mesh with smaller aperture sizes and positioning it horizontally further enhanced gas removal efficiency. To achieve satisfactory overall performance, the anode inlet flow rate must be set above 15 mL min−1 (i.e., specific flow rate was 3.75 mL min−1 cm−2) when operating at 400 mA cm−2. Utilizing a porous titanium felt featuring a smaller contact angle and higher porosity also significantly improved liquid saturation. This research can provide references for the future design of high-performance, durable VORCs and the establishment of more comprehensive and accurate numerical models for VORCs.
用于钒液流电池容量回收的钒氧再平衡电池(VORC)阳极存在反应动力学缓慢、气体体积分数(sg)过高等问题,影响电池性能和长期运行稳定性。首次建立了旋涡管的三维稳态多物理场耦合数值模型,实现了气液流动与电池宏观性能的耦合。基于该模型,可以对不同阳极流场和不同钛毡参数下阳极内气液相分布及电池性能进行评价。数值模拟结果表明,在400 mA cm−2时,钛网作为阳极流场(0.129 ~ 0.165)时,钛毡中的sgmax明显低于平行流场(0.486)和蛇形流场(0.4)。采用孔径较小的钛网水平定位,进一步提高了除气效率。为了达到令人满意的整体性能,阳极进口流量必须设置在15 mL min - 1以上(即,当工作在400 mA cm - 2时,比流量为3.75 mL min - 1 cm - 2)。利用多孔钛毡具有更小的接触角和更高的孔隙率也显著提高了液体饱和度。该研究可为今后设计高性能、耐用的涡流涡流控制系统以及建立更全面、准确的涡流涡流控制系统数值模型提供参考。
{"title":"Numerical simulation study of a three-dimensional multiphysics model of vanadium‑oxygen rebalance cell","authors":"Tangpeng Liu ,&nbsp;Longjie Liu ,&nbsp;Gang Xu ,&nbsp;Yongliang Xie ,&nbsp;Yikai Zeng","doi":"10.1016/j.est.2026.121074","DOIUrl":"10.1016/j.est.2026.121074","url":null,"abstract":"<div><div>The anode of the vanadium‑oxygen rebalance cell (VORC) used for capacity recovery in vanadium flow battery faces issues such as sluggish reaction kinetics and high gas volume fraction (<em>s</em><sub><em>g</em></sub>), which can affect the performance of cell and long-term operational stability. For the first time, a three-dimensional steady-state multiphysics coupled numerical model was developed for the VORC, enabling the coupling of gas-liquid flow with the cell's macroscopic performance. Based on this model, the gas-liquid phase distribution within the anode and the performance of cell under different anode flow fields and varying parameters of titanium felt could be evaluated. Numerical simulations indicated that the <em>s</em><sub><em>gmax</em></sub> in the titanium felt was significantly lower when titanium mesh was employed as the anode flow field (0.129–0.165) compared to the parallel (0.486) and serpentine (0.4) flow field at 400 mA cm<sup>−2</sup>. Employing titanium mesh with smaller aperture sizes and positioning it horizontally further enhanced gas removal efficiency. To achieve satisfactory overall performance, the anode inlet flow rate must be set above 15 mL min<sup>−1</sup> (i.e., specific flow rate was 3.75 mL min<sup>−1</sup> cm<sup>−2</sup>) when operating at 400 mA cm<sup>−2</sup>. Utilizing a porous titanium felt featuring a smaller contact angle and higher porosity also significantly improved liquid saturation. This research can provide references for the future design of high-performance, durable VORCs and the establishment of more comprehensive and accurate numerical models for VORCs.</div></div>","PeriodicalId":15942,"journal":{"name":"Journal of energy storage","volume":"153 ","pages":"Article 121074"},"PeriodicalIF":8.9,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146171855","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Profitable and reliable EV charging infrastructure: A time-series power flow model for improved voltage and power stability 可盈利且可靠的电动汽车充电基础设施:用于改善电压和功率稳定性的时间序列功率流模型
IF 8.9 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-04-01 Epub Date: 2026-02-12 DOI: 10.1016/j.est.2026.120923
M. Senthilkumar , R. Saravanan , V. Madhu Kumar , G.G. Raja Sekhar
Efficient and sustainable planning of Electric Vehicle (EV) charging infrastructure requires balancing technical, economic, and environmental factors. Existing EV Charging Station (EVCS) designs often overlook user convenience and grid reliability, while failing to account for uncertainties, which can lead to inefficiencies and suboptimal system performance. This study presents an intelligent approach for profitable and reliable EV charging infrastructure using a Time-Series Power Flow (TSPF) model to enhance voltage and power stability. The proposed method integrates the Opposition-Based Botox Optimization Algorithm (OBOA) and Spatio-Temporal Field Neural Network (STFNN), referred to as the OBOA-STFNN technique. The BOA optimizes the siting and sizing of EVCSs to balance operator profit, grid stability, and user convenience, while STFNN predicts individual EV charging behavior and station demand. The effectiveness of the technique is evaluated in MATLAB and compared with Particle Swarm Optimization (PSO), Modified Snake Optimization (MSO), and Convolutional Neural Network (CNN) approaches. Simulation results demonstrate that the OBOA-STFNN method significantly reduces energy consumption to 38.74 MWh and energy loss to 418 MWh, while achieving a lower optimal cost, mean, and standard deviation, along with reduced total computation time. These results highlight the superior efficiency, reliability, and practicality of the proposed approach for EVCS planning and operation.
