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Impact of Aerogel Barrier on Liquid-Cooled Lithium-Ion Battery Thermal Management System's Cooling Efficiency 气凝胶屏障对液冷式锂离子电池热管理系统冷却效率的影响
IF 3.6 4区 工程技术 Q3 ENERGY & FUELS Pub Date : 2024-08-30 DOI: 10.1002/ente.202400923
Keyi Zeng, Ying Zhang, Liyu Tian, Zengyan Lai, Liang Zhu, Chuyuan Ma

Thermal runaway propagation (TRP) in lithium batteries poses significant risks to energy-storage systems. Therefore, it is necessary to incorporate insulating materials between the batteries to prevent the TRP. However, the incorporation of insulating materials will impact the battery thermal management system (BTMS). In this article, the influence of aerogel insulation on liquid-cooled BTMS is analyzed employing experiments and simulations. In the experiment results, it is revealed that aerogel reduces heat dissipation from liquid-cooled battery packs, leading to elevated peak temperatures and steeper temperature gradients. Simulation of battery pack discharge warming based on the 3D model shows that the result matches very well with that in the experiment., indicating a maximum temperature rise from 34.92 to 42.57 °C at 2C when aerogel thickness is increased to 5 mm, alongside a temperature differential expansion from 11.11 to 17.50 °C. Nonetheless, beyond 3 mm thickness, further increases in aerogel thickness cause negligible (<0.1 °C) temperature alterations, defining the saturation thickness of aerogel. Furthermore, maintaining consistent thickness and stacking more aerogel layers do not mitigate its detrimental effects. Interestingly, augmenting the battery's through-thickness thermal conductivity counteracts the adverse outcomes of aerogel usage.

锂电池的热失控传播(TRP)对储能系统构成重大风险。因此,有必要在电池之间采用绝缘材料来防止 TRP。然而,加入绝缘材料会对电池热管理系统(BTMS)产生影响。本文通过实验和模拟分析了气凝胶绝缘材料对液冷电池热管理系统的影响。实验结果表明,气凝胶可减少液冷电池组的散热,从而导致峰值温度升高和温度梯度增大。基于三维模型的电池组放电升温模拟显示,结果与实验结果非常吻合,表明当气凝胶厚度增加到5毫米时,2℃时的最高温度从34.92℃上升到42.57℃,同时温差从11.11℃扩大到17.50℃。然而,厚度超过 3 毫米后,气凝胶厚度的进一步增加引起的温度变化可以忽略不计(0.1 °C),从而确定了气凝胶的饱和厚度。此外,保持一致的厚度和堆叠更多的气凝胶层并不能减轻其不利影响。有趣的是,提高电池的厚度导热性可以抵消气凝胶的不利影响。
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引用次数: 0
Unlocking the Impact of “Cell Position” on Solid-State Hydrogen Storage: Investigations on an Activated Carbon Electrode Integrated in a Modified Reversible Polymer Electrolyte Membrane Fuel Cell 揭示 "电池位置 "对固态储氢的影响:对集成在改良可逆聚合物电解质膜燃料电池中的活性炭电极的研究
IF 3.6 4区 工程技术 Q3 ENERGY & FUELS Pub Date : 2024-08-30 DOI: 10.1002/ente.202400215
Rupinder Singh, Amandeep Singh Oberoi, Talwinder Singh

The presented maiden experimental study introduces a novel cell position concept for a modified reversible polymer electrolyte membrane fuel cell with an integrated hydrogen storage (H-storage) electrode. The primary focus of the current study is to enhance the H-storage capacity of a carbon-based self-standing electrode by testing it in vertical, horizontally upward, and horizontally downward positions to meet U.S. Department of Energy objectives. The results show that the developed cell achieves the highest electrochemical hydrogen adsorption (H-adsorption) of 1.3 weight percent (wt%) in the horizontal downward position during charging, surpassing the vertical position by 36.1% and outperforming the horizontal upward position by 25.3%. The reversible rates of stored hydrogen are measured as 0.587 wt% in the vertical position, 0.781 wt% in the horizontal upward position, and 0.998 wt% in the horizontal downward position. The cell manages to deliver a peak output of 2.2 V and a maximum current of 0.5 mA during the initial discharging phase. The insights gained from this study on cell positioning are poised to inspire future research efforts aimed at enhancing hydrogen storage capacity and its reversibility.

