过电位
析氧
材料科学
电催化剂
石墨烯
电化学
电解质
密度泛函理论
化学工程
氧化还原
纳米技术
电极
物理化学
化学
计算化学
冶金
工程类
作者
Xiaoju Cui,Pengju Ren,Chao Ma,Jia Zhao,Ruixue Chen,Shiming Chen,N. Pethan Rajan,Haobo Li,Liang Yu,Zhong‐Qun Tian,Dehui Deng
标识
DOI:10.1002/adma.201908126
摘要
Abstract RuO 2 is considered as the state‐of‐the‐art electrocatalyst for the oxygen evolution reaction (OER) in acidic media. However, its practical application is largely hindered by both the high reaction overpotential and severe electrochemical corrosion of the active centers. To overcome these limitations, innovative design strategies are necessary, which remains a great challenge. Herein, robust interface Ru centers between RuO 2 and graphene, via a controllable oxidation of graphene encapsulating Ru nanoparticles, are presented to efficiently enhance both the activity and stability of the acidic OER. Through precisely controlling the reaction interface, a much lower OER overpotential of only 227 mV at 10 mA cm −2 in acidic electrolyte, compared with that of 290 mV for commercial RuO 2 , but a significantly higher durability than the commercial RuO 2 , are achieved. Density functional theory (DFT) calculations reveal that the interface Ru centers between the RuO 2 and the graphene can break the classic scaling relationships between the free energies of HOO* and HO* to reduce the limiting potential, rendering an enhancement in the intrinsic OER activity and the resistance to over‐oxidation and corrosion for RuO 2 .
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