镍
硒化物
催化作用
碳纳米管
耐久性
材料科学
吸附
纳米颗粒
密度泛函理论
动力学
化学工程
纳米技术
冶金
化学
计算化学
复合材料
物理化学
硒
工程类
有机化学
物理
量子力学
作者
Hongyao Xue,Tongqing Yang,Ziming Zhang,Yi-Xue Zhang,Zhihong Geng,Yan He
标识
DOI:10.1016/j.apcatb.2023.122641
摘要
We present an electrodeposition strategy to construct heterostructures nickel selenide (NiSe) and carbon nanotubes (CNTs), namely NiSe@CNTs, to tune the electronic structure of the Ni sites, thus stimulating the hidden catalytic potential of the Ni sites. As expected, the optimized NiSe@CNTs exhibits unprecedentedly ultra-high activity for HER (27 mV at 10 mA cm−2) and OER (145 mV at 100 mA cm−2) and outstanding long-term durability (730 h). Based on the systematic characterization and DFT results, the Ni sites with increased electron density induced by π-electron off-domain of CNTs not only greatly optimize the H* adsorption kinetics but also reduce the energy barrier of the *O→*OOH step, demonstrating the enhanced intrinsic catalytic activity. Furthermore, the introduced CNTs not only avoid aggregation of nanoparticles but also reduce particle size, thus increasing the number of exposed Ni active sites. This study provides guidance for the exploration of catalysts with ultra-high activity and durability.
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