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高性能负载型氢氧化氧铱水氧化电催化剂。

High-Performance Supported Iridium Oxohydroxide Water Oxidation Electrocatalysts.

作者信息

Massué Cyriac, Pfeifer Verena, Huang Xing, Noack Johannes, Tarasov Andrey, Cap Sébastien, Schlögl Robert

机构信息

Department of Inorganic Chemistry, Fritz Haber Institute of the Max Planck Society, Faradayweg 4-6, 14195, Berlin, Germany.

Department of Heterogenous Reactions, Max Planck Institute for Chemical Energy Conversion, Stiftstrasse 34-36, 45470, Mülheim-an-der-Ruhr, Germany.

出版信息

ChemSusChem. 2017 May 9;10(9):1943-1957. doi: 10.1002/cssc.201601817. Epub 2017 Mar 30.

Abstract

The synthesis of a highly active and yet stable electrocatalyst for the anodic oxygen evolution reaction (OER) remains a major challenge for acidic water splitting on an industrial scale. To address this challenge, we obtained an outstanding high-performance OER catalyst by loading Ir on conductive antimony-doped tin oxide (ATO)-nanoparticles by a microwave (MW)-assisted hydrothermal route. The obtained Ir phase was identified by using XRD as amorphous (XRD-amorphous), highly hydrated Ir oxohydroxide. To identify chemical and structural features responsible for the high activity and exceptional stability under acidic OER conditions with loadings as low as 20 μg  cm , we used stepwise thermal treatment to gradually alter the XRD-amorphous Ir phase by dehydroxylation and crystallization of IrO . This resulted in dramatic depletion of OER performance, indicating that the outstanding electrocatalytic properties of the MW-produced Ir oxohydroxide are prominently linked to the nature of the produced Ir phase. This finding is in contrast with the often reported stable but poor OER performance of crystalline IrO -based compounds produced through more classical calcination routes. Our investigation demonstrates the immense potential of Ir oxohydroxide-based OER electrocatalysts for stable high-current water electrolysis under acidic conditions.

摘要

合成一种用于阳极析氧反应(OER)的高活性且稳定的电催化剂,对于工业规模的酸性水分解而言仍然是一项重大挑战。为应对这一挑战,我们通过微波(MW)辅助水热法将铱负载在导电的锑掺杂氧化锡(ATO)纳米颗粒上,从而获得了一种出色的高性能OER催化剂。通过X射线衍射(XRD)确定所得到的铱相为非晶态(XRD非晶态)的高度水合铱羟基氧化物。为了确定在低至20μg cm负载量的酸性OER条件下,导致高活性和卓越稳定性的化学和结构特征,我们采用逐步热处理的方法,通过IrO的脱羟基化和结晶来逐渐改变XRD非晶态铱相。这导致OER性能急剧下降,表明微波制备的铱羟基氧化物出色的电催化性能与所生成铱相的性质密切相关。这一发现与通常报道的通过更传统的煅烧路线制备的基于晶态IrO的化合物稳定但OER性能较差的情况形成对比。我们的研究表明,基于铱羟基氧化物的OER电催化剂在酸性条件下用于稳定的高电流水电解具有巨大潜力。

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