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    Recent Progress in MXene-Based Materials for Metal-Sulfur and Metal-Air Batteries: Potential High-Performance Electrodes
    Anmin Liu, Xingyou Liang, Xuefeng Ren, Weixin Guan, Tingli Ma
    Electrochemical Energy Reviews    2022, 5 (1): 112-144.   DOI: 10.1007/s41918-021-00110-w
    Abstract9934)      PDF       Save
    MXene|Metal-sulfur batteries|Metal-air batteries|Electrode
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    Self-Supported Graphene Nanosheet-Based Composites as Binder-Free Electrodes for Advanced Electrochemical Energy Conversion and Storage
    Bowen Ren, Hao Cui, Chengxin Wang
    Electrochemical Energy Reviews    2022, 5 (S2): 32-.   DOI: 10.1007/s41918-022-00138-6
    Abstract781)      PDF       Save
    Graphene is composed of single-layered sp2 graphite and has been widely used in electrochemical energy conversion and storage due to its appealing physical and chemical properties. In recent years, a new kind of the self-supported graphene nanosheet-based composite (GNBC) has attracted significant attention. Compared with conventional powdered materials, a binder-free electrode architecture has several strengths, including a large surface area, enhanced reaction kinetics, and great structural stability, and these strengths allow users to realize the full potential of graphene. Based on these findings, this review presents preparation strategies and properties of self-supported GNBCs. Additionally, it highlights recent significant developments with integrated binder-free electrodes for several practical applications, such as lithium-ion batteries, lithium-metal batteries, supercapacitors, water splitting and metal-air batteries. In addition, the remaining challenges and future perspectives in this emerging field are also discussed.
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    Lead-Carbon Batteries toward Future Energy Storage: From Mechanism and Materials to Applications
    Jian Yin, Haibo Lin, Jun Shi, Zheqi Lin, Jinpeng Bao, Yue Wang, Xuliang Lin, Yanlin Qin, Xueqing Qiu, Wenli Zhang
    Electrochemical Energy Reviews    2022, 5 (3): 2-.   DOI: 10.1007/s41918-022-00134-w
    Abstract2392)      PDF       Save
    The lead acid battery has been a dominant device in large-scale energy storage systems since its invention in 1859. It has been the most successful commercialized aqueous electrochemical energy storage system ever since. In addition, this type of battery has witnessed the emergence and development of modern electricity-powered society. Nevertheless, lead acid batteries have technologically evolved since their invention. Over the past two decades, engineers and scientists have been exploring the applications of lead acid batteries in emerging devices such as hybrid electric vehicles and renewable energy storage; these applications necessitate operation under partial state of charge. Considerable endeavors have been devoted to the development of advanced carbon-enhanced lead acid battery (i.e., lead-carbon battery) technologies. Achievements have been made in developing advanced lead-carbon negative electrodes. Additionally, there has been significant progress in developing commercially available lead-carbon battery products. Therefore, exploring a durable, long-life, corrosion-resistive lead dioxide positive electrode is of significance. In this review, the possible design strategies for advanced maintenance-free lead-carbon batteries and new rechargeable battery configurations based on lead acid battery technology are critically reviewed. Moreover, a synopsis of the lead-carbon battery is provided from the mechanism, additive manufacturing, electrode fabrication, and full cell evaluation to practical applications.
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    Photochemical Systems for Solar-to-Fuel Production
    Ya Liu, Feng Wang, Zihao Jiao, Shengjie Bai, Haoran Qiu, Liejin Guo
    Electrochemical Energy Reviews    2022, 5 (3): 5-.   DOI: 10.1007/s41918-022-00132-y
    Abstract1876)      PDF       Save
