TY - JOUR
T1 - Design of S-scheme CdS/La2O3 heterojunction for excellent photocatalytic H2 evolution performance under simulated sunlight irradiation
AU - Ahmad, Irshad
AU - Alfaifi, Mohammed Qasem
AU - Alassmy, Yasser A.
AU - Abduljawad, Marwan M.
AU - Khasawneh, Mohammad Ahmad
AU - Ali, Muhammad Danish
AU - Karim, Md Rezaul
AU - Ashraf, I. M.
N1 - Publisher Copyright:
© 2024 Hydrogen Energy Publications LLC
PY - 2025/1/13
Y1 - 2025/1/13
N2 - Constructing S-scheme heterojunction photocatalysts with promising H2 evolution performance remains challenging. Herein, a series of S-scheme CdS/La2O3 heterojunctions is designed and prepared through a microwave-assisted hydrothermal process to explore photocatalytic H2 evolution from water-glycerol mixture. The optimized CdS/La2O3 photocatalyst demonstrates an excellent H2 evolution rate of 18.50 mmolg−1h−1 from water-glycerol mixture under simulated sunlight irradiation, exhibiting a 14.5-fold and 26.8-fold enhancement compared to pure CdS (1.28 mmolg−1h−1) and La2O3 (0.69 mmolg−1h−1), respectively. The improved performance is primarily assigned to the S-scheme heterojunction formed between La2O3 and CdS, which promotes the separation and migration of photoinduced electron-hole pairs. Additionally, the optimized CdS/La2O3 photocatalyst manifests strong stability, exhibiting no significant performance loss in the H2 evolution rate over 20 h of recycling experiments. This work facilitates valuable insights for constructing high-performance and stable S-scheme photocatalysts for H2 evolution.
AB - Constructing S-scheme heterojunction photocatalysts with promising H2 evolution performance remains challenging. Herein, a series of S-scheme CdS/La2O3 heterojunctions is designed and prepared through a microwave-assisted hydrothermal process to explore photocatalytic H2 evolution from water-glycerol mixture. The optimized CdS/La2O3 photocatalyst demonstrates an excellent H2 evolution rate of 18.50 mmolg−1h−1 from water-glycerol mixture under simulated sunlight irradiation, exhibiting a 14.5-fold and 26.8-fold enhancement compared to pure CdS (1.28 mmolg−1h−1) and La2O3 (0.69 mmolg−1h−1), respectively. The improved performance is primarily assigned to the S-scheme heterojunction formed between La2O3 and CdS, which promotes the separation and migration of photoinduced electron-hole pairs. Additionally, the optimized CdS/La2O3 photocatalyst manifests strong stability, exhibiting no significant performance loss in the H2 evolution rate over 20 h of recycling experiments. This work facilitates valuable insights for constructing high-performance and stable S-scheme photocatalysts for H2 evolution.
KW - CdS
KW - H evolution
KW - In-situ XPS
KW - LaO
KW - Photocatalyst
KW - S-scheme heterojunction
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U2 - 10.1016/j.ijhydene.2024.12.144
DO - 10.1016/j.ijhydene.2024.12.144
M3 - Article
AN - SCOPUS:85211701418
SN - 0360-3199
VL - 98
SP - 1052
EP - 1066
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
ER -