Microwave synthesized nano-photosensitizer of CdS QD/MoO3-OV/g-C3N4 heterojunction catalyst for hydrogen evolution under full-spectrum light

被引:35
作者
Devarayapalli, K. C. [1 ]
Lee, Kiyoung [2 ,3 ]
Nguyen Dang Nam [4 ,5 ]
Vattikuti, S. V. Prabhakar [1 ]
Shim, Jaesool [1 ]
机构
[1] Yeungnam Univ, Sch Mech Engn, Gyongsan 38541, South Korea
[2] Kyungpook Natl Univ, Sch Nano & Mat Sci & Engn, 2559 Gyeongsang Daero, Sangju, Gyeongbuk, South Korea
[3] Kyungpook Natl Univ, Dept Adv Sci & Technol Convergence, 2559 Gyeongsang Daero, Sangju 37224, South Korea
[4] Duy Tan Univ, Inst Fundamental & Appl Sci, Future Mat & Devices Lab, Ho Chi Minh City 700000, Vietnam
[5] Duy Tan Univ, Fac Environm & Chem Engn, Da Nang 550000, Vietnam
基金
新加坡国家研究基金会;
关键词
CdS QDs; Visible photocatalyst; Layered material; Water splitting; HIGH PHOTOCATALYTIC PERFORMANCE; G-C3N4; NANOSHEETS; FACILE SYNTHESIS; H-2; EVOLUTION; METHYL-ORANGE; DOPED G-C3N4; EFFICIENT; WATER; GENERATION; DEGRADATION;
D O I
10.1016/j.ceramint.2020.08.004
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this study, facile solid-state CdS quantum dots (QDs) supported MoO3/g-C3N4 nanostructure photocatalysts were prepared via an innovative in-situ deposition protocol with consecutive ionic layer adsorption and reaction. The CdS QDs-anchored MoO3/g-C3N4 heterostructure photocatalysts demonstrated enhanced visible-light absorption capacity, which was realized by the quantum confinement of the CdS QDs. The maximum photocatalytic hydrogen (H-2) production rate with the CdS QDs-anchored MoO3/g-C3N4 heterostructure photocatalysts reached 294.32 mu mol g(-1).h(-1), which was 76.84, 215.21, 27.12, and 3.64 folds superior as compare to bare g-C3N4, MoO3, CdS, and MoO3/g-C3N4 catalysts, respectively. The enriched photocatalytic performance was mainly credited to the high surface area and MoO3 with oxygen vacancies (OV), ultra-thin g-C3N4 and high optical adsorption ability of CdS QDs. Thus, forming a dual Z-scheme system in the CdS QDs-supported MoO3-OV/g-C3N4 nanostructures not only facilitated efficient interfacial charge transfer but also preserved the robust redox ability of the photoinduced electrons and holes.
引用
收藏
页码:28467 / 28480
页数:14
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