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碱性介质中的电催化及基于碱性膜的能源技术

Electrocatalysis in Alkaline Media and Alkaline Membrane-Based Energy Technologies.

作者信息

Yang Yao, Peltier Cheyenne R, Zeng Rui, Schimmenti Roberto, Li Qihao, Huang Xin, Yan Zhifei, Potsi Georgia, Selhorst Ryan, Lu Xinyao, Xu Weixuan, Tader Mariel, Soudackov Alexander V, Zhang Hanguang, Krumov Mihail, Murray Ellen, Xu Pengtao, Hitt Jeremy, Xu Linxi, Ko Hsin-Yu, Ernst Brian G, Bundschu Colin, Luo Aileen, Markovich Danielle, Hu Meixue, He Cheng, Wang Hongsen, Fang Jiye, DiStasio Robert A, Kourkoutis Lena F, Singer Andrej, Noonan Kevin J T, Xiao Li, Zhuang Lin, Pivovar Bryan S, Zelenay Piotr, Herrero Enrique, Feliu Juan M, Suntivich Jin, Giannelis Emmanuel P, Hammes-Schiffer Sharon, Arias Tomás, Mavrikakis Manos, Mallouk Thomas E, Brock Joel D, Muller David A, DiSalvo Francis J, Coates Geoffrey W, Abruña Héctor D

机构信息

Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, United States.

Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States.

出版信息

Chem Rev. 2022 Mar 23;122(6):6117-6321. doi: 10.1021/acs.chemrev.1c00331. Epub 2022 Feb 8.

Abstract

Hydrogen energy-based electrochemical energy conversion technologies offer the promise of enabling a transition of the global energy landscape from fossil fuels to renewable energy. Here, we present a comprehensive review of the fundamentals of electrocatalysis in alkaline media and applications in alkaline-based energy technologies, particularly alkaline fuel cells and water electrolyzers. Anion exchange (alkaline) membrane fuel cells (AEMFCs) enable the use of nonprecious electrocatalysts for the sluggish oxygen reduction reaction (ORR), relative to proton exchange membrane fuel cells (PEMFCs), which require Pt-based electrocatalysts. However, the hydrogen oxidation reaction (HOR) kinetics is significantly slower in alkaline media than in acidic media. Understanding these phenomena requires applying theoretical and experimental methods to unravel molecular-level thermodynamics and kinetics of hydrogen and oxygen electrocatalysis and, particularly, the proton-coupled electron transfer (PCET) process that takes place in a proton-deficient alkaline media. Extensive electrochemical and spectroscopic studies, on single-crystal Pt and metal oxides, have contributed to the development of activity descriptors, as well as the identification of the nature of active sites, and the rate-determining steps of the HOR and ORR. Among these, the structure and reactivity of interfacial water serve as key potential and pH-dependent kinetic factors that are helping elucidate the origins of the HOR and ORR activity differences in acids and bases. Additionally, deliberately modulating and controlling catalyst-support interactions have provided valuable insights for enhancing catalyst accessibility and durability during operation. The design and synthesis of highly conductive and durable alkaline membranes/ionomers have enabled AEMFCs to reach initial performance metrics equal to or higher than those of PEMFCs. We emphasize the importance of using membrane electrode assemblies (MEAs) to integrate the often separately pursued/optimized electrocatalyst/support and membranes/ionomer components. methods, at multiscales, and simulations provide a mechanistic understanding of electron, ion, and mass transport at catalyst/ionomer/membrane interfaces and the necessary guidance to achieve fuel cell operation in air over thousands of hours. We hope that this Review will serve as a roadmap for advancing the scientific understanding of the fundamental factors governing electrochemical energy conversion in alkaline media with the ultimate goal of achieving ultralow Pt or precious-metal-free high-performance and durable alkaline fuel cells and related technologies.

摘要

基于氢能的电化学能量转换技术有望推动全球能源格局从化石燃料向可再生能源转变。在此,我们全面综述了碱性介质中的电催化基础及其在碱性能源技术中的应用,特别是碱性燃料电池和水电解槽。相对于需要基于铂的电催化剂的质子交换膜燃料电池(PEMFC),阴离子交换(碱性)膜燃料电池(AEMFC)能够使用非贵金属电催化剂来催化缓慢的氧还原反应(ORR)。然而,碱性介质中的氢氧化反应(HOR)动力学明显比酸性介质中慢。理解这些现象需要应用理论和实验方法来揭示氢和氧电催化的分子水平热力学和动力学,特别是在缺质子碱性介质中发生的质子耦合电子转移(PCET)过程。对单晶铂和金属氧化物进行的广泛电化学和光谱研究有助于开发活性描述符,以及确定活性位点的性质和HOR与ORR的速率决定步骤。其中,界面水的结构和反应性是关键的电位和pH依赖动力学因素,有助于阐明酸和碱中HOR和ORR活性差异的根源。此外,有意调节和控制催化剂-载体相互作用为提高运行过程中催化剂的可及性和耐久性提供了有价值的见解。高导电性和耐用性碱性膜/离聚物的设计与合成使AEMFC能够达到与PEMFC相当或更高的初始性能指标。我们强调使用膜电极组件(MEA)来整合通常分别研究/优化的电催化剂/载体和膜/离聚物组件的重要性。多尺度的实验方法和模拟提供了对催化剂/离聚物/膜界面处电子、离子和质量传输机制的理解,并为实现燃料电池在空气中数千小时的运行提供了必要的指导。我们希望这篇综述将成为推进对碱性介质中电化学能量转换基本因素科学理解的路线图,最终目标是实现超低铂或无贵金属的高性能、耐用碱性燃料电池及相关技术。

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