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Heterojunction of CuMn2O4/CeO2 nanocomposites for promoted photocatalytic H2 evolution under visible light
被引:30
作者:

Alzahrani, Khalid A.
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King Abdulaziz Univ, Fac Sci, Dept Chem, POB 80203, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Fac Sci, Dept Chem, POB 80203, Jeddah 21589, Saudi Arabia

Ismail, Adel A.
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King Abdulaziz Univ, Fac Sci, Dept Chem, POB 80203, Jeddah 21589, Saudi Arabia
Cent Met R&D Inst, Adv Mat Dept, CMRDI, POB 87, Cairo 11421, Egypt
Cent Met R&D Inst, CMRDI, POB 87, Cairo 11421, Egypt King Abdulaziz Univ, Fac Sci, Dept Chem, POB 80203, Jeddah 21589, Saudi Arabia

Alahmadi, Nadiyah
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机构:
Univ Jeddah, Coll Sci, Dept Chem, Jeddah, Saudi Arabia King Abdulaziz Univ, Fac Sci, Dept Chem, POB 80203, Jeddah 21589, Saudi Arabia
机构:
[1] King Abdulaziz Univ, Fac Sci, Dept Chem, POB 80203, Jeddah 21589, Saudi Arabia
[2] Cent Met R&D Inst, Adv Mat Dept, CMRDI, POB 87, Cairo 11421, Egypt
[3] Univ Jeddah, Coll Sci, Dept Chem, Jeddah, Saudi Arabia
[4] Cent Met R&D Inst, CMRDI, POB 87, Cairo 11421, Egypt
关键词:
Porous materials;
CeO2;
Heterojunctions;
H2;
Evolution;
Visible light;
MALACHITE GREEN-DYE;
HYDROGEN EVOLUTION;
IN-SITU;
NANOPARTICLES;
REDUCTION;
DEGRADATION;
CATALYSTS;
OXIDATION;
CO2;
MINERALIZATION;
D O I:
10.1016/j.jtice.2023.104692
中图分类号:
TQ [化学工业];
学科分类号:
0817 ;
摘要:
Background: It is significant to design a photocatalyst with highly efficient H-2 evolution utilizing solar energy to be a renewable energy sources.Method: Heterojunction CuMn2O4/CeO2 nanocomposites were constructed by a facile sol-gel approach utilizing a nonionic surfactant. The H2 evolution of the heterojunction CuMn2O4/CeO2 photocatalysts compared with pure CeO2 NPs was addressed under visible light. Glycerol was employed as an electron donor, and Pt NPs were in-situ photo-reduced during the reaction onto the CuMn2O4/CeO2 surface.Significant Findings: The TEM and XRD results verified the build of CuMn2O4/CeO2 nanocomposites with cubic phases of CeO2 and CuMn2O4 and particles size of about 10 nm. The results indicated that the H-2 evolution of 15%CuMn2O4/CeO2 photocatalyst was determined at about 23,650 mu mol.g(-1) after being illuminated for 9 h, while that of pure CeO2 was 4774 mu mol.g(-1). The H2 evolution rate of 15%CuMn2O4/CeO2 photocatalyst was enhanced five times larger than pure CeO2. The enhanced H2 evolution rate over the synthesized CuMn2O4/CeO2 nanocomposites can be attributed to the effective electron transport ability, enhancement of the separation ef-ficiency of electrons-hole. The construction of CuMn2O4/CeO2 S-scheme heterojunction is advantages to mini-mize the recombination of electron-hole, boosting the carriers lifetime, and enhancing the photocatalytic ability. The mechanism of photocatalytic H-2 evolution over CuMn2O4/CeO2 photocatalyst is illustrated. This study provides an effective and simple procedure to perform a reasonably constructed photocatalyst for cost-effective, stabilized and efficient solar H2 evolution applications.
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