A convenient double defect engineering avenue for NH2-MIL-125 to enhance photocatalytic hydrogen evolution and NO removal via accelerating the electron mobility

被引:0
|
作者
Liu, Xingyan [1 ]
Xiong, Tianrong [1 ]
Xu, Yonggang [1 ]
Yang, Kunhe [1 ]
He, Youzhou [1 ]
Yang, Haifeng [1 ]
Wu, Hong [1 ]
Jing, Jiajia [1 ]
Li, Siqi [3 ]
Wei, Siping [2 ]
机构
[1] Chongqing Technol & Business Univ, Coll Environm & Resources, Chongqing Key Lab Catalysis & New Environm Mat, Chongqing 400067, Peoples R China
[2] Southwest Med Univ, Sch Pharm, Dept Med Chem, Cent Nervous Syst Drug Key Lab Sichuan Prov, Luzhou 646000, Peoples R China
[3] Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
NH2-MIL-125(Ti); Photocatalysis; Double defect engineering avenue; Hydrogen evolution; NO removal; POLLUTANTS;
D O I
10.1016/j.fuel.2024.133860
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Defect engineering for MOFs is a promising approach to accelerate the charge transfer to further enhance the photocatalytic performance. Up to now, the current defect engineering strategy for MOFs mainly focuses on a single adjustment mode with the apparent ceiling effect, whether the further break out of the ceiling effect could be achieved through the combination of two or more adjustment modes is still in its infancy. In this work, the original NH2-MIL-125 was firstly adjusted by a single adjustment mode in ethanol solvothermal method to obtain partially linker defective NM-125-X (where X signifies the distinct temperatures used in the solvothermal treatment, with optimal results observed at X =120). Subsequently, the NM-125-120 was further re-regulated by adjusting the ligand defects through another adjustment mode in water heating agitation, resulting in the ultimate defective NM-125-120-65. The NM-125-120-65 obtained through double defect engineering avenue showed superior photocatalytic performance with the hydrogen production rate of 11585.23 mu mol center dot g- 1 , which was 1.23 and 14.05 times as those of partially defective NM-125-120 (9427.65 mu mol center dot g-1) and original NH2-MIL- 125 (824.85 mu mol center dot g-1), respectively. In addition, the NO removal rate of NM-125-120-65 was 64.8 % also higher than that of NM-125-120 (37.8 %) and NH2-MIL-125 (23.6 %). Through a series of comparative experiments, especially TGA and XPS, it was noted that the ligand defective NH2-MIL-125 can be formed by ethanol solvothermal method, and it was also confirmed that through further re-regulating the ligand defects in water heating agitation, the linker defects could also be further expanded. The PL emission spectra, IT diagrams, and EIS measurements displayed that the NM-125-120-65 had outstanding conductivity and excellent electron mobility compared to NM-125-120 and NH2-MIL-125. This work provided a novel approach for the subsequent defect engineering by another adjustment mode based on the existing defective MOFs via double linker defect engineering adjustment modes, so as to further obtain better photocatalytic performance for solving the environmental and energy crisis.
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页数:11
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