电催化剂
六方晶系
退火(玻璃)
过渡金属
透射电子显微镜
催化作用
化学
试剂
纳米材料
材料科学
密度泛函理论
吸附
纳米技术
电化学
化学物理
结晶学
氢
计算化学
物理化学
电极
有机化学
复合材料
作者
Yuanmeng Zhao,Hengjiang Cong,Peng Li,Dean Wu,Shengli Chen,Wei Luo
标识
DOI:10.1002/anie.202016207
摘要
Abstract Layered transition metal dichalcogenide (TMD) nanomaterials are promising alternatives to platinum (Pt) for the hydrogen evolution reaction (HER). However, the family of layered TMDs is mainly limited to Group IV–VII transition metals, while the synthesis of layered TMDs based on metals from other groups still remains a challenge. Herein, we demonstrate by atomic‐resolution transmission electron microscopy that hexagonal RuSe 2 ( h ‐RuSe 2 ) nanosheets with a mixture of 2H and 1T phases can be obtained by a facile bottom‐up colloidal synthetic approach. The obtained h ‐RuSe 2 , which can be transformed into the thermodynamically favorable phase of cubic RuSe 2 ( c ‐RuSe 2 ) only after annealing at 600 °C, exhibits Pt‐like HER performance, with a fivefold turnover frequency enhancement compared to the c ‐RuSe 2 in alkaline media. Experimental results and density functional theory (DFT) calculations reveal that the enhanced adsorption free energies of H 2 O (Δ G ), optimized adsorption free energies of H (Δ G H* ), and increased conductivity of h ‐RuSe 2 contribute to its superior HER activity.
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