高效、可持续的电动汽车充电基础设施规划需要平衡技术、经济和环境因素。现有的电动汽车充电站(EVCS)设计往往忽视了用户的便利性和电网的可靠性,同时未能考虑到不确定性,这可能导致效率低下和系统性能不佳。本研究提出了一种利用时序功率流(TSPF)模型来提高电压和功率稳定性的智能方法,以实现有利可图和可靠的电动汽车充电基础设施。该方法将基于对立的肉毒杆菌优化算法(OBOA)与时空场神经网络(STFNN)相结合,称为OBOA-STFNN技术。BOA优化电动汽车充电站的选址和规模,以平衡运营商利润、电网稳定性和用户便利性,而STFNN预测单个电动汽车充电行为和充电站需求。在MATLAB中对该方法的有效性进行了评估,并与粒子群优化(PSO)、改进蛇优化(MSO)和卷积神经网络(CNN)方法进行了比较。仿真结果表明,oba - stfnn方法显著降低能耗至38.74 MWh,能量损失至418 MWh,同时实现了较低的最优成本、均值和标准差,并减少了总计算时间。这些结果突出了该方法在EVCS规划和运行方面的卓越效率、可靠性和实用性。
{"title":"Profitable and reliable EV charging infrastructure: A time-series power flow model for improved voltage and power stability","authors":"M. Senthilkumar ,&nbsp;R. Saravanan ,&nbsp;V. Madhu Kumar ,&nbsp;G.G. Raja Sekhar","doi":"10.1016/j.est.2026.120923","DOIUrl":"10.1016/j.est.2026.120923","url":null,"abstract":"<div><div>Efficient and sustainable planning of Electric Vehicle (EV) charging infrastructure requires balancing technical, economic, and environmental factors. Existing EV Charging Station (EVCS) designs often overlook user convenience and grid reliability, while failing to account for uncertainties, which can lead to inefficiencies and suboptimal system performance. This study presents an intelligent approach for profitable and reliable EV charging infrastructure using a Time-Series Power Flow (TSPF) model to enhance voltage and power stability. The proposed method integrates the Opposition-Based Botox Optimization Algorithm (OBOA) and Spatio-Temporal Field Neural Network (STFNN), referred to as the OBOA-STFNN technique. The BOA optimizes the siting and sizing of EVCSs to balance operator profit, grid stability, and user convenience, while STFNN predicts individual EV charging behavior and station demand. The effectiveness of the technique is evaluated in MATLAB and compared with Particle Swarm Optimization (PSO), Modified Snake Optimization (MSO), and Convolutional Neural Network (CNN) approaches. Simulation results demonstrate that the OBOA-STFNN method significantly reduces energy consumption to 38.74 MWh and energy loss to 418 MWh, while achieving a lower optimal cost, mean, and standard deviation, along with reduced total computation time. These results highlight the superior efficiency, reliability, and practicality of the proposed approach for EVCS planning and operation.</div></div>","PeriodicalId":15942,"journal":{"name":"Journal of energy storage","volume":"153 ","pages":"Article 120923"},"PeriodicalIF":8.9,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146171860","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A distributed optimization method for wind-storage systems with superlinear convergence 风电系统超线性收敛的分布式优化方法
IF 8.9 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2026-04-01 Epub Date: 2026-02-12 DOI: 10.1016/j.est.2026.121035
Xiuyan Guo , Qi Liu , Yeming Xu , Liping Zhang , Xiao Lu
Distributed energy storage systems have been widely deployed to mitigate power generation fluctuations from wind farm clusters due to their flexible regulation capability. Distributed optimization is well-suited for managing these systems because of its lower communication overhead and enhanced robustness. However, conventional distributed methods often suffer from low computational efficiency and slow convergence. To address these limitations, this paper proposes a novel distributed optimization method that achieves both low communication costs and superlinear