Fuel cells

    Fuel cells

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    Rational Design and Synthesis of Low-Temperature Fuel Cell Electrocatalysts
    Na Tian, Bang-An Lu, Xiao-Dong Yang, Rui Huang, Yan-Xia Jiang, Zhi-You Zhou, Shi-Gang Sun
    Electrochemical Energy Reviews    2018, 1 (1): 54-83.   DOI: 10.1007/s41918-018-0004-1
    Abstract790)      PDF       Save
    Recent progresses in proton exchange membrane fuel cell electrocatalysts are reviewed in this article in terms of cathodic and anodic reactions with a focus on rational design. These designs are based around gaining active sites using model surface studies and include high-index faceted Pt and Pt-alloy nanocrystals for anodic electrooxidation reactions as well as Pt-based alloy/core-shell structures and carbon-based non-precious metal catalysts for cathodic oxygen reduction reactions (ORR). High-index nanocrystals, alloy nanoparticles, and support efects are highlighted for anodic catalysts, and current developments in ORR electrocatalysts with novel structures and diferent compositions are emphasized for cathodic catalysts. Active site structures, catalytic performances, and stability in fuel cells are also reviewed for carbon-based non-precious metal catalysts. In addition, further developmental perspectives and the current status of advanced fuel cell electrocatalysts are provided.

    Full-text: https://link.springer.com/article/10.1007/s41918-018-0004-1
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    Core-Shell-Structured Low-Platinum Electrocatalysts for Fuel Cell Applications
    Rongfang Wang, Hui Wang, Fan Luo, Shijun Liao
    Electrochemical Energy Reviews    2018, 1 (3): 324-387.   DOI: 10.1007/s41918-018-0013-0
    Abstract772)      PDF       Save
    Pt-based catalysts are the most efcient catalysts for low-temperature fuel cells. However, commercialization is impeded by prohibitively high costs and scarcity. One of the most efective strategies to reduce Pt loading is to deposit a monolayer or a few layers of Pt over other metal cores to form core-shell-structured electrocatalysts. In core-shell-structured electrocatalysts, the compositions of the core can be divided into fve classes:single-precious metallic cores represented by Pd, Ru, and Au; singlenon-precious metallic cores represented by Cu, Ni, Co, and Fe; alloy cores containing 3d, 4d or 5d metals; and carbide and nitride cores. Of these, researchers have found that carbide and nitride cores can yield tremendous advantages over alloy cores in terms of cost and promotional activities of Pt shells. In addition, desirable shells with reasonable thicknesses and compositions have been recognized to play a dominant role in electrocatalytic performances. And recently, researchers have also found that the catalytic activity of core-shell-structured catalysts is dependent on the binding energy of the adsorbents, which is determined by the d-band center of Pt. The shifting of this d-band center in turn is mainly afected by strain and electronic efects, which can be adjusted by adjusting core compositions and shell thicknesses of catalysts. In the development of these core-shell structures, optimal synthesis methods are of primary concern because they directly determine the practical application potential of the resulting electrocatalysts. And in this article, the principles behind core-shell-structured low-Pt electrocatalysts and the developmental progresses of various synthesis methods along with the traits of each type of core and its efects on Pt shell catalytic activities are discussed. In addition, perspectives on this type of catalyst are discussed and future research directions are proposed.

    Full-text:https://link.springer.com/article/10.1007/s41918-018-0013-0
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    Metal-Nitrogen-Carbon Catalysts for Oxygen Reduction in PEM Fuel Cells: Self-Template Synthesis Approach to Enhancing Catalytic Activity and Stability
    Yanghua He, Qiang Tan, Leilei Lu, Joshua Sokolowski, Gang Wu
    Electrochemical Energy Reviews    2019, 2 (2): 231-251.   DOI: 10.1007/s41918-019-00031-9
    Abstract769)      PDF       Save
    Proton exchange membrane fuel cells (PEMFCs) are leading candidates in the utilization of clean energy resources for application in transportation, stationary, and portable devices. In PEMFCs, cathode catalysts are crucial for overall performance and durability due to kinetically slow oxygen reduction reactions (ORR). Because platinum (Pt), a state-of-the-art ORR catalyst, is rare and expensive, the development of high-performance platinum metal group (PGM)-free catalysts is highly desirable for future fuel cell technologies. Among the various PGM-free catalyst formulations, metal and nitrogen co-doped carbon (M-N-C, M:Fe, Co, or Mn) catalysts have exhibited encouraging activity and stability in acidic media for ORR and possess great potential to replace Pt in the future. Therefore, based on our extensive experience in the feld of ORR catalysis, this review will comprehensively summarize the basic principles in the design and synthesis of M-N-C catalysts for durable, inexpensive, and high-performance PEMFCs with an emphasis on Co-and Mn-N-C catalysts to avoid Fenton reactions between Fe2+ and H2O2, which can generate free radicals and lead to the degradation of catalysts, ionomers, and membranes in PEMFCs. Furthermore, template-free 3D hydrocarbon frameworks as attractive precursors to advanced M-N-C catalysts will be discussed to signifcantly enhance intrinsic ORR activities in acidic media. In addition, long-term performance durability of M-N-C cathodes will be discussed extensively to provide potential solutions to enhance catalyst stability in PEMFCs. Finally, this review will provide an overall perspective on the progress, challenges, and solutions of PGM-free catalysts for future PEMFC technologies.

    Full-text:https://link.springer.com/article/10.1007/s41918-019-00031-9/fulltext.html
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    Modeling of PEM Fuel Cell Catalyst Layers: Status and Outlook
    Pang-Chieh Sui, Xun Zhu, Ned Djilali
    Electrochemical Energy Reviews    2019, 2 (3): 428-466.   DOI: 10.1007/s41918-019-00043-5
    Abstract894)            Save

    Computational modeling has played a key role in advancing the performance and durability of polymer electrolyte membrane fuel cells (PEMFCs). In recent years there has been a signifcant focus on PEMFC catalyst layers because of their determining impact on cost and and durability. Further progress in the design of better performance, cheaper and more durable catalyst layers is required to pave the way for large scale deployment of PEMFCs. The catalyst layer poses many challenges from a modeling standpoint:it consists of a complex, multi-phase, nanostructured porous material that is difcult to characterize; and it hosts an array of coupled transport phenomena including fow of gases, liquid water, heat and charged occurring in conjunction with electrochemical reactions. This review paper examines several aspects of state-of-the-art modeling and simulation of PEMFC catalyst layers, with a view of synthesizing the theoretical foundations of various approaches, identifying gaps and outlining critical needs for further research. The review starts with a rigorous revisiting of the mathematical framework based on the volume averaging method. Various macroscopic models reported in the literature that describe the salient transport phenomena are then introduced, and their links with the volume averaged method are elucidated. Other classes of modeling and simulation methods with diferent levels of resolution of the catalyst layer structure, e.g. the pore scale model which treats materials as continuum, and various meso- and microscopic methods, which take into consideration the dynamics at the sub-grid level, are reviewed. Strategies for multiscale simulations that can bridge the gap between macroscopic and microscopic models are discussed. An important aspect pertaining to transport properties of catalyst layers is the modeling and simulation of the fabrication processes which is also reviewed. Last but not least, the review examines modeling of liquid water transport in the catalyst layer and its implications on the overall transport properties. The review concludes with an outlook on future research directions.


    Full-text:https://link.springer.com/article/10.1007/s41918-019-00043-5/fulltext.html

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