TY - JOUR
T1 - Enhanced photocatalytic performance for CO2 reduction via an S-scheme heterojunction between perovskite nanocrystals and BiVO4
AU - Tsai, I. Hua
AU - Kuo, Yi Ru
AU - Hiramatsu, Hirotsugu
AU - Diau, Eric Wei Guang
N1 - Publisher Copyright:
© 2025 The Royal Society of Chemistry.
PY - 2025/1/20
Y1 - 2025/1/20
N2 - This study presents the successful synthesis of an S-scheme heterojunction between aged Cs0.5FA0.5PbBr3 (CF) perovskite nanocrystals and a BiVO4 semiconductor, aiming to enhance the photocatalytic CO2 reduction performance. Through meticulous optimization of synthetic methods, material ratios, and the pH of BiVO4, we achieved a remarkable CO production yield of 865 ± 38 μmol g−1 in 12 h when the CF to BiVO4 ratio was 15 : 1 and the pH value of the synthesized BiVO4 was adjusted to 4; the individual CF and BiVO4 photocatalysts can only produce CO with yields of 270 and 71 μmol g−1, respectively. Characterization techniques including XRD, SEM-EDS, PL, TCSPC, and UPS spectroscopy confirmed the formation of the S-scheme heterostructure and enhanced photocatalytic performance in varied proportions of CF versus BiVO4. The S-scheme heterojunction photocatalyst effectively inhibited electron-hole recombination, facilitating enhanced charge separation and electron-hole transfer for efficient photocatalytic CO2 reduction. This research not only rejuvenated the photocatalytic capabilities of aged perovskite materials but also addressed the critical challenge of formation of an S-scheme heterojunction between CF and BiVO4, offering a promising pathway for future design of efficient photocatalysts for CO2 reduction.
AB - This study presents the successful synthesis of an S-scheme heterojunction between aged Cs0.5FA0.5PbBr3 (CF) perovskite nanocrystals and a BiVO4 semiconductor, aiming to enhance the photocatalytic CO2 reduction performance. Through meticulous optimization of synthetic methods, material ratios, and the pH of BiVO4, we achieved a remarkable CO production yield of 865 ± 38 μmol g−1 in 12 h when the CF to BiVO4 ratio was 15 : 1 and the pH value of the synthesized BiVO4 was adjusted to 4; the individual CF and BiVO4 photocatalysts can only produce CO with yields of 270 and 71 μmol g−1, respectively. Characterization techniques including XRD, SEM-EDS, PL, TCSPC, and UPS spectroscopy confirmed the formation of the S-scheme heterostructure and enhanced photocatalytic performance in varied proportions of CF versus BiVO4. The S-scheme heterojunction photocatalyst effectively inhibited electron-hole recombination, facilitating enhanced charge separation and electron-hole transfer for efficient photocatalytic CO2 reduction. This research not only rejuvenated the photocatalytic capabilities of aged perovskite materials but also addressed the critical challenge of formation of an S-scheme heterojunction between CF and BiVO4, offering a promising pathway for future design of efficient photocatalysts for CO2 reduction.
UR - http://www.scopus.com/inward/record.url?scp=85216732991&partnerID=8YFLogxK
U2 - 10.1039/d4ta07216b
DO - 10.1039/d4ta07216b
M3 - Article
AN - SCOPUS:85216732991
SN - 2050-7488
VL - 13
SP - 6513
EP - 6523
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 9
ER -