TY - JOUR
T1 - Microwave synthesized nano-photosensitizer of CdS QD/MoO3–OV/g–C3N4 heterojunction catalyst for hydrogen evolution under full-spectrum light
AU - Devarayapalli, K. C.
AU - Lee, Kiyoung
AU - Nam, Nguyen Dang
AU - Vattikuti, S. V.Prabhakar
AU - Shim, Jaesool
N1 - Publisher Copyright:
© 2020 Elsevier Ltd and Techna Group S.r.l.
PY - 2020/12/15
Y1 - 2020/12/15
N2 - 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 (H2) production rate with the CdS QDs-anchored MoO3/g-C3N4 heterostructure photocatalysts reached 294.32 μmol 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.
AB - 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 (H2) production rate with the CdS QDs-anchored MoO3/g-C3N4 heterostructure photocatalysts reached 294.32 μmol 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.
KW - CdS QDs
KW - Layered material
KW - Visible photocatalyst
KW - Water splitting
UR - http://www.scopus.com/inward/record.url?scp=85090482028&partnerID=8YFLogxK
U2 - 10.1016/j.ceramint.2020.08.004
DO - 10.1016/j.ceramint.2020.08.004
M3 - Article
AN - SCOPUS:85090482028
SN - 0272-8842
VL - 46
SP - 28467
EP - 28480
JO - Ceramics International
JF - Ceramics International
IS - 18
ER -