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Low-temperature water electrolysis can rapidly produce environmentally sustainable or green hydrogen, and is a prospective means of storing energy from renewable but intermittent power sources, such as wind and solar, in future clean energy infrastructure (1-4). Commercial water electrolysis either use liquid alkaline electrolyte or proton exchange membrane electrolyte (1). The proton exchange membrane water electrolysis (PEMWE) offers more advantages than the alkaline counterpart, such as higher purity of H 2 , lower resistance losses, more compact design, and what the most important is the compatible with the intermittent of the renewable energy (1-2). The grant challenge remaining in PEMWE is the development of the highly active, cost effective and stable catalysts for oxygen evolution reaction (OER), which is very sluggish requiring large amounts of precious metal as the catalysts, such as Ir, Ru and their oxides (1). In PEM water electrolysis cells, the catalysts should have high surface areas and high porosities that exposit sufficient active sites available to the reactants and electrolyte, as well as transferring the bubble out of the catalyst surface to ensure a fast mass transfer (5). Also, the OER is dependent on the inherent conductivity of the catalysts or the supports (1). For example, poor electronic conductivity within the catalyst layer will result in poor lateral conductivity across the catalyst layer, thus catalyst not in the vicinity of the porous transport layer will not participate in the reaction. To enable the widespread penetration of the PEMWE technologies, it is urgently to reduce the Ir loading to the sustainable level (~ 0.3 mg/cm 2 ) compared with the current commercial usage (2-6 mg/cm 2 ). Alternatively, to develop precious metal free catalyst with high efficiency and sustained durability (5). In this presentation, we will describe a method of preparing highly active yet stable synergistic electrocatalysts for oxygen evolution reaction for PEMWE. The new catalysts contain IrCoOx/ RuCoOx cluster and La Shanghai Pujiang talent Plan, Shanghai, China; Argonne National Laboratory through Maria Goeppert Mayer Fellowship, US; State Key Laboratory of Metal Matrix Composites, shanghai Jiao Tong university, Shanghai, China. The works performed at Hydrogen research center, shanghai Jiao Tong university, and Argonne National Laboratory’s Center for Nanoscale Materials and Advanced Photo Source. Reference: K. Ayers et al., Annu. Rev. Chem. Biomol. Eng. 10, 219–239 (2019). M. Carmo, D. L. Fritz, J. Mergel, D. Stolten, Int. J. Hydrogen Energy 38, 4901–4934 (2013). M. T. M. Koper, J. Electroanal. Chem. 660, 254–260 (2011). R. D. L. Smith et al., Science 340, 60–63 (2013). Chong et al., Science 380, 609–616 (2023). Chong et al., Adv. Energy Mater. 2023, 2302306.
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Lina Chong
Wenjiang Ding
Meeting abstracts/Meeting abstracts (Electrochemical Society. CD-ROM)
Universal Alloy (United States)
RE Hydrogen (United Kingdom)
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Chong et al. (Fri,) studied this question.
www.synapsesocial.com/papers/68e5cfe5b6db643587565a9e — DOI: https://doi.org/10.1149/ma2024-01341804mtgabs