In-situ growth of g-C3N4 nanosheets on Nb2O5 nanofibers for enhanced performance in photocatalysis and lithium-sulfur battery

被引:6
作者
Liu, Haiyang [1 ]
Li, Xinyue [1 ]
Ma, Lumin [1 ]
Sun, Feng [1 ]
Yue, Bin [1 ]
Ma, Qianli [1 ]
Wang, Jinxian [1 ]
Liu, Guixia [1 ]
Yu, Hui [1 ]
Yu, Wensheng [1 ,2 ]
Dong, Xiangting [1 ]
Su, Zhongmin [2 ,3 ]
机构
[1] Changchun Univ Sci & Technol, Key Lab Appl Chem & Nanotechnol Univ Jilin Prov, Changchun 130022, Peoples R China
[2] Changchun Univ Sci & Technol, Sch Chem & Environm Engn, Changchun 130012, Peoples R China
[3] Jilin Univ, Inst Theoret Chem, Coll Chem, State Key Lab Supramol Struct & Mat, Changchun 130021, Peoples R China
关键词
Electrospinning; Double crucibles gas-solid reaction; Photocatalysis; Li-S battery; II HETEROJUNCTIONS; CHARGE SEPARATION; H-2; EVOLUTION; HETEROSTRUCTURES; DEGRADATION; NITRIDE; NANOPARTICLES; MICROSPHERES; POLLUTANTS; GRAPHENE;
D O I
10.1016/j.colsurfa.2023.131572
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A Nb2O5/g-C3N4 composite with a controllable loading amount of g-C3N4 nanosheets is successfully prepared by a combination of electrospinning and the double crucible gas-solid reaction method. During the heat treatment process, the precursor molecules of melamine gas are in-situ polymerized on the surface of Nb2O5 nanofibers to form g-C3N4 nanosheets. The Nb2O5 nanofibers ultralong one-dimensional nanostructure can effectively avoid the aggregations of g-C3N4 and form tight heterojunction interfaces. The optimized Nb2O5/g-C3N4 composite material improved the photocatalytic activity for methylene blue degradation, with a rate constant twice that of Nb2O5 nanofibers and 3.8 times that of pure g-C3N4. Using the combination of DFT theoretical calculations and capture experiments, the transfer mechanism of the Nb2O5/g-C3N4 type-II heterojunction is confirmed. It was found that the d orbital of Nb and the p orbital of N were the main active site of the photocatalytic reaction. Meanwhile, the lithium-sulfur (Li-S) battery assembled with NOCN-8 as the host material exhibited a high initial discharge capacity of 900 mAh g-1 at 0.5 C, and its capacity decay rate was less than 0.1% after 500 cycles. It shows that NOCN-8 can effectively adsorb polysulfide and catalyze the conversion reaction of polysulfide. This work provides a novel route for the synthesis of the Nb2O5/g-C3N4 composite, and has great potential in the development of environmental remediation and energy applications.
引用
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页数:12
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