Enhanced bifunctional photocatalytic performances for H2 evolution and HCHO elimination with an S-scheme CoWO4/CdIn2S4 heterojunction

IF 13.5 2区 化学 Q1 CHEMISTRY, PHYSICAL
Chengxin Chen , Hongfei Shi , Xiaoyan Cai , Liang Mao , Zhe Chen
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Abstract

Designing and establishing dual-functional S-scheme heterojunction photocatalysts with efficient separation of photoproduced carriers and intense oxidation/reduction capabilities holds immense practical value for their photocatalytic application in energy conversion and environmental purification. Herein, a novel series of x% CoWO4/CdIn2S4 (x% reflects the weight ratio of CWO to CIS; x = 10, 20, 30, 40 and 50) composites have been systematically designed and synthesized via electrospinning technique and hydrothermal methods. Their photocatalytic properties were assessed through HCHO removal and H2 generation under visible light. As anticipated, the optimized 30 % CWO/CIS heterojunction presented an outstanding H2 generation performance of 865.14 μmol g−1 h−1 with AQE = 3.6 % at λ = 420 nm, and achieved a 69 % removal percentage for HCHO within 1 h. Meanwhile, the pathway of HCHO degradation was presented based on in situ diffuse reflectance infrared Fourier transform spectroscopy (in situ DRIFTS) technique. The great catalytic performance was primarily ascribed to the enhancement in the visible–light absorption, number of active sites, and the construction of S-scheme heterojunction. Furthermore, the S-scheme charge transfer mechanism for the CWO/CIS catalyst system has been confirmed by in situ X–ray photoelectron spectroscopy (in situ XPS), electron spin resonance data, radical capturing experiments, and density functional theory (DFT) calculations. This research contributes valuable understanding for the systematic design and development of bifunctional S-scheme heterojunctions for gaseous pollutants removal and H2 production.

Abstract Image

S-scheme CoWO4/CdIn2S4异质结增强了H2演化和HCHO去除的双功能光催化性能
设计和建立具有高效分离光生载体和强氧化/还原能力的双功能s型异质结光催化剂,对其在能量转化和环境净化方面的光催化应用具有重要的实用价值。在这里,一个新的x% CoWO4/CdIn2S4系列(x%反映了CWO与CIS的重量比;采用静电纺丝技术和水热法制备了X = 10、20、30、40和50)复合材料。通过在可见光下脱除HCHO和生成H2来评价它们的光催化性能。结果表明,优化后的30% CWO/CIS异质结在λ = 420 nm处的产氢性能为865.14 μmol g−1 h−1,AQE = 3.6%,在1 h内对HCHO的去除率达到69%。同时,基于原位漫反射红外傅立叶变换光谱(in situ DRIFTS)技术,提出了HCHO降解的途径。其优异的催化性能主要归因于可见光吸收的增强、活性位点的增加和s型异质结的构建。此外,通过原位x射线光电子能谱(in situ XPS)、电子自旋共振数据、自由基捕获实验和密度泛函数理论(DFT)计算证实了CWO/CIS催化剂体系的S-scheme电荷转移机制。该研究为系统设计和开发用于去除气态污染物和制氢的双功能s型异质结提供了有价值的认识。
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来源期刊
物理化学学报
物理化学学报 化学-物理化学
CiteScore
16.60
自引率
5.50%
发文量
9754
审稿时长
1.2 months
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