    The photochemical system, which utilizes only solar energy and H2O/CO2 to produce hydrogen/carbon-based fuels, is considered a promising approach to reduce CO2 emissions and achieve the goal of carbon neutrality. To date, numerous photochemical systems have been developed to obtain a viable solar-to-fuel production system with sufficient energy efficiency. However, more effort is still needed to meet the requirements of industrial implementation. In this review, we systematically discuss a typical photochemical system for solar-to-fuel production, from classical theories and fundamental mechanisms to raw material selection, reaction condition optimization, and unit device/system advancement, from the viewpoint of ordered energy conversion. State-of-the-art photochemical systems, including photocatalytic, photovoltaic-electrochemical, photoelectrochemical, solar thermochemical, and other emerging systems, are summarized. We highlight the existing bottlenecks and discuss the developing trend of this technology. Finally, optimization strategies and new opportunities are proposed to enhance photochemical systems with higher energy efficiency.
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    Rational Design of Atomic Site Catalysts for Electrocatalytic Nitrogen Reduction Reaction: One Step Closer to Optimum Activity and Selectivity
    Yiran Ying, Ke Fan, Jinli Qiao, Haitao Huang
    Electrochemical Energy Reviews    2022, 5 (3): 6-.   DOI: 10.1007/s41918-022-00164-4
    Abstract2166)      PDF       Save
    The electrocatalytic nitrogen reduction reaction (NRR) has been one of the most intriguing catalytic reactions in recent years, providing an energy-saving and environmentally friendly alternative to the conventional Haber-Bosch process for ammonia production. However, the activity and selectivity issues originating from the activation barrier of the NRR intermediates and the competing hydrogen evolution reaction result in the unsatisfactory NH3 yield rate and Faradaic efficiency of current NRR catalysts. Atomic site catalysts (ASCs), an emerging group of heterogeneous catalysts with a high atomic utilization rate, selectivity, and stability, may provide a solution. This article undertakes an exploration and systematic review of a highly significant research area:the principles of designing ASCs for the NRR. Both the theoretical and experimental progress and state-of-the-art techniques in the rational design of ASCs for the NRR are summarized, and the topic is extended to double-atom catalysts and boron-based metal-free ASCs. This review provides guidelines for the rational design of ASCs for the optimum activity and selectivity for the electrocatalytic NRR.
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    Copper-Based Catalysts for Electrochemical Carbon Dioxide Reduction to Multicarbon Products
    Fangfang Chang, Meiling Xiao, Ruifang Miao, Yongpeng Liu, Mengyun Ren, Zhichao Jia, Dandan Han, Yang Yuan, Zhengyu Bai, Lin Yang
    Electrochemical Energy Reviews    2022, 5 (3): 4-.   DOI: 10.1007/s41918-022-00139-5
    Abstract1832)      PDF       Save
    Electrochemical conversion of carbon dioxide into fuel and chemicals with added value represents an appealing approach to reduce the greenhouse effect and realize a carbon-neutral cycle, which has great potential in mitigating global warming and effectively storing renewable energy. The electrochemical CO2 reduction reaction (CO2RR) usually involves multiproton coupling and multielectron transfer in aqueous electrolytes to form multicarbon products (C2+ products), but it competes with the hydrogen evolution reaction (HER), which results in intrinsically sluggish kinetics and a complex reaction mechanism and places higher requirements on the design of catalysts. In this review, the advantages of electrochemical CO2 reduction are briefly introduced, and then, different categories of Cu-based catalysts, including monometallic Cu catalysts, bimetallic catalysts, metal-organic frameworks (MOFs) along with MOF-derived catalysts and other catalysts, are summarized in terms of their synthesis method and conversion of CO2 to C2+ products in aqueous solution. The catalytic mechanisms of these catalysts are subsequently discussed for rational design of more efficient catalysts. In response to the mechanisms, several material strategies to enhance the catalytic behaviors are proposed, including surface facet engineering, interface engineering, utilization of strong metal-support interactions and surface modification. Based on the above strategies, challenges and prospects are proposed for the future development of CO2RR catalysts for industrial applications.
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    Recent Progresses in Oxygen Reduction Reaction Electrocatalysts for Electrochemical Energy Applications
    Yahao Li, Qingyu Li, Hongqiang Wang, Lei Zhang, David P. Wilkinson, Jiujun Zhang
    Electrochemical Energy Reviews    2019, 2 (4): 518-538.   DOI: 10.1007/s41918-019-00052-4
    Abstract16532)      PDF       Save