convergence. First, a bi-level optimization model is developed for wind-storage systems, incorporating global–local power coordination, equipment life-cycle cost, and the relative carbon payback period. The payback period is formulated using a high-order Taylor series expansion to enhance numerical accuracy. Secondly, a distributed optimization algorithm based on optimal control theory is proposed. By leveraging Pontryagin’s maximum principle and forward–backward difference equations, the method avoids Hessian inversion while guaranteeing this accelerated convergence rate. Finally, comprehensive simulations verify that the proposed approach reduces carbon emissions and enhances system robustness. Compared to the distributed gradient descent and network Newton algorithms, the proposed method achieves computational efficiency that is 2.92 and 51.37 times higher, respectively, while also improving solution accuracy.
分布式储能系统由于其灵活的调节能力,已被广泛应用于缓解风力发电场集群的发电波动。分布式优化非常适合管理这些系统,因为它具有较低的通信开销和增强的健壮性。然而,传统的分布式算法存在计算效率低、收敛速度慢的问题。为了解决这些限制,本文提出了一种新的分布式优化方法,既能实现低通信成本,又能实现超线性收敛。首先,建立了考虑全局-局部电力协调、设备全寿命周期成本和相对碳回收期的风电系统双层优化模型。投资回收期采用高阶泰勒级数展开式来提高数值精度。其次,提出了基于最优控制理论的分布式优化算法。该方法利用Pontryagin的极大值原理和前后向差分方程,在保证加速收敛速度的同时避免了Hessian反演。最后,综合仿真验证了该方法降低了碳排放,增强了系统的鲁棒性。与分布式梯度下降算法和网络牛顿算法相比,该方法的计算效率分别提高了2.92倍和51.37倍,同时也提高了求解精度。
{"title":"A distributed optimization method for wind-storage systems with superlinear convergence","authors":"Xiuyan Guo ,&nbsp;Qi Liu ,&nbsp;Yeming Xu ,&nbsp;Liping Zhang ,&nbsp;Xiao Lu","doi":"10.1016/j.est.2026.121035","DOIUrl":"10.1016/j.est.2026.121035","url":null,"abstract":"<div><div>Distributed energy storage systems have been widely deployed to mitigate power generation fluctuations from wind farm clusters due to their flexible regulation capability. Distributed optimization is well-suited for managing these systems because of its lower communication overhead and enhanced robustness. However, conventional distributed methods often suffer from low computational efficiency and slow convergence. To address these limitations, this paper proposes a novel distributed optimization method that achieves both low communication costs and superlinear convergence. First, a bi-level optimization model is developed for wind-storage systems, incorporating global–local power coordination, equipment life-cycle cost, and the relative carbon payback period. The payback period is formulated using a high-order Taylor series expansion to enhance numerical accuracy. Secondly, a distributed optimization algorithm based on optimal control theory is proposed. By leveraging Pontryagin’s maximum principle and forward–backward difference equations, the method avoids Hessian inversion while guaranteeing this accelerated convergence rate. Finally, comprehensive simulations verify that the proposed approach reduces carbon emissions and enhances system robustness. Compared to the distributed gradient descent and network Newton algorithms, the proposed method achieves computational efficiency that is 2.92 and 51.37 times higher, respectively, while also improving solution accuracy.</div></div>","PeriodicalId":15942,"journal":{"name":"Journal of energy storage","volume":"153 ","pages":"Article 121035"},"PeriodicalIF":8.9,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146171883","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of energy storage
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1