材料科学
双功能
掺杂剂
钴
分解水
纳米片
析氧
电催化剂
化学工程
兴奋剂
催化作用
密度泛函理论
纳米技术
蚀刻(微加工)
纳米复合材料
结合能
过渡金属
电化学
无机化学
物理化学
计算化学
电极
化学
光电子学
有机化学
冶金
核物理学
工程类
物理
图层(电子)
光催化
作者
Danna Song,Jikai Sun,Lanju Sun,Shengliang Zhai,Ghim Wei Ho,Hao Wu,Wei Deng
标识
DOI:10.1002/aenm.202100358
摘要
Abstract Facile synthesis of elaborate nanostructured transition metal compounds with tunable components remains challenging because multiple synthetic procedures or complex manipulation are normally involved. Herein, an acid‐etching strategy is applied to Co, in which the composition and morphology of the resultant materials are tunable. Specifically, a novel two‐tiered Co(CO 3 ) 0.5 (OH)·0.11H 2 O nanosheet is formed, part of which decomposes to produce hierarchical Co(CO 3 ) 0.5 (OH)·0.11H 2 O/Co 3 O 4 nanocomposite by tuning the etching condition. The composite shows bifunctional electrocatalytic capability towards the oxygen evolution and hydrogen evolution reactions (OER and HER). Moreover, the phosphorous dopant is introduced to boost the catalytic activity, especially in the HER. Density functional theory calculations reveal that the phosphorous dopant can dramatically push the binding energy to the ideal value, thus improving the HER performance. Computed results indicate that partial orbitals of the P atom are above the Fermi level and the P atom enhances the charge density of the neighboring Co atom, which optimizes the H* binding. In addition, an efficient overall water splitting configuration is performed with the integration of the P‐doped Co compound catalysts. The acid‐etching methodology inspires more novel nanostructured and multicomponent metal compounds for prominent electrocatalysis.
科研通智能强力驱动
Strongly Powered by AbleSci AI