    Electrochemical energy storage systems such as fuel cells and metal-air batteries can be used as clean power sources for electric vehicles. In these systems, one necessary reaction at the cathode is the catalysis of oxygen reduction reaction (ORR), which is the rate-determining factor afecting overall system performance. Therefore, to increase the rate of ORR for enhanced system performances, efcient electrocatalysts are essential. And although ORR electrocatalysts have been intensively explored and developed, signifcant breakthroughs have yet been achieved in terms of catalytic activity, stability, cost and associated electrochemical system performance. Based on this, this review will comprehensively present the recent progresses of ORR electrocatalysts, including precious metal catalysts, non-precious metal catalysts, single-atom catalysts and metal-free catalysts. In addition, major technical challenges are analyzed and possible future research directions to overcome these challenges are proposed to facilitate further research and development toward practical application.


    Full-text:https://link.springer.com/article/10.1007/s41918-019-00052-4

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    Polybenzimidazole-Based High-Temperature Polymer Electrolyte Membrane Fuel Cells: New Insights and Recent Progress
    David Aili, Dirk Henkensmeier, Santiago Martin, Bhupendra Singh, Yang Hu, Jens Oluf Jensen, Lars N. Cleemann, Qingfeng Li
    Electrochemical Energy Reviews    2020, 3 (4): 793-845.   DOI: 10.1007/s41918-020-00080-5
    Abstract16458)      PDF       Save

    High-temperature proton exchange membrane fuel cells based on phosphoric acid-doped polybenzimidazole membranes are a technology characterized by simplified construction and operation along with possible integration with, e.g., methanol reformers. Significant progress has been achieved in terms of key materials, components and systems. This review is devoted to updating new insights into the fundamental understanding and technological deployment of this technology. Polymers are synthetically modified with basic functionalities, and membranes are improved through cross-linking and inorganic-organic hybridization. New insights into phosphoric acid along with its interactions with basic polymers, metal catalysts and carbon-based supports are recapped. Recognition of parasitic acid migration raises acid retention issues at high current densities. Acid loss via evaporation is estimated with respect to the acid inventory of membrane electrode assembly. Acid adsorption on platinum surfaces can be alleviated for platinum alloys and non-precious metal catalysts. Binders have been considered a key to the establishment of the triple-phase boundary, while recent development of binderless electrodes opens new avenues toward low Pt loadings. Often ignored microporous layers and water impacts are also discussed. Of special concern are durability issues including acid loss, platinum sintering and carbon corrosion, the latter being critical during start/stop cycling with mitigation measures proposed. Long-term durability has been demonstrated with a voltage degradation rate of less than 1 μV h-1 under steady-state tests at 160℃, while challenges remain at higher temperatures, current densities or reactant stoichiometries, particularly during dynamic operation with thermal, load or start/stop cycling.


    Full-text:https://link.springer.com/article/10.1007/s41918-020-00080-5

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    Solid-State Electrolytes for Lithium-Ion Batteries: Fundamentals, Challenges and Perspectives
    Wenjia Zhao, Jin Yi, Ping He, Haoshen Zhou
    Electrochemical Energy Reviews    2019, 2 (4): 574-605.   DOI: 10.1007/s41918-019-00048-0
    Abstract655)      PDF       Save

    With the rapid popularization and development of lithium-ion batteries, associated safety issues caused by the use of fammable organic electrolytes have drawn increasing attention. To address this, solid-state electrolytes have become the focus of research for both scientifc and industrial communities due to high safety and energy density. Despite these promising prospects, however, solid-state electrolytes face several formidable obstacles that hinder commercialization, including insuffcient lithium-ion conduction and surge transfer impedance at the interface between solid-state electrolytes and electrodes. Based on this, this review will provide an introduction into typical lithium-ion conductors involving inorganic, organic and inorganic-organic hybrid electrolytes as well as the mechanisms of lithium-ion conduction and corresponding factors afecting performance. Furthermore, this review will comprehensively discuss emerging and advanced characterization techniques and propose underlying strategies to enhance ionic conduction along with future development trends.


