Wang Yahui, Hao Shaoyun, Liu Xiangnan, Wang Qiqi, Su Zhiwei, Lei Lecheng, Zhang Xingwang
Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University, Zheda Road 38, Hangzhou, Zhejiang 310027, China.
Institute of Zhejiang University-Quzhou, 78 Jiuhua Boulevard North, Quzhou, Zhejiang 324000, China.
ACS Appl Mater Interfaces. 2020 Aug 19;12(33):37006-37012. doi: 10.1021/acsami.0c00389. Epub 2020 Aug 6.
Electrocatalytic water splitting in acidic media based on a proton-exchange membrane (PEM) is a promising technique for the large-scale production of hydrogen. However, developing electrocatalysts with high activity and excellent stability for an oxygen evolution reaction (OER) in acidic media is still a big challenge. Herein, a Ce-IrO catalyst supported on N-doped porous carbon (NPC) was developed via doping Ce into IrO nanoparticles. The Ce-IrO nanoparticles were uniformly distributed on NPC due to the high surface area. The optimized Ce-IrO@NPC delivers a low overpotential of 224 mV and excellent stability of 100 h in 0.5 M HSO at 10 mA cm. Density functional theory (DFT) calculations indicated that the introduction of Ce could modify the electronic structure of IrO, decreasing the energy barrier of the rate-determining step for OER and enhancing the electrochemical OER performance. Our work opens up a new way of developing anodic electrocatalysts, which can be stably applied in acidic media.
基于质子交换膜(PEM)的酸性介质中的电催化水分解是大规模制氢的一项很有前景的技术。然而,开发在酸性介质中对析氧反应(OER)具有高活性和优异稳定性的电催化剂仍然是一个巨大的挑战。在此,通过将Ce掺杂到IrO纳米颗粒中,开发了一种负载在氮掺杂多孔碳(NPC)上的Ce-IrO催化剂。由于高比表面积,Ce-IrO纳米颗粒均匀分布在NPC上。优化后的Ce-IrO@NPC在0.5 M HSO中于10 mA cm下具有224 mV的低过电位和100 h的优异稳定性。密度泛函理论(DFT)计算表明,Ce的引入可以改变IrO的电子结构,降低OER速率决定步骤的能垒并提高电化学OER性能。我们的工作开辟了一种开发阳极电催化剂的新途径,该催化剂可稳定应用于酸性介质中。