个人信息
教师姓名：尹良君
教师拼音名称：yinliangjun
电子邮箱：ljyin@uestc.edu.cn
所在单位：电子科学与工程学院
学历：博士研究生毕业
办公地点：国家电磁辐射控制材料工程技术研究中心 C318B
性别：男
学位：工学博士学位
职称：教授
在职信息：在职人员
毕业院校：中国科技大学
硕士生导师
曾获荣誉：省部级人才计划
-
所属院系： 电子科学与工程学院（示范性微电子学院）
-
学科：电子信息材料与元器件
其他联系方式
通讯/办公地址：
移动电话：
邮箱：
论文成果
Self-Supported Ceramic Electrode of 1T-2H MoS<sub>2</sub> Grown on the TiC Membrane for Hydrogen Production
发布时间：2025-05-23 点击次数：
所属单位：[1]Univ Sci & Technol China, Dept Mat Sci & Engn, CAS Key Lab Mat Energy Convers, Hefei 230026, Anhui, Peoples R China;[2]PetroChina, New Energy Res Ctr, Res Inst Petr Explorat & Dev RIPED, Beijing 100083, Peoples R China;[3]Univ Elect Sci & Technol China, Sch Energy Sci & Engn, Chengdu 611731, Peoples R China;[4]Univ Ioannina, Dept Mat Sci & Engn, GR-45110 Ioannina, Greece;[5]Univ Sci & Technol China, Dept Modern Mech, CAS Key Lab Mech Behav & Design Mat, Hefei 230026, Anhui, Peoples R China
发表刊物：CHEMISTRY OF MATERIALS
摘要：Binder-free, cost-effective, and stable hydrogen evolution reaction electrocatalytic electrodes with a customized size are urgently needed for large-scale industrial hydrogen production. Toward this challenge, self-supported TiC@MoS2 (TCMS) ceramic membrane electrodes were fabricated by a self-template strategy. Porous TiC ceramic membranes with straight finger-like pores were first fabricated by phase inversion tape-casting and sintering. Then, a 1T-2H MoS2 nanosheet layer grew on the porous conductive TiC skeleton. The high conductivity of the TCMS skeleton promotes charge transfer, while the porous structure, which consists of abundant finger-like and cavernous pores, favors proton transfer and bubble transfer during the electrolysis process. The optimal TCMS composition displayed an overpotential of -127 mV at -10 mA.cm(-2), a Tafel slope of 41 mV.dec(-1), and an extremely high electrochemical active area of 1079.4 mF.cm(-2) as well as remarkable stability in 0.5 M H2SO4. A high Faradaic efficiency of 99.7% was also achieved. The superior electrocatalytic performance was ascribed to the synergistic effect of the tight bonding and the crystal matching between TiC and MoS2, the unique dual pore structure, the abundant exposed active sites of MoS2 nanoflakes, and the high 1T-MoS2 content. First-principles density functional calculations showed that the 1T-MoS2/TiC hybrid has the lowest free energy for H adsorption (0.116 eV) and the highest density of states near the Fermi level, which leads to a strong catalytic activity.
文献类型：Article
卷号：33
期号：15
页面范围：6217-6226
ISSN号：0897-4756
是否译文：否
