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Thermoelectric Characteristics of Bulk Cr2Te3 with Low Lattice Thermal Conductivity 低点阵热导率大块Cr2Te3的热电特性
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-25 DOI: 10.1007/s13391-024-00523-x
Donghyun Shin, Hyunji Kim, Joseph Ngugi Kahiu, Samuel Kimani Kihoi, Ho Seong Lee

In this study, we aimed to synthesize bulk Cr2Te3 and evaluate its thermoelectric properties. Previously, Cr2Te3 with a layered structure has primarily been synthesized in thin film form for studies that focused on its magnetic properties. The intrinsic layered structure of Cr₂Te₃ can contributes to its low lattice thermal conductivity. Our experimental results confirmed the successful synthesis of a homogeneous single-phase specimen and revealed a significantly low lattice thermal conductivity of 0.31 W/mK at 673 K. Additionally, we explored the substitution of titanium and germanium at chromium sites as a method to enhance thermoelectric performance, achieving a notable increase in the power factor.

Graphical Abstract

在这项研究中,我们的目的是合成块状的Cr2Te3,并评估其热电性能。在此之前,层状结构的Cr2Te3主要以薄膜形式合成,主要用于研究其磁性。Cr₂Te₃固有的层状结构有助于其低晶格导热系数。我们的实验结果证实了均匀单相样品的成功合成,并且在673 K时晶格热导率显著降低,为0.31 W/mK。此外,我们探索了钛和锗在铬位点的替代,作为一种提高热电性能的方法,实现了功率因数的显着增加。图形抽象
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引用次数: 0
Multi-Functional Molybdenum Oxide Doping to Improve the Electrical Characteristics of Indium Oxide Thin Film Transistors 多功能氧化钼掺杂改善氧化铟薄膜晶体管电特性
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-24 DOI: 10.1007/s13391-024-00522-y
Kwan-Jun Heo, Jae-Yun Lee, Gergely Tarsoly, Sung-Jin Kim

This study investigates the utilization of MoO3 precursors to enhance the electrical properties and stability of In2O3 TFTs based on eco-friendly aqueous solutions. Specifically, MoO3 doped In2O3 (Mo-In2O3) TFTs were examined in this research. The Mo cation, hydroxide anion, and oxide radical of the MoO3 precursor provide free electrons to the In2O3 thin film, reducing the trap site between the semiconductor interface, the semiconductor and the insulator, and improving the stability of the device by adjusting the oxygen vacancy. To verify the change in the electrical properties of In2O3 TFT due to MoO3 doping, measurements of electron mobility after 30 days confirmed that In2O3 TFT electron mobility decreased by more than 80%, whereas Mo-In2O3 TFT electron mobility remained stable. PBS and NBS reliability evaluations confirmed that the Vth change of Mo- In2O3 TFT was less than that of In2O3 TFT. (In2O3 TFT PBS: 5.55 V, NBS: 0.33 V, Mo-In2O3 TFT PBS: 4.04 V, NBS: 0.10 V). In order to confirm the interface change of In2O3 film according to MoO3 Doping, the difference in surface roughness was measured using an AFM and found to be within 4%. In addition, the doping effect of the active layer was verified through changes in oxygen species in XPS analysis. To demonstrate its application as an active electronic device, a Mo-In2O3 TFT based resistance load inverter was evaluated, and the voltage transfer curve and excellent inversion characteristics of the inverter were confirmed under various VDD conditions.

Graphical Abstract

Kwan-Jun Heo et al., multi-functional molybdenum oxide doping to improve the electrical characteristics of indium oxide thin film transistors

