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通过自组装构建具有 II 型和 Z 型异质结的 NiS@ZIS@CN 光催化剂用于高效光催化析氢。

Construction of NiS@ZIS@CN photocatalyst with type II and Z-type heterojunctions by self-assembly for efficient photocatalytic hydrogen evolution.

机构信息

Guangdong Provincial Key Laboratory of Quantum Engineering and Quantum Materials, Guangdong Engineering Technology Research Center of Efficient Green Energy and Environmental Protection Materials, School of Physics, School of Electronic and Information Engineering, South China Normal University, Guangzhou, 510006, PR China.

Guangdong Provincial Key Laboratory of Quantum Engineering and Quantum Materials, Guangdong Engineering Technology Research Center of Efficient Green Energy and Environmental Protection Materials, School of Physics, School of Electronic and Information Engineering, South China Normal University, Guangzhou, 510006, PR China.

出版信息

Environ Res. 2024 May 1;248:118302. doi: 10.1016/j.envres.2024.118302. Epub 2024 Jan 24.

Abstract

A novel ternary photocatalyst NiS@ZIS@CN with type II and Z-type heterojunctions was synthesized for the first time by hydrothermal and electrostatic self-assembly methods, effectively avoiding the thermal decomposition of CN during the synthesis of the complex. The best ternary catalyst NiS@ZIS@CN is capable of achieving an optimal hydrogen evolution rate of 9750 mmol g h, which is approximately 10.89 times as high as that of CN, indicating that the complex effectively enhanced the photocatalytic properties of the monomer. The coexistence of two types of heterojunctions in the complex effectively enhances photocatalytic performance, in which the monomer ZIS constructs type II scheme with NiS and Z-type scheme with CN, respectively. The two heterojunctions complement each other and jointly promote the rapid electron transfer from NiS and CN to the ZIS surface. In conclusion, the cooperation of the two heterojunctions efficiently facilitates the migration of photogenerated carriers, thus enhancing the photocatalytic hydrogen generation performance of NiS@ZIS@CN.

摘要

一种新型三元光催化剂 NiS@ZIS@CN 通过水热和静电自组装方法首次合成,有效地避免了在复合物合成过程中 CN 的热分解。最佳三元催化剂 NiS@ZIS@CN 能够实现 9750 mmol g h 的最佳析氢速率,约为 CN 的 10.89 倍,表明该复合物有效地增强了单体的光催化性能。复合物中两种异质结的共存有效地增强了光催化性能,其中单体 ZIS 分别与 NiS 构建了 II 型方案和与 CN 构建了 Z 型方案。这两种异质结相互补充,共同促进电子从 NiS 和 CN 快速转移到 ZIS 表面。总之,两种异质结的协同作用有效地促进了光生载流子的迁移,从而提高了 NiS@ZIS@CN 的光催化产氢性能。

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