    Full-text:https://link.springer.com/article/10.1007/s41918-019-00048-0

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    The Electrochemical Tuning of Transition Metal-Based Materials for Electrocatalysis
    Fangming Liu, Le Zhang, Lei Wang, Fangyi Cheng
    Electrochemical Energy Reviews    2021, 4 (1): 146-168.   DOI: 10.1007/s41918-020-00089-w
    Abstract1890)      PDF       Save

    The development of clean and sustainable energy depends largely on electrocatalysis-driven technologies. Because of this, tremendous efforts have been devoted to the search for efficient electrocatalysts to reduce the overpotential and increase the selectivity of electrochemical reactions. Of the various approaches, electrochemical tuning is seen as a promising technique to controllably tune the properties of catalytic materials under mild conditions. Based on this, this review will present representative electrochemical tuning methodologies involving insertion and conversion reactions in batteries as well as in situ electrode modulation during electrocatalysis processes. This review will first provide an introduction of electrochemical tuning strategies from the perspective of reactions and devices. Subsequently, this review will present comprehensive discussions on recent advancements in the modulation of various electrocatalyst properties, including electronic structure, crystalline phase, lattice strain and dimensional size, all of which significantly impact corresponding intrinsic activity and active site exposure. This review will also highlight the merits, challenges and issues of electrochemical tuning and propose promising directions in the exploration of corresponding methods in the design and enhancement of electrocatalysts for future energy applications.


    Full-text:https://link.springer.com/article/10.1007/s41918-020-00089-w

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    MOF/PCP-based Electrocatalysts for the Oxygen Reduction Reaction
    Liang Tang, Qinshang Xu, Yu Zhang, Wenqian Chen, Minghong Wu
    Electrochemical Energy Reviews    2022, 5 (1): 32-81.   DOI: 10.1007/s41918-021-00113-7
    Abstract2353)      PDF       Save
    Electrocatalysis|Oxygen reduction reaction|Metal-organic framework|Active sites|Dimension
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    The Controllable Design of Catalyst Inks to Enhance PEMFC Performance: A Review
    Yuqing Guo, Fengwen Pan, Wenmiao Chen, Zhiqiang Ding, Daijun Yang, Bing Li, Pingwen Ming, Cunman Zhang
    Electrochemical Energy Reviews    2021, 4 (1): 67-100.   DOI: 10.1007/s41918-020-00083-2
    Abstract2238)      PDF       Save

    Typical catalyst inks in proton exchange membrane fuel cells (PEMFCs) are composed of a catalyst, its support, an ionomer and a solvent and are used with solution processing approaches to manufacture conventional catalyst layers (CLs). Because of this, catalyst ink formulation and deposition processes are closely related to CL structure and performance. However, catalyst inks with ideal rheology and optimized electrochemical performances remain lacking in the large-scale application of PEMFCs. To address this, this review will summarize current progress in the formulation, characterization, modeling and deposition of catalyst inks. In addition, this review will highlight recent advancements in catalyst ink materials and discuss corresponding complex interactions. This review will also present various catalyst ink dispersion methods with insights into their stability and introduce the application of small-angle scattering and cryogenic transmission electron microscopy (cryo-TEM) technologies in the characterization of catalyst ink microstructures. Finally, recent studies in the kinetic modeling and deposition of catalyst inks will be analyzed.