本研究探讨了利用MoO3前驱体来提高基于环保水溶液的In2O3 tft的电学性能和稳定性。具体来说,本研究考察了MoO3掺杂的In2O3 (Mo-In2O3) tft。MoO3前驱体的Mo阳离子、氢氧阴离子和氧化自由基为In2O3薄膜提供了自由电子,减少了半导体界面、半导体与绝缘体之间的陷阱位,并通过调节氧空位来提高器件的稳定性。为了验证MoO3掺杂导致的In2O3 TFT电学性质的变化,30天后的电子迁移率测量证实In2O3 TFT电子迁移率下降了80%以上,而Mo-In2O3 TFT电子迁移率保持稳定。PBS和NBS可靠性评价证实Mo- In2O3 TFT的Vth变化小于In2O3 TFT。(In2O3 TFT PBS: 5.55 V, NBS: 0.33 V, Mo-In2O3 TFT PBS: 4.04 V, NBS: 0.10 V).为了证实MoO3掺杂后In2O3膜的界面变化,利用原子力显微镜测量了表面粗糙度的差异,发现差异在4%以内。此外,通过XPS分析中氧组分的变化验证了活性层的掺杂作用。为了证明其作为有源电子器件的应用,对基于Mo-In2O3 TFT的电阻负载逆变器进行了评估,并在各种VDD条件下验证了逆变器的电压传递曲线和优异的逆变特性。[图]许宽俊等,多功能氧化钼掺杂改善氧化铟薄膜晶体管的电学特性
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引用次数: 0
Impact of Crystal Domain on Electrical Performance and Bending Durability of Flexible Organic Thin-Film Transistors with diF-TES-ADT Semiconductor 晶域对采用 diF-TES-ADT 半导体的柔性有机薄膜晶体管电气性能和弯曲耐久性的影响
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-15 DOI: 10.1007/s13391-024-00519-7
Dongwook Kim, Joel Ndikumana, Hyeonju Lee, Seullee Lee, Youngjun Yun, Jaehoon Park

In this study, we examined the impact of crystal domain on the electrical performance and durability of flexible organic thin-film transistors (OTFTs). To analyze this, we fabricated the OTFTs on a polyimide substrate using 2,8-difluoro-5,11bis(triethylsilylethynyl)anthradithiophene (diF-TES-ADT) as the organic semiconductor. To examine the influence of the film morphology and crystallinity on the electrical characteristics of OTFTs, we dissolved diF-TES-ADT in chlorobenzene and toluene solvent, annealed it at different temperatures, and then evaluated its electrical performances. The optimum annealing temperature of the diF-TES-ADT OTFTs was determined through the comprehensive analysis of the electrical parameters. The film morphology and crystallinity of organic semiconductor as a function of temperature were examined using the technical measurement analysis such as the atomic force measurement, X-ray diffraction and polarized optic microscopy. Furthermore, we demonstrated the electrical degradation of the device under prolonged bending cycles and observed the effect of bending stress on the electrical performance of OTFTs. The size of the crystalline domain and surface morphology indicated a slower deterioration of OTFT performance with an increase in the number of bending cycles. It was approved that the crystal grain size and morphology of organic semiconductor may not be critical factors determining the electrical performance of OTFTs, however, the electrical durability against bending stress was significantly degraded by these factors. We speculate that the smaller grain sizes and directionally-grown crystalline structure are highly vulnerable to bending stress, resulting in increased occurrence of void cracks and structural defects.

Graphical Abstract

在这项研究中,我们考察了晶域对柔性有机薄膜晶体管(OTFT)的电气性能和耐用性的影响。为此,我们使用 2,8-二氟-5,11-双(三乙基硅烷基)蒽(diF-TES-ADT)作为有机半导体,在聚酰亚胺基底上制作了 OTFT。为了研究薄膜形貌和结晶度对 OTFT 电学特性的影响,我们将 diF-TES-ADT 溶于氯苯和甲苯溶剂中,在不同温度下退火,然后评估其电学性能。通过对电学参数的综合分析,确定了 diF-TES-ADT OTFT 的最佳退火温度。通过原子力测量、X 射线衍射和偏振光显微镜等技术测量分析,研究了有机半导体的薄膜形貌和结晶度随温度的变化。此外,我们还证明了器件在长时间弯曲循环下的电性能衰减,并观察了弯曲应力对 OTFT 电性能的影响。结晶畴的尺寸和表面形态表明,随着弯曲次数的增加,OTFT 的性能劣化速度减慢。研究结果表明,有机半导体的晶体晶粒尺寸和形态可能不是决定 OTFT 电性能的关键因素,但这些因素会显著降低 OTFT 抗弯曲应力的电耐久性。我们推测,较小的晶粒尺寸和定向生长的晶体结构极易受到弯曲应力的影响,导致空隙裂纹和结构缺陷的发生率增加。
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引用次数: 0
All-Cobalt-Free Layered/Olivine Mixed Cathode Material for High-Electrode Density and Enhanced Cycle-Life Performance 全无钴层状/橄榄石混合阴极材料可实现高电极密度和更长的循环寿命性能
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-12 DOI: 10.1007/s13391-024-00521-z
Chang-Su Kim, Kookhan Kim, An-Seop Im, Sung-Su Kim, Jongmin Kim, Ji-Yong Eom

