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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.
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页码:28467 / 28480
页数:14
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