材料科学
亚稳态
分解水
催化作用
离解(化学)
相(物质)
化学物理
化学工程
纳米技术
六角相
氢
六方晶系
结晶学
物理化学
工程类
物理
光催化
量子力学
有机化学
化学
生物化学
作者
Guijuan Wei,Yongli Shen,Xixia Zhao,Ying Wang,Weiqing Zhang,Changhua An
标识
DOI:10.1002/adfm.202109709
摘要
Abstract In addition to tuning the size and shape, exploring highly efficient and cost‐effective catalysts with active metastable phase represents an alternative strategy to improve electrocatalytic water splitting performance. However, it still remains a big challenge to synthesize unconventional crystal structures under mild conditions. Herein, a facile CH 4 plasma assisted strategy to synthesize hexagonal close‐packed (hcp) Ni 3 Fe/C porous nanosheets by in situ topology reduction of Ni 3 Fe‐LDH nanosheets is successfully developed. Compared with its face‐centered cubic phase counterpart (fcc‐Ni 3 Fe/C), the resulting hcp‐Ni 3 Fe/C catalyst exhibits much enhanced activity with overpotentials of 70 and 201 mV at a current density of 10 mA cm −2 for the hydrogen evolution reaction and oxygen evolution reaction, respectively. Moreover, a small cell voltage of 1.54 V is realized to drive overall water splitting. Theoretical calculations further reveal that hcp‐Ni 3 Fe allows energetically favorable adsorption and dissociation of H 2 O molecules. This work presents a new strategy for designing advanced metastable phase electrocatalysts with high performance for energy and environmentally relevant reactions.
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