这项首次实验研究为带有集成储氢(H-storage)电极的改良型可逆聚合物电解质膜燃料电池引入了一种新的电池位置概念。当前研究的主要重点是通过在垂直、水平向上和水平向下位置进行测试,提高碳基自立式电极的储氢能力,以实现美国能源部的目标。结果表明,所开发的电池在水平向下位置充电时的电化学吸氢率(H-adsorption)最高,达到 1.3 重量百分比(wt%),比垂直位置高出 36.1%,比水平向上位置高出 25.3%。据测量,垂直位置的可逆储氢率为 0.587 重量%,水平向上位置为 0.781 重量%,水平向下位置为 0.998 重量%。在初始放电阶段,电池能输出 2.2 V 的峰值电压和 0.5 mA 的最大电流。这项研究在电池定位方面获得的启示,将激励未来旨在提高储氢能力及其可逆性的研究工作。
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引用次数: 0
Performance Analysis of the Outdoor Concentrating Photovoltaic–Thermoelectric Coupling System Under Uniform Illumination 室外聚光光伏热电耦合系统在均匀光照下的性能分析
IF 3.6 4区 工程技术 Q3 ENERGY & FUELS Pub Date : 2024-08-30 DOI: 10.1002/ente.202400779
Xiaoxiao Yu, Xiaoxue Guo, Yuanyuan Wang, Lan Dong, Zhenbo Wang, Zihua Wu, Huaqing Xie

Concentrating photovoltaic–thermoelectric (CPV–TE) coupling system is an efficient solar-to-electric technology, but the nonuniform illumination and temperature caused by the concentrated light have a significant impact on the power generation performance of the cell. This work improves the intensity distribution through the self-made birefringent prism, and further studies the effect of uniform or nonuniform illumination on the power generation performance of CPV–TE system under different light intensities and cooling conditions. The results show that the output power of PV cell at uniform illumination can achieve 14.74% higher than that at nonuniform illumination due to the decline of cell’ surface temperature difference. Meanwhile, the cooling condition can further enhance the output power of PV or TE cell, and weakens the impact of the illumination nonuniformity on the power generation performance of PV cell. Through the joint optimization of uniform illumination and 10 °C cooling condition, CPV–TE coupling system increases the output power by 15.83% at 10 kW m2. TE device can further enhance the output power by 46.09 mW through the thermoelectric conversion. Surprisingly, the environmental cost from CPV–TE system reduces carbon dioxide emission of 26471.01¥ m−2 every day. The outdoor CPV–TE coupling system has a certain assistance for the practical development.

聚光光伏热电(CPV-TE)耦合系统是一种高效的太阳能发电技术,但聚光引起的不均匀光照和温度对电池的发电性能有很大影响。本研究通过自制双折射棱镜改善了光强分布,并进一步研究了在不同光强和冷却条件下,均匀或不均匀光照对 CPV-TE 系统发电性能的影响。结果表明,在均匀光照条件下,由于电池表面温差的减小,光伏电池的输出功率比非均匀光照条件下提高了 14.74%。同时,冷却条件可以进一步提高 PV 或 TE 电池的输出功率,削弱光照不均匀性对 PV 电池发电性能的影响。通过对均匀光照和 10 °C 冷却条件的联合优化,CPV-TE 耦合系统在 10 kW m-2 时的输出功率提高了 15.83%。TE 设备通过热电转换可进一步提高输出功率 46.09 mW。令人惊讶的是,CPV-TE 系统的环境成本减少了每天 26471.01¥ m-2 的二氧化碳排放量。室外 CPV-TE 耦合系统对实际发展有一定的帮助。
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引用次数: 0
Optimizing Solar Cell Performance: Hybrid Planar-Si/Organic Heterojunction Solar Cells Achieve 14.75% Efficiency Through Dibenzothiophene-Spirobifluorene-Dithienothiophene Insertion Layer Integration 优化太阳能电池性能:通过整合二苯并噻吩-螺二芴-二硫代噻吩插入层,平面硅/有机杂质结混合太阳能电池实现 14.75% 的效率
IF 3.6 4区 工程技术 Q3 ENERGY & FUELS Pub Date : 2024-08-30 DOI: 10.1002/ente.202401249
Fahim Ullah, Kamran Hasrat, Sami Iqbal, Shuang Wang

