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银复合提高质子交换膜水电解槽中RuO的水电解活性和耐久性。

Silver Compositing Boosts Water Electrolysis Activity and Durability of RuO in a Proton-Exchange-Membrane Water Electrolyzer.

作者信息

Tang Jiayi, Zhong Yijun, Su Chao, Shao Zongping

机构信息

WA School of Mines: Minerals, Energy and Chemical Engineering (WASM-MECE) Curtin University Perth WA 6102 Australia.

School of Energy and Power Jiangsu University of Science and Technology Zhenjiang 212100 China.

出版信息

Small Sci. 2023 Jul 18;3(9):2300055. doi: 10.1002/smsc.202300055. eCollection 2023 Sep.

DOI:10.1002/smsc.202300055
PMID:40212966
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11936012/
Abstract

Proton-exchange-membrane water electrolyzers (PEMWEs) are of particular interest for green hydrogen production, where the oxygen evolution reaction (OER) at the anode largely determines the overall efficiency. Up to now, only ultrafine IrO catalyst gives desirable performance, while its scarcity and high cost inhibit the widespread application. RuO catalyst is the most promising alternative, while its practical application is greatly hindered by poor durability. Herein, the greatly boosted performance of conventional sub-micrometer RuO by compositing with Ag is reported, and both the morphology of Ag and the compositing way significantly affect the electrolysis performance. The PEMWE fabricated with a two-layer RuO/Ag nanowire (NWs) composite anode achieves 1.77 A cm at 2.00 V, due to a prominent 44.6 times increase of the electronic conductivity, which greatly improves the catalyst utilization. In addition, mass transportation at high-current-density region is enhanced due to the highly porous feature of Ag NW layer. Long-term stability under high current density of 1 A cm for 100 h is proved with the composite anode, due to the suppressed degradation of RuO by silver compositing. This work may accelerate the widespread commercialization of PEMWEs by providing a new way for developing IrO-free anode.

摘要

质子交换膜水电解槽(PEMWEs)在绿色制氢方面备受关注,其中阳极的析氧反应(OER)在很大程度上决定了整体效率。到目前为止,只有超细IrO催化剂具有理想的性能,但其稀缺性和高成本阻碍了其广泛应用。RuO催化剂是最有前景的替代物,但其实际应用因耐久性差而受到极大阻碍。在此,报道了通过与Ag复合显著提高传统亚微米RuO的性能,并且Ag的形态和复合方式都显著影响电解性能。采用双层RuO/Ag纳米线(NWs)复合阳极制备的PEMWE在2.00 V时实现了1.77 A cm的电流密度,这归因于电子电导率显著提高了44.6倍,极大地提高了催化剂利用率。此外,由于Ag NW层的高度多孔特性,高电流密度区域的传质得到增强。使用复合阳极证明了在1 A cm的高电流密度下100 h的长期稳定性,这是由于银复合抑制了RuO的降解。这项工作可能通过提供一种开发无IrO阳极的新方法来加速PEMWEs的广泛商业化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e79a/11936012/43c6538eb88f/SMSC-3-2300055-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e79a/11936012/c41599b2a33b/SMSC-3-2300055-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e79a/11936012/aa570f1a47f6/SMSC-3-2300055-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e79a/11936012/28cd7161062d/SMSC-3-2300055-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e79a/11936012/9ac4d4cdaf41/SMSC-3-2300055-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e79a/11936012/43c6538eb88f/SMSC-3-2300055-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e79a/11936012/c41599b2a33b/SMSC-3-2300055-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e79a/11936012/aa570f1a47f6/SMSC-3-2300055-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e79a/11936012/28cd7161062d/SMSC-3-2300055-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e79a/11936012/9ac4d4cdaf41/SMSC-3-2300055-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e79a/11936012/43c6538eb88f/SMSC-3-2300055-g004.jpg

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本文引用的文献

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Perovskite-Based Electrocatalysts for Cost-Effective Ultrahigh-Current-Density Water Splitting in Anion Exchange Membrane Electrolyzer Cell.用于阴离子交换膜电解槽中具有成本效益的超高电流密度水分解的钙钛矿基电催化剂。
Small Methods. 2022 Nov;6(11):e2201099. doi: 10.1002/smtd.202201099. Epub 2022 Oct 17.
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Modulating the Electronic Structure of RuO through Cr Solubilizing for Improved Oxygen Evolution Reaction.
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Small Methods. 2022 Sep;6(9):e2200636. doi: 10.1002/smtd.202200636. Epub 2022 Jul 25.
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Size Effects of Electrocatalysts: More Than a Variation of Surface Area.电催化剂的尺寸效应:不仅仅是表面积的变化
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Kinetics of Hydrogen Evolution Reactions in Acidic Media on Pt, Pd, and MoS.铂、钯和二硫化钼在酸性介质中析氢反应的动力学
Langmuir. 2022 Apr 12;38(14):4341-4350. doi: 10.1021/acs.langmuir.2c00090. Epub 2022 Apr 1.
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