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用于质子交换膜电解的具有高质量比析氧活性的IrO纳米颗粒修饰的Ir掺杂WO纳米线

IrO Nanoparticle-Decorated Ir-Doped WO Nanowires with High Mass Specific OER Activity for Proton Exchange Membrane Electrolysis.

作者信息

Yan Tianqing, Chen Shiyi, Sun Wendi, Liu Yuezheng, Pan Lun, Shi Chengxiang, Zhang Xiangwen, Huang Zhen-Feng, Zou Ji-Jun

机构信息

Key Laboratory for Green Chemical Technology of the Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin300072, China.

Collaborative Innovative Center of Chemical Science and Engineering (Tianjin), Tianjin300072, China.

出版信息

ACS Appl Mater Interfaces. 2023 Feb 8;15(5):6912-6922. doi: 10.1021/acsami.2c20529. Epub 2023 Jan 30.

Abstract

The oxygen evolution reaction (OER) severely limits the efficiency of proton exchange membrane (PEM) electrolyzers due to slow reaction kinetics. IrO is currently a commonly used anode catalyst, but its large-scale application is limited due to its high price and scarce reserves. Herein, we reported a practical strategy to construct an acid OER catalyst where Iridium oxide loading and iridium element bulk doping are realized on the surface and inside of WO nanowires by immersion adsorption, respectively. Specifically, WIrO has an overpotential of 278 mV at 10 mA·cm in 0.1 M HClO. The mass activity of 714.10 A·g at 1.53 V vs. the reversible hydrogen electrode (RHE) is 80 times that of IrO, and it can run stably for 55 h. In the PEM water electrolyzer device, its mass activity reaches 3563.63 A·g at the cell voltage of 2.0 V. This improved catalytic performance is attributed to the following aspects: (1) The electron transport between iridium and tungsten effectively improves the electronic structure of the catalyst; (2) the introduction of iridium into WO by means of elemental bulk doping and nanoparticles supporting for the enhanced conductivity and electrochemically active surface area of the catalyst, resulting in extensive exposure of active sites and increased intrinsic activity; and (3) during the OER process, partial iridium elements in the bulk phase are precipitated, and iridium oxide is formed on the surface to maintain stable activity. This work provides a new idea for designing oxygen evolution catalysts with low iridium content for practical application in PEM electrolyzers.

摘要

析氧反应(OER)由于反应动力学缓慢,严重限制了质子交换膜(PEM)电解槽的效率。氧化铱目前是一种常用的阳极催化剂,但其大规模应用因价格高昂和储量稀缺而受到限制。在此,我们报道了一种构建酸性OER催化剂的实用策略,通过浸渍吸附分别在WO纳米线的表面和内部实现氧化铱负载和铱元素体相掺杂。具体而言,WIrO在0.1 M HClO中,在10 mA·cm²时的过电位为278 mV。相对于可逆氢电极(RHE),在1.53 V时的质量活性为714.10 A·g,是氧化铱的80倍,并且可以稳定运行55小时。在PEM水电解槽装置中,在2.0 V的电池电压下其质量活性达到3563.63 A·g。这种催化性能的提升归因于以下几个方面:(1)铱和钨之间的电子传输有效地改善了催化剂的电子结构;(2)通过元素体相掺杂和纳米颗粒负载将铱引入WO,增强了催化剂的导电性和电化学活性表面积,导致活性位点大量暴露并提高了本征活性;(3)在OER过程中,体相中的部分铱元素沉淀,在表面形成氧化铱以维持稳定的活性。这项工作为设计低铱含量的析氧催化剂以在PEM电解槽中实际应用提供了新思路。

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