个人信息Personal Information
教授
博士生导师
硕士生导师
性别:男
毕业院校:中国科学院兰州化学物理研究所
学位:博士
所在单位:环境学院
办公地点:环境楼 B415
联系方式:Tel: 0411-84706658
电子邮箱:xyli@dlut.edu.cn
Photo-driven bioelectrochemical photocathode with polydopamine-coated TiO2 nanotubes for self-sustaining MoS2 synthesis to facilitate hydrogen evolution
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论文类型:期刊论文
发表时间:2019-02-15
发表刊物:JOURNAL OF POWER SOURCES
收录刊物:SCIE
卷号:413
页面范围:310-317
ISSN号:0378-7753
关键字:MoS2 nanosheets; Electron transfer; Photo-bioelectrochemical system; Double-electron donor; HER
摘要:Developing low-energy and high-efficiency photoelectrocatalysts towards hydrogen evolution reaction is one of the frontier technologies capturing intensive research enthusiasm. In this work, a sustainable solar-driven microbial fuel cell is successfully constructed to synthesize rich edge sites of MoS2 nanomaterials and in situ utilize dual electrons mode for hydrogen generation under visible light illumination (> 420 nm). For this photo-driven coupling system, the continuous formation of MoS2 catalyst is more beneficial for efficient hydrogen generation without external bias assistance. Such unique preparation method endows the system to possess more active edge sites for MoS2 exposure, and promotes the obtained materials to exhibit super-hydrophilic behavior. Additionally, the introduction of MoS2 semiconductor could cooperate with bio-electrons to dramatically hinder the recombination of photo-excited electron-hole pairs, leaving more opportunities for photo-electrons to participate hydrogen evolution reaction under the bioelectric field. Simultaneously, the constructed MoS2 based electrode performs excellent photoelectrochemical performance (the onset overpotential only similar to 36 mV vs. SHE, Tafel slope of 53 mV per decade) and hydrogen evolution activities for hydrogen production with 0.003 m(3)m(-3) min(-1) rate. This work not only leads to a promising approach for the preparation of high efficient photoelectrocatalysts, but also highlights the potential strategy for diverse applications.