In this study, a high-energy-density electrode was fabricated by combining cobalt-free layered oxide (NM) with olivine LiFePO4 (LFP) nanoparticles. The resulting mixed all-cobalt-free cathode electrode effectively minimized electrode porosity by filling the interstitial spaces between the micron-sized layered-oxide particles with nanoscale LFP particles, significantly improving electrode density, and exhibiting excellent electrode conductivity. Furthermore, the composite electrode composed of NM and LFP achieved a volumetric capacity exceeding 600 mAh/cm− 3, comparable to that of typical layered oxide cathode materials, while also demonstrating enhanced cycle-life performance relative to electrodes composed solely of layered oxide or LFP. The enhanced electrochemical performance is attributed to the efficient lithium-ion and electron conduction facilitated by the intimate contact between NM and LFP particles, the suppression of NM particle degradation due to the relatively stable LFP particles on the NM surface, and the reduced particle fracture during roll-pressing. These improvements have been confirmed through electrochemical analyses and electrode observations.

Graphical Abstract

在这项研究中,通过将无钴层状氧化物(NM)与橄榄石型磷酸铁锂(LFP)纳米颗粒相结合,制造出了一种高能量密度电极。通过用纳米级 LFP 颗粒填充微米级层状氧化物颗粒之间的间隙,所得到的混合全无钴阴极电极有效地减少了电极孔隙率,显著提高了电极密度,并表现出优异的电极导电性。此外,由 NM 和 LFP 组成的复合电极的体积容量超过了 600 mAh/cm- 3,与典型的层状氧化物阴极材料相当,同时还显示出相对于仅由层状氧化物或 LFP 组成的电极更强的循环寿命性能。电化学性能的提高归功于 NM 和 LFP 颗粒之间的亲密接触促进了锂离子和电子的高效传导,NM 表面相对稳定的 LFP 颗粒抑制了 NM 颗粒的降解,以及辊压过程中颗粒断裂的减少。这些改进已通过电化学分析和电极观察得到证实。
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引用次数: 0
High-speed and Sub-ppm Detectable Tellurene NO2 Chemiresistive Room-Temperature Sensor under Humidity Environments 湿度环境下的高速、亚ppm 检测碲烯二氧化氮化学电阻室温传感器
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-11 DOI: 10.1007/s13391-024-00520-0
Yeonjin Je, Sang-Soo Chee

Two-dimensional material, tellurium, composed of tellurium, has emerged as a promising material for NO2 gas sensing due to its superior intrinsic electrical conductivity and strong affinity to NO2. However, the majority of literature on tellurene-based gas sensors has primarily focused on NO2 detection performances under dry condition, despite the importance of considering humidity-dependent detection properties for practical gas sensing applications. Here, we explore NO2 detection properties of tellurene-based chemiresistive gas sensor devices under humidity environments at room temperature. The resultant tellurene synthesized via a hydrothermal route presents 2D flake-like morphologies with highly crystalline hexagonal structures. The obtained tellurene chemiresistive sensor devices exhibit a good NO2 gas response of 35% with a fast response time of 14 s, under dry conditions. Interestingly, our tellurene-based sensor devices also present the humidity-independent NO2 gas detection performances while achieving a fast response time. These outstanding detection performances are likely due to intrinsically superior electrical conductivity and structural stability of tellurene in air.

Graphic Abstract

由碲组成的二维材料碲因其优越的内在导电性和对二氧化氮的强亲和力,已成为一种很有前途的二氧化氮气体传感材料。然而,有关碲基气体传感器的大多数文献主要关注干燥条件下的二氧化氮检测性能,尽管考虑湿度相关检测特性对于实际气体传感应用非常重要。在此,我们探讨了碲基化学电阻式气体传感器装置在室温湿度环境下的二氧化氮检测性能。通过水热法合成的碲烯呈现出二维片状形态,具有高度结晶的六边形结构。在干燥条件下,所获得的碲烯化学电阻传感器装置对 35% 的二氧化氮气体具有良好的响应,响应时间短,仅为 14 秒。有趣的是,我们的碲基传感器器件在实现快速响应时间的同时,还具有与湿度无关的二氧化氮气体检测性能。这些出色的检测性能可能是由于碲在空气中固有的优异导电性和结构稳定性。
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引用次数: 0
A Neural Network Approach for Health State Estimation of Lithium-Ion Batteries Incorporating Physics Knowledge 结合物理知识的锂离子电池健康状态估计神经网络方法
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-31 DOI: 10.1007/s13391-024-00518-8
Guoqing Sun, Yafei Liu, Xuewen Liu

