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基于石墨炔的ZnCdS和NiO双S型异质结促进光催化析氢

Graphdiyne based ZnCdS and NiO dual S-scheme heterojunction boosting photocatalytic hydrogen evolution.

作者信息

Li Bingzhu, Ma Xiaohua, Lei Minjun, Jin Zhiliang

机构信息

School of Chemistry and Chemical Engineering, Ningxia Key Laboratory of Solar Chemical Conversion Technology, Key Laboratory for Chemical Engineering and Technology, State Ethnic Affairs Commission, North Minzu University, Yinchuan 750021, PR China.

School of Chemistry and Chemical Engineering, Ningxia Key Laboratory of Solar Chemical Conversion Technology, Key Laboratory for Chemical Engineering and Technology, State Ethnic Affairs Commission, North Minzu University, Yinchuan 750021, PR China.

出版信息

J Colloid Interface Sci. 2025 Apr;683(Pt 1):1064-1077. doi: 10.1016/j.jcis.2024.12.150. Epub 2024 Dec 19.

Abstract

As a novel carbon-based material with two-dimensional (2D) characteristics, graphdiyne (GDY) shows great potential in constructing active catalytic sites due to its distinctive atomic configuration and sp/sp conjugated hybrid two-dimensional networks. In this study, the layered GDY was synthesized using the ball milling method, and ZnCdS/Graphdiyne/NiO (ZnCdS/GDY/NiO) composite was synthesized by in-situ composite and physical mixing method. The prepared ZnCdS/GDY/NiO has good photostability outstanding performance in photocatalytic hydrogen production. When exposed to 5 W of white light, the ZnCdS/GDY/NiO photocatalyst demonstrates a hydrogen production rate of 24.44 mmol·g·h, which was 8.4 times greater than that of pure ZnCdS under the same conditions. Various characterization tests and theoretical calculations show that the improved photocatalytic efficiency resulted from the formation of a dual S-scheme heterostructure in the ZnCdS/GDY/NiO composite catalyst, which promoted the recombination of relatively useless photogenerated electron holes. Furthermore, strong photogenerated holes and electrons in the more positive valence band (VB) and the more negative conduction band (CB) were retained, which significantly improved the photogenerated carrier separation ability of the composite catalyst, and thus enhances the hydrogen evolution activity.

摘要

作为一种具有二维(2D)特性的新型碳基材料,石墨炔(GDY)因其独特的原子构型和sp/sp共轭杂化二维网络,在构建活性催化位点方面显示出巨大潜力。在本研究中,采用球磨法合成了层状GDY,并通过原位复合和物理混合法合成了ZnCdS/石墨炔/NiO(ZnCdS/GDY/NiO)复合材料。制备的ZnCdS/GDY/NiO在光催化产氢方面具有良好的光稳定性和优异性能。当暴露于5W白光下时,ZnCdS/GDY/NiO光催化剂的产氢速率为24.44 mmol·g·h,是相同条件下纯ZnCdS产氢速率的8.4倍。各种表征测试和理论计算表明,ZnCdS/GDY/NiO复合催化剂中形成的双S型异质结构提高了光催化效率,促进了相对无用的光生电子空穴的复合。此外,在更正的价带(VB)和更负的导带(CB)中保留了强的光生空穴和电子,这显著提高了复合催化剂的光生载流子分离能力,从而增强了析氢活性。

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