高活性烧绿石型钌酸镨电催化剂用于有效的酸性水氧化。

IF 8.3 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Jinhui Zhang, Lei Shi*, Ruixue Tong and Liping Yang, 
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引用次数: 0

摘要

为了从水中直接生产可燃氢气,需要用于析氧反应(OER)的高活性、耐酸和经济的催化剂。本文提出了一种基于钌酸镨(Pr2Ru2O7)的电催化剂,该催化剂在酸性水氧化方面大大优于RuO2。具体而言,在10mA cm-2下,该电催化剂表现出213mV的低过电位(η)和显著优异的稳定性。此外,Pr2Ru2O7的转换频率(TOF)显著上升,本征质量活性为1618.8 a gRu-1(η=300 mV),超过了最常见的酸性OER催化剂。密度泛函理论计算和电子结构研究表明,该烧绿石中与Pr离子半径较大的Ru-O键相关的Ru 4d能带中心低于RuO2,这将优化吸附氧物种与催化金属位点之间的结合,提高催化本征活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Highly Active Pyrochlore-Type Praseodymium Ruthenate Electrocatalyst for Efficient Acid–Water Oxidation

Highly Active Pyrochlore-Type Praseodymium Ruthenate Electrocatalyst for Efficient Acid–Water Oxidation

To produce directly combustible hydrogen from water, highly active, acid-resistant, and economical catalysts for oxygen evolution reaction (OER) are needed. An electrocatalyst based on praseodymium ruthenate (Pr2Ru2O7) is presented here that greatly outperforms RuO2 for acid–water oxidation. Specifically, at 10 mA cm–2, this electrocatalyst presents a low overpotential (η) of 213 mV and markedly superior stability. Moreover, Pr2Ru2O7 presents a significant rise in turnover frequency (TOF) and a highly intrinsic mass activity of 1618.8 A gRu–1 (η = 300 mV), exceeding the most commonly reported acid OER catalysts. Density functional theory calculations and electronic structure study demonstrate that the Ru 4d-band center related to the longer Ru–O bond with a large radius of Pr ion in this pyrochlore is lower than that in RuO2, which would optimize the binding between the adsorbed oxygen species and catalytic metal sites and enhance the catalytic intrinsic activity.

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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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