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用于质子交换膜电解槽中酸性水氧化的钌单原子调制质子化氧化铱

Ruthenium Single-Atom Modulated Protonated Iridium Oxide for Acidic Water Oxidation in Proton Exchange Membrane Electrolysers.

作者信息

Tang Jialin, Liu Xinyan, Xiong Xiaoxia, Zeng Qisheng, Ji Yuan, Liu Chunxiao, Li Jiawei, Zeng Hongliang, Dai Yizhou, Zhang Xinyan, Li Chengbo, Peng Hongjie, Jiang Qiu, Zheng Tingting, Pao Chih-Wen, Xia Chuan

机构信息

School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu, Sichuan, 611731, P. R. China.

Key Laboratory of Quantum Physics and Photonic Quantum Information, Ministry of Education, University of Electronic Science and Technology of China, Chengdu, 611731, P. R. China.

出版信息

Adv Mater. 2024 Oct;36(41):e2407394. doi: 10.1002/adma.202407394. Epub 2024 Aug 15.

Abstract

Proton exchange membrane water electrolysers promise to usher in a new era of clean energy, but they remain a formidable obstacle in designing active and durable electrocatalysts for the acidic oxygen evolution reaction (OER). In this study, a protonated iridium oxide embedded with single-atom dispersed ruthenium atoms (HIr RuO) that demonstrates exceptional activity and stability in acidic water oxidation is introduced. The single Ru dopants favorably induce localized oxygen vacancies in the Ir─O lattice, synergistically strengthening the adsorption of OOH* intermediates and enhancing the intrinsic OER activity. In addition, the preferential oxidation of Ru and the electronegativity of the oxygen vacancies significantly stabilize the Ir─O active sites, improving the OER stability. Consequently, the HIr RuO catalyst shows an overpotential of 255 mV at 10 mA cm and displays exceptional catalytic endurance in acidic electrolytes, surpassing 1100 h, representing a remarkable one-order-of-magnitude increase in stability compared to that of pristine HIrO. A proton exchange membrane electrolyser utilizing the HIr RuO catalyst as an anode exhibits stable performance for more than 1280 h under a high current density of 2 A cm.

摘要

质子交换膜水电解槽有望开启清洁能源的新时代,但在设计用于酸性析氧反应(OER)的活性和耐用性电催化剂方面,它们仍然是一个巨大的障碍。在本研究中,引入了一种嵌入单原子分散钌原子的质子化氧化铱(HIr RuO),其在酸性水氧化中表现出卓越的活性和稳定性。单个Ru掺杂剂有利于在Ir─O晶格中诱导局部氧空位,协同增强OOH*中间体的吸附并提高本征OER活性。此外,Ru的优先氧化和氧空位的电负性显著稳定了Ir─O活性位点,提高了OER稳定性。因此,HIr RuO催化剂在10 mA cm时的过电位为255 mV,并且在酸性电解质中表现出卓越的催化耐久性,超过1100小时,与原始HIrO相比,稳定性显著提高了一个数量级。使用HIr RuO催化剂作为阳极的质子交换膜电解槽在2 A cm的高电流密度下表现出超过1280小时的稳定性能。

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