过电位
塔菲尔方程
材料科学
石墨烯
氧化物
电催化剂
纳米技术
化学工程
分解水
掺杂剂
纳米复合材料
兴奋剂
催化作用
化学
电化学
电极
光电子学
冶金
物理化学
光催化
工程类
生物化学
作者
Xiaodong Hao,Tingting Wei,Qin Ma,Yuhao Zhou,Yang� Yang,Yi Jing,Xinyi Feng,Xishuo Zhang,Jin Zhang,Deqiang Yin,Zhen‐Hong He,Shufang Ma,Bingshe Xu
标识
DOI:10.1021/acsanm.3c05193
摘要
The advancement of cost-effective and highly efficient electrocatalysts for hydrogen evolution is pivotal in fostering the progress of clean energy technologies. In this study, we present a reforming approach aimed at facile fabrication of the Cr-CeO2/rGO electrocatalyst. This involves incorporating a limited quantity of reduced graphene oxide (rGO) to serve as a conductive scaffold for CeO2 nanocrystals (NCs) while also introducing Cr, a transition metal, as an active dopant. It is found that the introduction of Cr and rGO induces charge transfer, leading to enhanced electrical conductivity and the creation of additional active sites on the nanocomposite surface. The synergy between rGO and CeO2, along with Cr doping in CeO2, significantly improves HER performance. The representative sample of the Cr(5%)-CeO2/rGO catalyst demonstrates a low overpotential of 83 mV at a current density of 10 mA cm–2, a low Tafel slope of 81 mV dec–1, and excellent stability under alkaline conditions. Significantly, this value of overpotential is reduced by 81 and 127 mV compared to those of the CeO2/rGO nanocomposites and the pristine CeO2 NCs. Theoretical density functional theory calculations additionally validate the phenomenon of charge transfer and improved HER properties, with Cr-CeO2 displaying a favorable Gibbs free energy (ΔGH*) for H* adsorption. This study offers novel insights into the design of precious metal electrocatalysts featuring functional interfaces and a wealth of active sites, holding great promise for industrial applications in clean energy conversion and storage.
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