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.
引用
收藏
页码:26474 / 26481
页数:8
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