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Co@NCNT@ZnIn S 中定向电荷分离和转移引发的出乎意料的高光催化析氢性能。

Unexpected High-Performance Photocatalytic Hydrogen Evolution in Co@NCNT@ZnIn S Triggered by Directional Charge Separation and Transfer.

机构信息

Beijing Advanced Innovation Center for Materials Genome Engineering, Institute for Advanced Materials and Technology, University of Science and Technology Beijing, Beijing, 100083, China.

School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, 100083, China.

出版信息

Small. 2022 Dec;18(49):e2205266. doi: 10.1002/smll.202205266. Epub 2022 Oct 27.

Abstract

The structural design of photocatalysts is highly related to the separation and transfer of photogenerated carriers, which is essential for the improvement of photocatalytic hydrogen evolution performance. Here, the hybrid photocatalyst M@NCNT@ZIS (M: Fe, Co, Ni; NCNT: nitrogen-doped carbon nanotube; ZIS: ZnIn S ) with a hierarchical structure is rationally designed and precisely synthesized. The unique hollow structure with a large specific surface area offers abundant reactive sites, thus increasing the adsorption of reactants. Importantly, the properly positioned metal nanoparticles realize the directional charge migration from ZIS to M@NCNT, which significantly improves the efficiency of charge separation. Furthermore, the intimate interface between M@NCNT and ZIS effectively facilitates charge migration by shortening the transfer distance and providing numerous transport channels. As a result, the optimized Co@NCNT@ZIS exhibits a remarkable photocatalytic hydrogen evolution efficiency (43.73 mmol g h ) without Pt as cocatalyst. Experimental characterizations and density functional theory calculations demonstrate that the synergistic effect between hydrogen adsorption and interfacial charge transport is of great significance for improving photocatalytic hydrogen production performance.

摘要

光催化剂的结构设计与光生载流子的分离和转移密切相关,这对于提高光催化析氢性能至关重要。在这里,我们合理设计并精确合成了具有分级结构的混合光催化剂 M@NCNT@ZIS(M:Fe、Co、Ni;NCNT:氮掺杂碳纳米管;ZIS:ZnInS)。独特的中空结构具有较大的比表面积,提供了丰富的反应位点,从而增加了反应物的吸附。重要的是,适当定位的金属纳米颗粒实现了从 ZIS 到 M@NCNT 的定向电荷迁移,显著提高了电荷分离效率。此外,M@NCNT 和 ZIS 之间的紧密界面通过缩短传输距离和提供众多传输通道,有效地促进了电荷迁移。结果,优化后的 Co@NCNT@ZIS 在没有 Pt 作为共催化剂的情况下表现出显著的光催化析氢效率(43.73mmol g h)。实验表征和密度泛函理论计算表明,氢吸附和界面电荷输运之间的协同效应对提高光催化制氢性能具有重要意义。

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