    Full-text:https://link.springer.com/article/10.1007/s41918-020-00083-2

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    Air Stability of Solid-State Sulfide Batteries and Electrolytes
    Pushun Lu, Dengxu Wu, Liquan Chen, Hong Li, Fan Wu
    Electrochemical Energy Reviews    2022, 5 (3): 3-.   DOI: 10.1007/s41918-022-00149-3
    Abstract1953)      PDF       Save
    Sulfides have been widely acknowledged as one of the most promising solid electrolytes (SEs) for all-solid-state batteries (ASSBs) due to their superior ionic conductivity and favourable mechanical properties. However, the extremely poor air stability of sulfide SEs leads to destroyed structure/performance and release of toxic H2S gas, which greatly limits mass-production/practical application of sulfide SEs and ASSBs. This review is designed to serve as an all-inclusive handbook for studying this critical issue. First, the research history and milestone breakthroughs of this field are reviewed, and this is followed by an in-depth elaboration of the theoretical paradigms that have been developed thus far, including the random network theory of glasses, hard and soft acids and bases (HSAB) theory, thermodynamic analysis and kinetics of interfacial reactions. Moreover, the characterization of air stability is reviewed from the perspectives of H2S generation, morphology evolution, mass change, component/structure variations and electrochemical performance. Furthermore, effective strategies for improving the air stabilities of sulfide SEs are highlighted, including H2S absorbents, elemental substitution, design of new materials, surface engineering and sulfide-polymer composite electrolytes. Finally, future research directions are proposed for benign development of air stability for sulfide SEs and ASSBs.
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    Effects of Crystallinity and Defects of Layered Carbon Materials on Potassium Storage: A Review and Prediction
    Xiaoxu Liu, Tianyi Ji, Hai Guo, Hui Wang, Junqi Li, Hui Liu, Zexiang Shen
    Electrochemical Energy Reviews    2022, 5 (2): 401-433.   DOI: 10.1007/s41918-021-00114-6
    Abstract3172)      PDF       Save
    Layered carbon materials (LCMs) are composed of basic carbon layer units, such as graphite, soft carbon, hard carbon, and graphene. While they have been widely applied in the anode of potassium-ion batteries, the potassium storage mechanisms and performances of various LCMs are isolated and difficult to relate to each other. More importantly, there is a lack of a systematic understanding of the correlation between the basic microstructural unit (crystallinity and defects) and the potassium storage behavior. In this review, we explored the key structural factors affecting the potassium storage in LCMs, namely, the crystallinity and defects of carbon layers, and the key parameters (La, Lc, d002, ID/IG) that characterize the crystallinity and defects of different carbon materials were extracted from various databases and literature sources. A structure-property database of LCMs was thus built, and the effects of these key structural parameters on the potassium storage properties, including the capacity, the rate and the working voltage plateau, were systematically analyzed. Based on the structure-property database analysis and the guidance of thermodynamics and kinetics, a relationship between various LCMs and potassium storage properties was established. Finally, with the help of machine learning, the key structural parameters of layered carbon anodes were used for the first time to predict the potassium storage performance so that the large amount of research data in the database could more effectively guide the scientific research and engineering application of LCMs in the future.
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    Graphene for Energy Storage and Conversion: Synthesis and Interdisciplinary Applications
    Liqi Bai, Yihe Zhang, Wangshu Tong, Li Sun, Hongwei Huang, Qi An, Na Tian, Paul K. Chu
    Electrochemical Energy Reviews    2020, 3 (2): 395-430.   DOI: 10.1007/s41918-019-00042-6
    Abstract1692)      PDF       Save

    2D graphene materials possess excellent electrical conductivity and an sp2 carbon atom structure and can be applied in light and electric energy storage and conversion applications. However, traditional methods of graphene preparation cannot keep pace with real-time synthesis, and therefore, novel graphene synthesis approaches have attracted increasing attention from researchers to accurately control graphene structure and morphology. Based on this, this review will discuss the novel synthesis of graphene for interdisciplinary applications of energy storage and conversion, which is a promising direction in the research for novel applications in photoelectrochemical cells, photo-assisted batteries, piezoelectric nanogenerators, photothermal and photomechanical devices, etc.


    Full-text:https://link.springer.com/article/10.1007/s41918-019-00042-6

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    Tailoring MXene-Based Materials for Sodium-Ion Storage: Synthesis, Mechanisms, and Applications
    Yao-Jie Lei, Zi-Chao Yan, Wei-Hong Lai, Shu-Lei Chou, Yun-Xiao Wang, Hua-Kun Liu, Shi-Xue Dou
    Electrochemical Energy Reviews    2020, 3 (4): 766-792.   DOI: 10.1007/s41918-020-00079-y
    Abstract10702)      PDF       Save