The assessment of the State of Health (SOH) of lithium-ion batteries is paramount to ensuring the safety and reliability of battery management systems. Numerous researchers have employed Equivalent Circuit Models (ECM) and data-driven methodologies to estimate SOH. Each methodology has its merits and drawbacks, yet their integration poses substantial challenges. This paper proposes a novel approach for SOH estimation that synthesizes ECM with data-driven techniques. Initially, parameters for a second-order ECM are identified utilizing the voltage rebound characteristics of lithium-ion batteries. Subsequently, a predictive model is established employing a Long Short-Term Memory (LSTM) neural network. Finally, features extracted from the ECM and the dataset are utilized as inputs for the LSTM neural network to predict SOH. The efficacy of the proposed technique is corroborated by datasets from NASA and CALCE. Results indicate that the novel method’s maximum Root Mean Square Error (RMSE) is confined to 0.79%, and the Mean Absolute Error (MAE) is limited to 0.47%. Compared to other methods, this approach exhibits faster convergence, higher precision, and enhanced generalizability.

Graphical Abstract

评估锂离子电池的健康状况(SOH)对于确保电池管理系统的安全性和可靠性至关重要。许多研究人员采用等效电路模型 (ECM) 和数据驱动方法来估算 SOH。每种方法都有其优点和缺点,但它们之间的整合却带来了巨大的挑战。本文提出了一种将 ECM 与数据驱动技术相结合的 SOH 估算新方法。首先,利用锂离子电池的电压反弹特性确定二阶 ECM 的参数。随后,利用长短期记忆(LSTM)神经网络建立预测模型。最后,从 ECM 和数据集中提取的特征被用作 LSTM 神经网络的输入,以预测 SOH。来自 NASA 和 CALCE 的数据集证实了所提技术的有效性。结果表明,新方法的最大均方根误差 (RMSE) 限制在 0.79%,平均绝对误差 (MAE) 限制在 0.47%。与其他方法相比,该方法收敛速度更快、精度更高、普适性更强。
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引用次数: 0
Enhanced Magnetic Permeability Through Improved Packing Density for Thin-Film Type Power Inductors for High-Frequency Applications 通过提高高频应用薄膜型功率电感器的填料密度来增强磁导率
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-20 DOI: 10.1007/s13391-024-00517-9
Sung Yong An, Boum Seock Kim

This study investigates methods to enhance the permeability of metal magnetic composites, crucial for the performance of thin film power inductors in high-frequency applications, such as those in contemporary smartphones operating in the MHz range. Traditional reliance on ferrite magnetic materials is eschewed in favor of metal magnetic materials combined with epoxy to create novel composites aimed at optimizing packing density and significantly increasing magnetic permeability. The impact on permeability is explored using four different metal powders: pure iron (FE), Fe-Si (FS), Fe-Si-B-C-Cr (AM), and Fe-Si-B-Nb-Cu (NC). The FE sample is produced using carbonyl iron powder, resulting in a particle size (D50) of 2.1 μm. The FS sample, produced through gas atomization, has a particle size of 17.5 μm, while the AM and NC samples, produced via water atomization, yield particle sizes (D50) of 19.4 μm and 23 μm, respectively. Analyses using X-ray diffraction (XRD) and Mösbauer spectroscopy reveal that FE and FS samples have crystalline structures, whereas AM and NC are amorphous. Scanning electron microscopy confirms the spherical shape of particles in all samples. Theoretical calculations, based on Ollendorff’s theory of permeability and Suzuki and Oshima’s models on packing fraction, suggest that a composite with a ratio of 8:1.2:0.8 and particle sizes of approximately 25 μm, 1.5 μm, and 0.1 μm, respectively, could achieve a permeability value of up to 138.1. This demonstrates the potential for achieving high permeability at MHz frequencies through strategic packing of voids with submicron and nanopowders, marking a significant advancement in the field of thin film power inductors.