Hybrid planar-Si/organic heterojunction solar cells have garnered substantial interest due to their potential for producing cost-effective, high-efficiency devices. This study investigates the photophysical properties and application of dibenzothiophene-spirobifluorene-dithienothiophene (DBBT-mCbz-DBT) in enhancing the efficiency of photovoltaic devices. Utilizing ultraviolet–visible and fluorescence spectroscopy, DBBT-mCbz-DBT is analyzed in solutions and doped films, showing maximum absorption at 380 nm and emission at 440 nm. Notably, the photoluminescence intensity in 4,4′-di(9H-carbazol-9-yl)-1,1′-biphenyl films peaks at 40–50% DBBT-mCbz-DBT concentrations, which are selected for solar cell fabrication. Enhanced light absorption and charge transport are observed with a DBBT-mCbz-DBT layer on silicon, significantly improving device performance. The planar silicon/poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) (Si/PEDOT:PSS) heterojunction solar cells with DBBT-mCbz-DBT exhibit a power conversion efficiency of 14.75%, demonstrating substantial gains over baseline structures. The DBBT-mCbz-DBT layer optimizes energy band alignment, reduces recombination losses, and enhances electron transport, improving overall device efficiency. This research underscores the potential of integrating DBBT-mCbz-DBT in solar cells to achieve higher performance through simple, scalable fabrication methods.

平面硅/有机杂结混合太阳能电池因其具有生产高性价比、高效率器件的潜力而备受关注。本研究探讨了二苯并噻吩-螺二芴-二噻吩(DBBT-mCbz-DBT)的光物理性质及其在提高光伏设备效率方面的应用。利用紫外可见光谱和荧光光谱分析了溶液和掺杂薄膜中的 DBBT-mCbz-DBT,结果表明其在 380 纳米处有最大吸收,在 440 纳米处有最大发射。值得注意的是,4,4′-二(9H-咔唑-9-基)-1,1′-联苯薄膜中的光致发光强度在 DBBT-mCbz-DBT 浓度为 40-50% 时达到峰值,可用于太阳能电池的制造。硅上的 DBBT-mCbz-DBT 层可增强光吸收和电荷传输,从而显著提高设备性能。含有 DBBT-mCbz-DBT 的平面硅/聚(3,4-乙烯二氧噻吩):聚(苯乙烯磺酸)(Si/PEDOT:PSS)异质结太阳能电池的功率转换效率达到 14.75%,与基线结构相比有了大幅提高。DBBT-mCbz-DBT 层优化了能带排列,降低了重组损耗,增强了电子传输,从而提高了器件的整体效率。这项研究强调了在太阳能电池中集成 DBBT-mCbz-DBT 的潜力,通过简单、可扩展的制造方法实现更高的性能。
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引用次数: 0
High Entropy Alloys: Emerging Materials for Advanced Hydrogen Storage 高熵合金:先进储氢的新兴材料
IF 3.6 4区 工程技术 Q3 ENERGY & FUELS Pub Date : 2024-08-30 DOI: 10.1002/ente.202401061
Yi Jiang, Wei Jiang

High entropy alloys (HEAs) have attracted substantial attention in diverse fields, including hydrogen storage, owing to their unique structural and functional properties. The diverse components of HEAs have made them a focal point in research, aiming to develop new hydrogen storage materials with exceptional comprehensive properties. The present study provides a comprehensive review of the research progress in the hydrogen storage technology of HEAs. It covers microstructure analysis, theoretical calculations, hydrogen storage performance evaluation, and other pertinent applications. Furthermore, this paper introduces diverse hydrogen-related applications while also addressing the current challenges and issues faced by researchers in the field of HEAs for hydrogen storage technology.

