分解水
析氧
材料科学
双功能
反键分子轨道
无定形固体
纳米棒
纳米技术
化学工程
可逆氢电极
催化作用
结晶学
电化学
电极
物理化学
化学
生物化学
物理
光催化
量子力学
参比电极
原子轨道
电子
工程类
作者
Linfeng Li,Huachuan Sun,Xuefei Xu,Muhammad Humayun,Xiang Ao,Muk Fung Yuen,Xinying Xue,Ying Wu,Yang Yang,Chundong Wang
标识
DOI:10.1021/acsami.2c13417
摘要
The design of bifunctional electrocatalysts for hydrogen and oxygen evolution reactions delivering excellent catalytic activity and stability is highly desirable, yet challenged. Herein, we report an amorphous RuO2-encapsulated crystalline Ni0.85Se nanorod structure (termed as a/c-RuO2/Ni0.85Se) for enhanced HER and OER activities. The as-prepared a/c-RuO2/Ni0.85Se nanorods not only demonstrate splendid HER activity (58 mV@10 mA cm-2 vs RHE), OER activity (233 mV@10 mA cm-2 vs RHE), and electrolyzer activity (1.488 V@10 mA cm-2 vs RHE for overall water splitting) but also exhibit long-term stability with negligible performance decay after 50 h continuous test for overall water splitting. In addition, the variation of the d-band center (from the perspective of bonding and antibonding states) is unveiled theoretically by density functional theory calculations upon amorphous RuO2 layers coupling to clarify the increased hydrogen species adsorption for HER activity enhancement. This work represents a new pathway for the fabrication of bifunctional electrocatalysts toward green hydrogen generation.
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