Graphical Abstract

本研究探讨了提高金属磁性复合材料磁导率的方法,这对薄膜功率电感器在高频应用(如在兆赫范围内工作的当代智能手机)中的性能至关重要。我们摒弃了对铁氧体磁性材料的传统依赖,转而采用金属磁性材料与环氧树脂相结合的新型复合材料,旨在优化堆积密度并显著提高磁导率。我们使用四种不同的金属粉末探讨了对磁导率的影响:纯铁(FE)、铁硅(FS)、铁硅-B-C-Cr(AM)和铁硅-B-Nb-Cu(NC)。FE 样品由羰基铁粉制成,粒度 (D50) 为 2.1 μm。通过气体雾化生产的 FS 样品的粒度为 17.5 μm,而通过水雾化生产的 AM 和 NC 样品的粒度(D50)分别为 19.4 μm 和 23 μm。利用 X 射线衍射(XRD)和莫斯鲍尔光谱进行的分析表明,FE 和 FS 样品具有晶体结构,而 AM 和 NC 则是无定形的。扫描电子显微镜证实所有样品的颗粒都呈球形。根据 Ollendorff 的渗透率理论以及 Suzuki 和 Oshima 的堆积分数模型进行的理论计算表明,比例为 8:1.2:0.8、粒径分别约为 25 μm、1.5 μm 和 0.1 μm 的复合材料的渗透率可达 138.1。这表明,通过用亚微米和纳米粉体对空隙进行策略性填料,有可能在 MHz 频率下实现高磁导率,这标志着薄膜功率电感器领域取得了重大进展。
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引用次数: 0
Flexible Strain Sensor Based on AgNWs/MXene/SEBS with High Sensitivity and Wide Strain Range 基于 AgNWs/MXene/SEBS 的柔性应变传感器具有高灵敏度和宽应变范围
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-10 DOI: 10.1007/s13391-024-00514-y
Yubo Yao, Hongfei Dai, Mengnan Ji, Ying Han, Bo Jiang, Chi Cheng, Xiaolei Song, Ying Song, Guangfeng Wu

Flexible strain sensors that combine high sensitivity and wide range are important for developing wearable electronics. In this paper, AgNWs/MXene/SEBS flexible strain sensor with high sensitivity and wide strain range was prepared using a thermoplastic elastomer (styrene-ethylene-butene-styrene) SEBS as the polymer matrix and AgNWs and MXene as the composite conductive fillers. The sensitivity of the AgNWs/MXene/SEBS sensor is significantly higher than that of the AgNWs/SEBS and MXene/SEBS sensors based on a single conductive filler. At 100% strain, the AgNWs/MXene/SEBS sensor has a sensitivity of 176.25. The sensor detects small strains of 0.5-5% as well as large strains of 5–50% with high linearity. The sensors remained stable after 200 cycles. The AgNWs/MXene/SEBS tensile sensors were subjected to array testing and finger bending recognition, and the sensors have promising applications in human motion monitoring.

Graphical Abstract

兼具高灵敏度和宽应变范围的柔性应变传感器对于开发可穿戴电子产品非常重要。本文以热塑性弹性体(苯乙烯-乙烯-丁烯-苯乙烯)SEBS 为聚合物基体,以 AgNWs 和 MXene 为复合导电填料,制备了具有高灵敏度和宽应变范围的 AgNWs/MXene/SEBS 柔性应变传感器。AgNWs/MXene/SEBS 传感器的灵敏度明显高于基于单一导电填料的 AgNWs/SEBS 和 MXene/SEBS 传感器。在应变为 100% 时,AgNWs/MXene/SEBS 传感器的灵敏度为 176.25。该传感器能检测到 0.5-5% 的小应变和 5-50% 的大应变,线性度很高。传感器在 200 次循环后仍保持稳定。对 AgNWs/MXene/SEBS 拉伸传感器进行了阵列测试和手指弯曲识别,该传感器在人体运动监测方面具有广阔的应用前景。 图文摘要
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引用次数: 0
Linear Conductance Modulation in Aluminum Doped Resistive Switching Memories for Neuromorphic Computing 用于神经形态计算的掺铝电阻开关存储器中的线性电导调制
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-09 DOI: 10.1007/s13391-024-00516-w
Young-Woong Song, Junseo Lee, Sein Lee, Wooho Ham, Jeong Hyun Yoon, Jeong-Min Park, Taehoon Sung, Jang-Yeon Kwon

With the advent of artificial intelligence (AI), automated machines could replace human labor in the near future. Nevertheless, AI implementation is currently confined to environments with huge power supplies and computing resources. Artificial neural networks are only implemented at the software level, which necessitates the continual retrieval of synaptic weights among devices. Physically constructing neural networks using emerging nonvolatile memories allows synaptic weights to be directly mapped, thereby enhancing the computational efficiency of AI. While resistive switching memory (RRAM) represents superior performances for in-memory computing, unresolved challenges persist regarding its nonideal properties. A significant challenge to the optimal performance of neural networks using RRAMs is the nonlinear conductance update. Ionic hopping of oxygen vacancy species should be thoroughly investigated and controlled for the successful implementation of RRAM-based AI acceleration. This study dopes tantalum oxide-based RRAM with aluminum, thus improving the nonlinear conductance modulation during the resistive switching process. As a result, the simulated classification accuracy of the trained network was significant improved.

