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Boosting solar-light photocatalytic activity of Ni2 P-decorated ZnCr2O4 nanofibers for H2 evolution and tetracycline elimination
被引:1
|作者:
Peng, Hao
[1
]
Luo, Meiying
[2
]
Zheng, Xiaogang
[2
]
机构:
[1] Yangtze Normal Univ, Coll Chem & Chem Engn, Chongqing 408100, Peoples R China
[2] Neijiang Normal Univ, Coll Chem & Chem Engn, Neijiang 641100, Sichuan, Peoples R China
关键词:
ZnCr;
2;
O;
4;
nanofibers;
Solar light;
H;
evolution;
TCH elimination;
NANOSTRUCTURES;
NANOPARTICLES;
D O I:
10.1016/j.ceramint.2024.04.375
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:
Photocatalysis is a promising route to convert solar light into chemical energy for H2 evolution and pollutants degradation. Hence, Ni2P decorated ZnCr2O4 (Ni2P/ZnCr2O4) nanofibers were prepared for boosting solar-light induced water splitting and tetracycline hydrochloride (TCH) degradation. For comparison to ZnCr2O4 nanofibers, Ni2P/ZnCr2O4 composites exhibited the better photocatalytic activities for water splitting and TCH removal. Owing to the co-catalytic effect of Ni2P for the efficient photon capture, the charge carriers were rapidly separated and migrated at the interface between Ni2P and oxygen-defected ZnCr2O4. H2 evolution rate of optimal C-Ni2P/ZnCr2O4 with a nominal Ni2P content of 9.0 wt% was 575.89 mu mol g-1 h-1, and its apparent quantum yield at 420 nm was 15.25 %, while its H2 evolution decreased from 2815.13 to 2602.51 mu mol g-1 after fifth cycle. In addition, the removal efficiency of C-Ni2P/ZnCr2O4 was 93.68 % within 90 min, and declined to 88.76 % after five cycles for solar-light driven degradation of 50 mg L-1 TCH solution. The deactivation of C-Ni2P/ ZnCr2O4 was due to the photo-corrosion for the change in valence states of compositions.
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页码:26474 / 26481
页数:8
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