The enhanced piezoelectric field induced by self-polarization promotes hydrogen evolution reaction on g-C3N4/MoO3/PVDF-TrFE membrane under low-speed water flow

被引:0
作者
Zhu, Yanbing [1 ]
Xiu, Hao [1 ]
Xue, Gang [1 ]
Lei, Tianyong [1 ]
Wang, Yu [1 ]
Li, Zhongfang [1 ]
Cong, Shuren [2 ]
Wei, Tingting [1 ]
机构
[1] Kunming Univ Sci & Technol, Fac Sci, Dept Phys, Kunming 650093, Peoples R China
[2] Kunming Inst Phys, Infrared Detector Ctr, Kunming 650000, Yunnan, Peoples R China
关键词
Piezo-photocatalytic membrane; Self-polarization; beta-Phase enhancement; Hydrogen evolution reaction; HETEROJUNCTION; PVDF;
D O I
10.1016/j.apsusc.2025.162452
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
The piezoelectric properties are closely related to the properties of photocatalytic membrane in water environment. Here, a self-polarized g-C3N4/MoO3/PVDF-TrFE membrane with high piezoelectricity was synthesized using a facile spin-coating strategy. In the presence of a low-speed water flow, a stabilized photocatalytic hydrogen evolution rate (538.8 mu mol g-1h- 1 ) was obtained for the g-C3N4/MoO3/PVDF-TrFE membrane. Experimental results revealed that the g-C3N4/MoO3 induced a reorganization of PVDF-TrFE structure and thereby enlarged the polarization electric field to promote the directional migration of charge carriers and exciton dissociation. Additionally, pressure current test demonstrated that under the same pressure conditions, gC3N4/MoO3/PVDF-TrFE exhibited a higher response than PVDF-TrFE. This work establishes a new method for the polarization electric field and provides a deeper understanding of the hydrogen evolution mechanism.
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页数:9
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