高熵合金(HEAs)因其独特的结构和功能特性,在包括储氢在内的多个领域引起了广泛关注。高熵合金的各种成分使其成为研究的焦点,目的是开发具有特殊综合性能的新型储氢材料。本研究全面回顾了 HEAs 储氢技术的研究进展。研究内容包括微观结构分析、理论计算、储氢性能评估以及其他相关应用。此外,本文还介绍了与氢有关的各种应用,同时也探讨了当前氢能源效率材料储氢技术领域的研究人员所面临的挑战和问题。
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引用次数: 0
Synthesis of Co–ZnAl‐Layered Double Hydroxide for Effective Activation of Peroxymonosulfate to Degrade Rhodamine B and Methyl Orange from Polluted Water 合成共锌铝层双氢氧化物,以有效活化过一硫酸盐,从而降解污染水中的罗丹明 B 和甲基橙
IF 3.8 4区 工程技术 Q3 ENERGY & FUELS Pub Date : 2024-08-29 DOI: 10.1002/ente.202401293
Hafiza Mehwish Rasheed, Chunsheng Ding, Minghua Xu, Bilal Zaman, Xiaowen Ruan, Xiaoqiang Cui
Innovative technologies based on the sulfate radical advanced oxidation process are attracting more attention for the degradation of dyes in impure water. Herein, cobalt‐doped zinc aluminum layered double hydroxide (LDH) catalysts are synthesized based on the assembly of LDHs for efficient activation of peroxymonosulfate and simultaneous catalytic degradation of rhodamine B (RhB) and methyl orange (MO). Cobalt metal is incorporated into the ZnAl‐LDH lattice to accelerate the catalytic performance of ZnAl‐LDHs. The experimental results show that the Co–ZnAl‐LDH (Co = 0.05 mmol) system demonstrates remarkable degradation of RhB and MO with maximum degradation efficiencies of 98.97% and 98.04%, respectively, through the attack of reactive oxygen species and electron transfer processes. Furthermore, the structural stability and catalytic performance of the catalyst make it promising for practical water treatment as well as promoting its reuse ability.
基于硫酸根高级氧化过程的创新技术在降解不纯净水中的染料方面受到越来越多的关注。本文在组装 LDH 的基础上合成了掺钴锌铝层状双氢氧化物(LDH)催化剂,用于高效活化过一硫酸盐并同时催化降解罗丹明 B(RhB)和甲基橙(MO)。金属钴被加入到 ZnAl-LDH 晶格中,以加速 ZnAl-LDH 的催化性能。实验结果表明,Co-ZnAl-LDH(Co = 0.05 mmol)体系通过活性氧的攻击和电子转移过程,对 RhB 和 MO 的降解效果显著,最大降解效率分别为 98.97% 和 98.04%。此外,该催化剂的结构稳定性和催化性能使其在实际水处理中大有可为,并提高了其再利用能力。
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引用次数: 0
Recent Progresses of Battery Thermal Management Systems Based on Phase Change Materials 基于相变材料的电池热管理系统的最新进展
IF 3.6 4区 工程技术 Q3 ENERGY & FUELS Pub Date : 2024-08-29 DOI: 10.1002/ente.202400563
Changren Xiao, Jiangyun Zhang, Guoqing Zhang, Chengzhao Yang, Wenzhao Jiang, Youpeng Chen, Chaoqun Tu

Battery thermal management system (BTMS) based on phase change materials (PCMs) is simple in structure while presenting outstanding performance, but the core bottleneck hindering the industrialization of which is the poor performance of PCMs’ pivotal properties. Apart from that, under extreme conditions, single passive phase change temperature-control technology apparently could not meet the demands. Therefore, modification strategies to improve PCM's pivotal properties suitable for BTMS are thoroughly reviewed. Moreover, the optimization of as-mentioned passive systems by integrating them with other active heating or cooling devices to obtain advanced active and passive full-temperature responsive capability is also summarized. Profound opinions concerning about the prospect and challenges of PCM-BTMS are given. It is expected to provide some innovative ideas for the advancement of such promising technology.