Graphical Abstract

随着人工智能(AI)的出现,自动化机器在不久的将来可能会取代人类劳动。然而,人工智能的实现目前仅限于拥有巨大电力供应和计算资源的环境。人工神经网络只能在软件层面实现,这就需要在设备之间不断检索突触权重。利用新兴的非易失性存储器以物理方式构建神经网络,可以直接映射突触权重,从而提高人工智能的计算效率。虽然电阻开关存储器(RRAM)在内存计算方面性能优越,但它的非理想特性仍是未解决的难题。使用 RRAM 实现神经网络最佳性能的一个重大挑战是非线性电导更新。要成功实现基于 RRAM 的人工智能加速,就必须彻底研究和控制氧空位物种的离子跳跃。本研究在基于氧化钽的 RRAM 中掺入了铝,从而改善了电阻开关过程中的非线性电导调制。因此,训练网络的模拟分类准确性得到了显著提高。
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引用次数: 0
Hydrangea Macrophylla-Like CeO2 Coated by Nitrogen-Doped Carbon as Highly Efficient ORR Cathode Catalyst in a Hybrid Proton Battery 掺氮碳包覆的绣球花状 CeO2 作为混合质子电池中的高效 ORR 阴极催化剂
IF 2.1 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-05 DOI: 10.1007/s13391-024-00515-x
Rui Zhang, Huizhen Si, Qizhao Hu, Yangbo Cui, Shangbin Sang, Kaiyu Liu, Hongtao Liu, Qiumei Wu, Xianggong Zhang

In this paper, nitrogen-doped carbon (NC) coated tens nanometer hydrangea macrophylla-like CeO2(CeO2-NC) was synthesized by simple hydrothermal and polymeric calcination approach. Samples are characterised by SEM, Raman spectroscopy, XPS, etc. CeO2-NC shows an initial potential of 0.90V (vs. Ag/AgCl) in 9.5 M H3PO4. In addition, the CeO2-NC composite also exhibits a high limiting current (6.25 mA mg−1). CeO2-NC effectively combines the high initial potential of CeO2 with the high limiting current of NC. Moreover, a hybrid proton battery assembled with CeO2-NC composite as the cathode catalyst and MoO3 (1 mg) as anode catalyst can produce a high capacity of 261.7 mAh at 1 A g−1. The hybrid battery also exhibits excellent catalytic stability. After 1000 cycles at a high current density of 15 A g−1, the capacity of the battery still remains 125.0 mAh, with a retention rate of approximately 90.9%. The improvement in battery performance is due to the use of NC to coat CeO2, which improves the limiting current and durability of the electrode. The presented hybrid proton batteries have further enriched the application of electrochemical energy storage devices, and the preliminary exploration of cathode catalysts significantly improved the catalytic performance of ORR under acidic conditions.

Graphical Abstract

本文采用简单的水热法和聚合煅烧法合成了氮掺杂碳(NC)包覆的数十纳米绣球花状 CeO2(CeO2-NC)。样品由 SEM、拉曼光谱、XPS 等进行表征。CeO2-NC 在 9.5 M H3PO4 中的初始电位为 0.90V(相对于 Ag/AgCl)。此外,CeO2-NC 复合材料还显示出很高的极限电流(6.25 mA mg-1)。CeO2-NC 有效地结合了 CeO2 的高初始电位和 NC 的高极限电流。此外,以 CeO2-NC 复合材料为阴极催化剂、MoO3(1 毫克)为阳极催化剂组装的混合质子电池在 1 A g-1 的条件下可产生 261.7 毫安时的高容量。这种混合电池还具有出色的催化稳定性。在 15 A g-1 的高电流密度下循环 1000 次后,电池容量仍为 125.0 mAh,保持率约为 90.9%。电池性能的提高得益于使用 NC 包覆 CeO2,从而提高了电极的极限电流和耐用性。所提出的混合质子电池进一步丰富了电化学储能装置的应用,而阴极催化剂的初步探索则显著提高了酸性条件下 ORR 的催化性能。
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引用次数: 0
期刊
Electronic Materials Letters
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