Suppr超能文献

一种在酸性条件下合成用于析氧的高活性非晶态氧化铱的简单方法。

A Simple Method for Synthesizing Highly Active Amorphous Iridium Oxide for Oxygen Evolution under Acidic Conditions.

作者信息

Salimi Payam, Najafpour Mohammad Mahdi

机构信息

Department of Chemistry, Institute for Advanced Studies in Basic Sciences (IASBS), 45137-66731, Zanjan, Iran.

Centre of Climate Change and Global Warming, Institute for Advanced Studies in Basic Sciences (IASBS), 45137-66731, Zanjan, Iran.

出版信息

Chemistry. 2020 Dec 18;26(71):17063-17068. doi: 10.1002/chem.202000955. Epub 2020 Nov 30.

Abstract

Water splitting for hydrogen production has been recognized as a promising approach to store sustainable energy. The performance of this method is limited by the oxygen-evolution reaction. Herein, an approach for synthesizing a highly active oxygen-evolving catalyst by a one-step, low-cost, environmentally friendly, and easy-to-perform method is presented, which works by using iridium metal as the anode at a relatively high potential. The obtained IrO /Ir interface showed an overpotential of 250 mV at 10 mA cm in 0.1 m HClO and remained stable under electrochemical conditions. The IrO that was mechanically separated from the surface of IrO /Ir metal after operation showed a threefold increase in activity compared to the current benchmark IrO catalyst. Various characterization analyses were used to identify the structure and morphology of the catalyst, which suggested nanosized, porous, and amorphous IrO on the surface of metallic Ir. This synthetic approach can inspire a variety of opportunities to design and synthesize efficient metal oxide-based electrocatalysts for sustainable energy conversion and utilization.

摘要

水分解制氢已被认为是一种储存可持续能源的有前景的方法。该方法的性能受到析氧反应的限制。在此,提出了一种通过一步法、低成本、环境友好且易于实施的方法来合成高活性析氧催化剂的途径,该方法通过在相对较高的电位下使用铱金属作为阳极来实现。所获得的IrO₂/Ir界面在0.1 m HClO₄中10 mA cm⁻²时的过电位为250 mV,并且在电化学条件下保持稳定。操作后从IrO₂/Ir金属表面机械分离的IrO₂与当前的基准IrO₂催化剂相比,活性提高了三倍。使用各种表征分析来确定催化剂的结构和形态,结果表明在金属Ir表面存在纳米尺寸、多孔且无定形的IrO₂。这种合成方法可以激发设计和合成用于可持续能源转换和利用的高效金属氧化物基电催化剂的各种机会。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验