基于相变材料(PCMs)的电池热管理系统(BTMS)结构简单、性能卓越,但其产业化的核心瓶颈在于 PCMs 的关键性能不佳。此外,在极端条件下,单一的被动相变温控技术显然无法满足需求。因此,本文深入探讨了适合 BTMS 的 PCM 关键性能改进策略。此外,还总结了通过与其他主动加热或冷却装置集成来优化上述被动系统,从而获得先进的主动和被动全温度响应能力。对 PCM-BTMS 的前景和挑战提出了深刻的见解。希望能为这种前景广阔的技术的发展提供一些创新思路。
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引用次数: 0
Co–Mn Bimetallic Metal–Organic Frameworks Nanosheets for Efficient Oxygen Evolution Electrocatalysis 用于高效氧进化电催化的 Co-Mn 双金属金属有机框架纳米片
IF 3.6 4区 工程技术 Q3 ENERGY & FUELS Pub Date : 2024-08-27 DOI: 10.1002/ente.202401049
Yongchao Hao, Ling Wang, Shuling Cheng, Huiya Cheng, Qianyun He, Lizhi Yi

Developing an efficient oxygen evolution reaction (OER) catalyst is the footstone of many electrochemical energy conversion devices. Herein, a cobalt–manganese bimetallic metal–organic framework (MOF) is developed as an efficient OER catalyst (denoted as Co3Mn1 BDC). The Co3Mn1 BDC nanosheets demonstrate advantages in specific surface area, pore size distribution comparing with monometallic Co BDC and Mn BDC. The performance investigations demonstrate that the doping of Mn in Co-based MOFs facilitates the electrochemical area, charge transfer efficiency, reaction kinetics, and turnover frequency. As a consequence, the Co3Mn1 BDC exhibits a low overpotential of 289 mV at current of 10 mA cm−2 and a favorable Tafel slope of 56.8 mV dec−1 on glassy carbon electrode, which is better than IrO2. When the catalyst is loaded on Ni foam, the overpotential and Tafel slope are further decreased to 231 mV and 50.8 mV dec−1. Moreover, the Raman spectrum confirms that the Co3Mn1 BDC can be transformed into active CoOOH, suggesting the bright prospect in electrocatalysis devices as “precatalyst”.

开发高效的氧进化反应(OER)催化剂是许多电化学能量转换装置的基础。在此,我们开发了一种钴锰双金属金属有机框架(MOF)作为高效氧进化反应催化剂(简称为 Co3Mn1 BDC)。与单金属 Co BDC 和 Mn BDC 相比,Co3Mn1 BDC 纳米片在比表面积和孔径分布方面具有优势。性能研究表明,在 Co 基 MOF 中掺入 Mn 有助于提高电化学面积、电荷转移效率、反应动力学和翻转频率。因此,当电流为 10 mA cm-2 时,Co3Mn1 BDC 的过电位低至 289 mV,在玻璃碳电极上的 Tafel 斜坡为 56.8 mV dec-1,优于 IrO2。当催化剂负载在泡沫镍上时,过电位和塔菲尔斜率进一步下降到 231 mV 和 50.8 mV dec-1。此外,拉曼光谱证实 Co3Mn1 BDC 可转化为活性 CoOOH,这表明其作为 "前催化剂 "在电催化装置中具有广阔的应用前景。
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引用次数: 0
Predicting the Gas Storage Capacity in Shale Formations Using the Extreme Gradient Boosting Decision Trees Method 利用极端梯度提升决策树方法预测页岩层的天然气存储容量
IF 3.6 4区 工程技术 Q3 ENERGY & FUELS Pub Date : 2024-08-27 DOI: 10.1002/ente.202400377
Jiaheng Wang, Nong Li, Xiangyu Huo, Mingli Yang, Li Zhang

