Structurally designable Bi2S3/P-doped ZnO S-scheme photothermal metamaterial enhanced CO2 reduction

被引:14
|
作者
Pan, Longkai [1 ]
Yao, Li [1 ]
Mei, Hui [1 ]
Liu, Hongxia [1 ]
Jin, Zhipeng [1 ]
Zhou, Shixiang [1 ]
Zhang, Minggang [1 ]
Zhu, Gangqiang [2 ]
Cheng, Laifei [1 ]
Zhang, Litong [1 ]
机构
[1] Northwestern Polytech Univ, Sch Mat Sci & Engn, Sci & Technol Thermostructural Composite Mat Lab, Xian 710072, Shaanxi, Peoples R China
[2] Shaanxi Normal Univ, Sch Phys & Informat Technol, Xian 710062, Peoples R China
关键词
ZnO precursor slurry; 3D metamaterials; S-scheme; Photothermal effect; CO2; reduction; PHOTOCATALYTIC ACTIVITY; QUANTUM DOTS;
D O I
10.1016/j.seppur.2023.123365
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In this study, a novel 3D Bi2S3/P-ZnO S-scheme gyroid metamaterial was prepared by 3D printing and the hy-drothermal method. The unique gyroid macrostructure and nanoarray microstructure offer a large volume of active sites for the photothermal catalytic reaction, thus improving the overall utilization rate of light. ZnO obtained by sintering the precursor produces oxygen vacancies, primarily due to P doping. This enables it to have a photothermal effect. After loading Bi2S3, the photothermal effect of P-ZnO and Bi2S3 is coupled, further increasing the surface temperature of composite structure and speeding up the reaction rate. P-ZnO and Bi2S3 formed a S-scheme heterojunction, promoting the separation and transfer of photogenerated carriers. Under simulated sunlight, the CO and CH4 yield of Bi2S3/P-ZnO S-scheme gyroid metamaterials are 8.87 and 1.49 mu mol h-1. These are 3.45 times and 4.65 times of P-ZnO gyroid structure, respectively. Through SEM, TEM, XPS, ESR and in-situ FTIR characterizations, the transfer paths of photogenerated carriers between heterojunctions were revealed, and the reaction paths of photothermal catalytic CO2 reduction were explored. The co-design of 3D structure and material allows for a novel concept for further improving photothermal catalytic performance.
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页数:12
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