    Advanced electrodes with excellent rate performance and cycling stability are in demand for the fast development of sodium storage. Two-dimensional (2D) materials have emerged as one of the most investigated subcategories of sodium storage related anodes due to their superior electron transfer capability, mechanical flexibility, and large specific surface areas. Recently, 2D metal carbides and nitrides (MXenes), one type of the new 2D materials, are known to have competitive advantages in terms of high electroconductivity, terminal functional groups, large specific surface areas, tunable interlayer spacing, and remarkable safety. These advances endow MXenes and MXene-based materials with superior electrochemical performance when they are used as electrodes for sodium-ion storage. MXenes, however, share similar defects with other 2D materials, such as serious restacking and aggregation, which need to be improved in consideration of their further applications. In this review, we present the big family of MXenes and their synthetic methods. Furthermore, recent research reports related to progress on MXene-based materials for sodium storage are compiled, including materials design and reaction mechanisms in sodium-ion batteries and sodium metal batteries. Significantly, we discuss the challenges for existing MXene-based structures with respect to their future use as electrodes, such as low capacitance, aggregation, untenable termination groups, and unclear mechanisms, thereby providing guidance for future research on MXene-based materials for sodium-ion storage.


    Full-text:https://link.springer.com/article/10.1007/s41918-020-00079-y

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    Design Principle, Optimization Strategies, and Future Perspectives of Anode-Free Configurations for High-Energy Rechargeable Metal Batteries
    Wentao Yao, Peichao Zou, Min Wang, Houchao Zhan, Feiyu Kang, Cheng Yang
    Electrochemical Energy Reviews    2021, 4 (3): 601-631.   DOI: 10.1007/s41918-021-00106-6
    Abstract537)      PDF       Save
    Metal anodes (e.g., lithium, sodium and zinc metal anodes) based on a unique plating/stripping mechanism have been well recognized as the most promising anodes for next-generation high-energy metal batteries owing to their superior theoretical specific capacities and low redox potentials. However, realizing full utilization and the theoretical capacity of metal anodes remains challenging because of their high reactivity, poor reversibility, and nonplanar metal evolution patterns, which lead to irreversible loss of active metals and the electrolyte. To minimize the above issues, excess metal sources and flooded electrolytes are generally used for laboratory-based studies. Despite the superior cycling performance achieved for these cells, the metal-anode-excess design deviates from practical applications due to the low anode utilization, highly inflated coulombic efficiency, and undesirable volumetric capacity. In contrast, anode-free configurations can overcome these drawbacks while reducing fabrication costs and improving cell safety. In this review, the significance of anode-free configurations is elaborated, and different types of anode-free cells are introduced, including reported designs and proposed feasible yet unexplored concepts. The optimization strategies for anode-free lithium, sodium, zinc, and aluminum metal batteries are summarized. Most importantly, the remaining challenges for extending the cycle life of anode-free cells are discussed, and the requirements for anode-free cells to reach practical applications are highlighted. This comprehensive review is expected to draw more attention to anode-free configurations and bring new inspiration to the design of high-energy metal batteries.Anode-free metal batteries can deliver higher energy densities than traditional anode-excess metal batteries and metal-ion batteries. Yet the cycle life of anode-free cells is limited by the non-planar growth and low coulombic efficiency of the metal anodes. In this review, we not only systematically elaborate the working/failure mechanisms and achieved progress for the reported anode-free Li/Na/Zn/Al battery systems, but also propose a series of conceptually-feasible yet unexplored anode-free systems.
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    High-Mass-Loading Electrodes for Advanced Secondary Batteries and Supercapacitors
    Feng Wu, Mingquan Liu, Ying Li, Xin Feng, Kun Zhang, Ying Bai, Xinran Wang, Chuan Wu
    Electrochemical Energy Reviews    2021, 4 (2): 382-446.   DOI: 10.1007/s41918-020-00093-0
    Abstract659)      PDF       Save
    The growing demand for advanced electrochemical energy storage systems (EESSs) with high energy densities for electric vehicles and portable electronics is driving the electrode revolution, in which the development of high-mass-loading electrodes (HMLEs) is a promising route to improve the energy density of batteries packed in limited spaces through the optimal enlargement of active material loading ratios and reduction of inactive component ratios in overall cell devices. However, HMLEs face significant challenges including inferior charge kinetics, poor electrode structural stability, and complex and expensive production processes. Based on this, this review will provide a comprehensive summary of HMLEs, beginning with a basic presentation of factors influencing HMLE electrochemical properties, the understanding of which can guide optimal HMLE designs. Rational strategies to improve the electrochemical performance of HMLEs accompanied by corresponding advantages and bottlenecks are subsequently discussed in terms of various factors ranging from inactive component modification to active material design to structural engineering at the electrode scale. This review will also present the recent progress and approaches of HMLEs applied in various EESSs, including advanced secondary batteries (lithium-/sodium-/potassium-/aluminum-/calcium-ion batteries, lithium metal anodes, lithium-sulfur batteries, lithium-air batteries, zinc batteries, magnesium batteries) and supercapacitors. Finally, this review will examine the challenges and prospects of HMLE commercialization with a focus on thermal safety, performance evaluation, advanced characterization, and production cost assessment to guide future development.