Accurate shale gas reserves estimation is essential for development. Existing machine learning (ML) models for predicting gas isothermal adsorption are limited by small datasets and lack verified generalization. We constructed an “original dataset” containing 2112 data points from 11 measurements on samples from 8 formations in 3 countries to develop ML-based prediction models. Similar to previous ML models, total organic matter, pressure, and temperature are characterized as the three most significant features using the mean impurity method. In contrast to previous ML models, the study reveals that these three features are inadequate to be used to make reasonable predictions for the datasets from the measurements different from those used to train the models. Instead, the extreme gradient boosting decision trees (XGBoost) model with two more features (specific surface area and moisture) exhibits good robustness, generalization, and precision in the prediction of gas isothermal adsorption. Overall, An XGBoost model with optimal input features is developed in this work, which exhibits both good performance in gas adsorption prediction and good potential for the estimation of gas storage in shale gas development.

准确估算页岩气储量对开发至关重要。用于预测天然气等温吸附的现有机器学习(ML)模型受限于数据集较小,且缺乏经过验证的通用性。我们构建了一个 "原始数据集",其中包含来自 3 个国家 8 个地层样本的 11 次测量的 2112 个数据点,用于开发基于 ML 的预测模型。与以往的 ML 模型类似,使用平均杂质法将总有机质、压力和温度作为三个最重要的特征。与以往的 ML 模型不同的是,研究发现这三个特征不足以用来对来自不同于用于训练模型的测量数据集进行合理预测。相反,带有另外两个特征(比表面积和水分)的极端梯度提升决策树(XGBoost)模型在预测气体等温吸附时表现出良好的鲁棒性、泛化和精确性。总之,本研究建立了一个具有最佳输入特征的 XGBoost 模型,该模型在气体吸附预测中表现出了良好的性能,在页岩气开发中的气体储量估算方面也具有良好的潜力。
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引用次数: 0
Modeling and Optimizing the Drying Process of Electrode Manufacturing for Lithium-Ion Batteries 锂离子电池电极制造干燥过程的建模与优化
IF 3.6 4区 工程技术 Q3 ENERGY & FUELS Pub Date : 2024-08-26 DOI: 10.1002/ente.202401146
Yuxin Chen, Haolan Tao, Bing Li, Baorong Li, Cheng Lian, Honglai Liu

Drying the electrode is a crucial process in the manufacture of lithium-ion batteries, which significantly affects the mechanical performance and cycle life of electrodes. High drying rate increases the battery production but reduces the uniformity of the binder in the electrode, which causes the detaching of the electrode from the collector. Herein, a physical model that couples solvent evaporation and binder diffusion is established to study the uneven enrichment of binder during the drying process. The results indicate that the drying process at the high solvent partial pressure and in a temperature-drop situation ensures sufficient time for the diffusion of binder, which breaks the trade-off between drying efficiency and electrode quality. Based on a comprehensive correlation analysis between process parameters and drying performance, an empirical equation is established to predict binder distribution. This work could offer insights into the formation and evolution of binder enrichment in electrodes and potentially provide guidelines for optimizing the drying processes of electrode.

电极干燥是锂离子电池制造过程中的一道关键工序,会对电极的机械性能和循环寿命产生重大影响。高干燥速率会提高电池产量,但会降低电极中粘结剂的均匀性,从而导致电极与集电体分离。本文建立了一个将溶剂蒸发和粘结剂扩散结合起来的物理模型,以研究干燥过程中粘结剂的不均匀富集。结果表明,在高溶剂分压和温度下降的情况下,干燥过程可确保粘结剂有足够的扩散时间,从而打破了干燥效率和电极质量之间的权衡。基于工艺参数和干燥性能之间的综合相关分析,建立了一个经验方程来预测粘合剂的分布。这项工作有助于深入了解电极中粘结剂富集的形成和演变过程,并有可能为优化电极干燥过程提供指导。
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引用次数: 0
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