首页|钇掺杂二氧化铱用于高效酸性电化学析氧反应

钇掺杂二氧化铱用于高效酸性电化学析氧反应

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酸性质子交换膜电解水(PEMWE)是一种电流密度高、动态响应快、产氢纯度高的电解水工艺,为实现其高效工业级应用,开发廉价、高效、稳定的析氧催化剂尤为关键.本文通过两步合成法将稀土元素钇(Y)掺杂到无定形的碳载体中修饰其表面的二氧化铱(IrO2)颗粒.制备得到的IrO2/YxC具有优异的酸性析氧反应催化活性,在10mA/cm2 的电流密度下所需过电位仅为270mV,低于未掺杂Y的IrO2/C(300mV)以及商用IrO2(310mV).Y的掺杂强化了碳载体与其表面二氧化铱颗粒之间的金属-载体相互作用,导致了Ir活性位点周围电子密度的变化,有利于调节反应中间体的吸附,优化反应速率.这一研究成果为PEMWE中析氧过程提供了新的催化剂设计思路,有望推动PEMWE技术在清洁能源领域更广泛的应用.
Yttrium doped iridium dioxide for efficient acidic electrochemical oxygen evolution reaction
Proton exchange membrane water electrolysis(PEMWE)is a water electrolysis process with high current density,fast dynamic response and high hydrogen purity.To achieve its efficient industrial application,the development of inexpensive,efficient and stable oxygen evolution catalysts is particularly important.In this paper,a two-step synthesis method was used to dope the rare earth element yttrium(Y)into amorphous carbon supports to modify the surface of iridium dioxide(IrO2)particles.The prepared IrO2/YxC exhibited excellent catalytic activity for the acidic oxygen evolution reaction with a required overpotential of only 270mV at a current density of 10mA/cm2,which was lower than that of undoped IrO2/C(300mV)and commercial IrO2(310mV).The enhancement of the metal carrier interaction between the carbon carrier and its surface iridium dioxide particles by Y doping led to changes in the electron density around the Ir active site,thereby facilitating the regulation of the adsorption of reaction intermediates and optimizing the reaction rate.This research provided a new catalyst design approach for the oxygen evolution process in PEMWE,and was expected to promote the wider application of PEMWE technology in the field of clean energy.

proton exchange membrane water electrolysisoxygen evolution reactioniridium dioxide catalystrare earth element yttriummetal-carrier interaction

刘振宇、沈紫晨、曹东、郭晓燕

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中国石油化工股份有限公司茂名分公司研究院,广东 茂名 525000

北京化工大学化学工程学院,北京 100029

质子交换膜电解水 析氧反应 二氧化铱催化剂 稀土元素钇 金属-载体相互作用

2024

化工进展
中国化工学会,化学工业出版社

化工进展

CSTPCD北大核心
影响因子:1.062
ISSN:1000-6613
年,卷(期):2024.43(12)