电催化剂
材料科学
整体
化学工程
析氧
分解水
过渡金属
纳米技术
催化作用
纳米线
电化学
电极
化学
物理化学
有机化学
光催化
工程类
作者
Fang Yang,Tuzhi Xiong,Peng Huang,Shuhui Zhou,Qirong Tan,Hao Yang,Yongchao Huang,Muhammad‐Sadeeq Balogun
标识
DOI:10.1016/j.cej.2021.130279
摘要
Different transition metal compounds (TMCs) nanostructures grown on conductive substrates have been considered as promising self-supportive non-precious electrocatalysts for electrochemical water splitting, but extremely challenging to develop facile and generalized approaches for rational design and enhancing their catalytic properties. Herein, we develop a general strategy to boost the hydrogen and oxygen evolution reactions (HER and OER) performance of TMCs by designing monolith electrocatalyst architectures. The monoliths comprises of TMCs integrated on carbon fiber cloth core–shell ([email protected]) structure. The [email protected] allows the creation of numerous lattice distortions and strong electronic interactions between [email protected] and metal cations of the TMCs. Such lattice distortions exposes more active sites in [email protected]/TMCs compared to the pristine CFC coated TMCs (CFC/TMC). Cobalt phosphide (CoP) nanowires and NiFe-LDH coated on [email protected] exhibits the optimized HER and OER activities. Overall water splitting device assembled based on the optimized HER and OER electrodes also achieve low overall potential of 1.53 V at 10 mA cm−2. More importantly, we further experimentally verify that the integration of Ni3N and Ni3S2, CoS2, NiCo-LDH, NiMn-LDH with [email protected] also reveal similar improved performance, providing a general and valuable strategy into the design of other self-supporting electrocatalysts for water splitting and beyond.
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