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过渡金属单原子锚定在 MoS 上用于增强 g-CN 光催化剂的光催化析氢性能。

Transition-Metal Single Atom Anchored on MoS for Enhancing Photocatalytic Hydrogen Production of g-CN Photocatalysts.

机构信息

State Key Laboratory of Chemical Engineering, School of Chemical Engineering, East China University of Science and Technology, Shanghai 200237, China.

State Key Laboratory Incubation Base for Green Processing of Chemical Engineering, School of Chemistry and Chemical Engineering, Shihezi University, Shihezi 832003, Xinjiang, China.

出版信息

ACS Appl Mater Interfaces. 2023 Jun 7;15(22):26670-26681. doi: 10.1021/acsami.3c02895. Epub 2023 May 23.

Abstract

Single-atom catalyst technology with near-100% atomic utilization and a well-defined coordination structure has provided new ideas for designing high-performance photocatalysts, which is also beneficial for reducing the usage of noble metal cocatalysts. Herein, a series of single-atomic MoS-based cocatalysts where monoatomic Ru, Co, or Ni modify MoS (SA-MoS) for enhancing the photocatalytic hydrogen production performance of g-CN nanosheets (NSs) are rationally designed and synthesized. The 2D SA-MoS/g-CN photocatalysts with Ru, Co, or Ni single atoms show similar enhanced photocatalytic activity, and the optimized Ru-MoS/g-CN photocatalyst has the highest hydrogen production rate of 11115 μmol/h/g, which is about 37 and 5 times higher than that of pure g-CN and MoS/g-CN photocatalysts, respectively. Experimental and density functional theory calculation results reveal that the enhanced photocatalytic performance is mainly attributed to the synergistic effect and intimate interface between SA-MoS with well-defined coordination single-atomic structures and g-CN NSs, which is conducive to the rapid interfacial charge transport, and the unique single-atomic structure of SA-MoS with modified electronic structure and appropriate hydrogen adsorption performance offers abundant reactive sites for enhancing the photocatalytic hydrogen production performance. This work provides new insight into improving the cocatalytic hydrogen production performance of MoS by a single-atomic strategy.

摘要

单原子催化剂技术具有近 100%的原子利用率和明确的配位结构,为设计高性能光催化剂提供了新思路,也有利于减少贵金属共催化剂的使用。在此,设计并合理合成了一系列单原子 MoS 基共催化剂,其中单原子 Ru、Co 或 Ni 修饰 MoS(SA-MoS)以增强 g-CN 纳米片(NSs)的光催化析氢性能。具有 Ru、Co 或 Ni 单原子的 2D SA-MoS/g-CN 光催化剂表现出相似的增强光催化活性,优化的 Ru-MoS/g-CN 光催化剂具有最高的制氢速率 11115 μmol/h/g,分别是纯 g-CN 和 MoS/g-CN 光催化剂的 37 倍和 5 倍。实验和密度泛函理论计算结果表明,增强的光催化性能主要归因于具有明确配位单原子结构的 SA-MoS 与 g-CN NSs 之间的协同效应和紧密界面,有利于快速的界面电荷传输,以及具有改性电子结构和适当氢吸附性能的独特单原子结构为增强光催化析氢性能提供了丰富的反应活性位。这项工作为通过单原子策略提高 MoS 的共催化析氢性能提供了新的见解。

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