    Full-text: https://link.springer.com/article/10.1007/s41918-020-00093-0
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    Non-noble Metal Electrocatalysts for the Hydrogen Evolution Reaction in Water Electrolysis
    Huimin Wu, Chuanqi Feng, Lei Zhang, Jiujun Zhang, David P. Wilkinson
    Electrochemical Energy Reviews    2021, 4 (3): 473-507.   DOI: 10.1007/s41918-020-00086-z
    Abstract490)      PDF       Save
    Water electrolysis is a sustainable approach for hydrogen production by using electricity from clean energy sources. However, both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER) associated with water electrolysis are kinetically sluggish, leading to low efficiency in corresponding electrolysis devices. In addition, current electrocatalysts that can catalyze both HER and OER to practical rates require noble metals such as platinum that are low in abundance and high in price, severely limiting commercialization. As a result, the development of high-performance and cost-effective non-noble metal electrocatalysts to replace noble ones has intensified. Based on this, this review will comprehensively present recent research in the design, synthesis, characterization and performance validation/optimization of non-noble metal HER electrocatalysts and analyze corresponding catalytic mechanisms. Moreover, several important types of non-noble metal electrocatalysts including zero-dimensional, one-dimensional, two-dimensional and three-dimensional materials are presented with an emphasis on morphology/structure, synergetic interaction between metal and support, catalytic property and HER activity/stability. Furthermore, existing technical challenges are summarized and corresponding research directions are proposed toward practical application.Water electrolysis is a sustainable approach for hydrogen production by using electricity from clean energy sources. However, both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) are kinetically sluggish, causing low efficiency of the electrolysis devices. The currently used noble metals, such as Pt-based electrocatalysts for catalyzing both HER and OER to practical rates, have low abundances and high price, limiting their commercialization. In this regard, developing high-performance and cost-effective non-noble metal electrocatalysts to replace noble ones has become a hot research topic.
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    High-Temperature Electrochemical Devices Based on Dense Ceramic Membranes for CO2 Conversion and Utilization
    Wenping Li, Jing-Li Luo
    Electrochemical Energy Reviews    2021, 4 (3): 518-544.   DOI: 10.1007/s41918-021-00099-2
    Abstract561)      PDF       Save
    The adverse effects of global warming and climate change have driven the exploration of feasible routes for CO2 capture, storage, conversion and utilization. The processes related to CO2 conversion in high-temperature electrochemical devices (HTEDs) using dense ceramic membranes are particularly appealing due to the simultaneous realization of highly efficient CO2 conversion and value-added chemical production as well as the generation of electricity and storage of renewable energy in some cases. Currently, most studies are focused on the two processes, CO2 electrolysis and H2O/CO2 co-electrolysis in oxygen-conducting solid oxide electrolysis cell (O-SOEC) reactors. Less attention has been paid to other meaningful CO2-conversion-related processes in HTEDs and systematic summary and analysis are currently not available. This review will fill the gap and classify the CO2-conversion-related processes in HTEDs reported in recent years into four types according to the related reactions, including assisted CO2 reduction to CO, H2O and CO2 co-conversion, dry reforming of methane and CO2 hydrogenation. Firstly, an overview of the fundamentals of HTED processes is presented, and then the related mechanism and research progress of each type of reactions in different HTEDs are elucidated and concluded accordingly. The remaining major technical issues are also briefly introduced. Lastly, the main challenges and feasible solutions as well as the future prospects of HTEDs for CO2-conversion-related processes are also discussed in this review.
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