个人信息Personal Information
教授
博士生导师
硕士生导师
任职 : 大连理工大学成都研究院院长
性别:男
毕业院校:中科院大连化学物理研究所
学位:博士
所在单位:化工学院
学科:化学工艺. 物理化学. 功能材料化学与化工
办公地点:大连理工大学西部校区化工综合楼A401室
联系方式:辽宁省大连市高新区凌工路2号,邮编116024
电子邮箱:changhai@dlut.edu.cn
PdAg/CNT catalyzed alcohol oxidation reaction for high-performance anion exchange membrane direct alcohol fuel cell (alcohol = methanol, ethanol, ethylene glycol and glycerol)
点击次数:
论文类型:期刊论文
发表时间:2016-12-15
发表刊物:APPLIED CATALYSIS B-ENVIRONMENTAL
收录刊物:SCIE、EI、Scopus
卷号:199
页面范围:494-503
ISSN号:0926-3373
关键字:Alcohol oxidation reaction; Aldehyde oxidation reaction; Direct alcohol fuel cell; Carbon carbon bond cleavage; Electrocatalyst
摘要:PdAg supported on carbon nanotubes (PdAg/CNT) with an average particle size of 2.7 nm is prepared by an aqueous phase reduction method for alcohol oxidation reaction in direct alcohol fuel cells. In a half-cell system with three electrodes, the peak mass activity of PdAg/CNT reaches 0.105 mA mu g(pd)(-1), 0.305 mA mu g(pd)(-1), 2.105 mA mu g(Pd)(-1), and 8.53 mA mu g(Pd)(-1) for methanol oxidation reaction, ethanol oxidation reaction, ethylene glycol oxidation reaction, and glycerol oxidation reaction, respectively, in 1 M KOH 0.1 M alcohol electrolyte. These values are higher than the mass activity of Pd/CNT at the same applied potential. With PdAg/CNT (0.5 mg(PdperMEA)(-1)) as an anode catalyst, a direct methanol fuel cell, a direct ethanol fuel cell, a direct ethylene glycol fuel cell and a direct glycerol fuel cell-achieve peak power densities of 135.1 mW cm(-2), 202.3 mW cm(-2), 245.2 mW cm(-2), and 276.2 mW cm(-2), with corresponding peak-mass activities of 270.2 mW mg(PdperMEA)(-1), 404.6 mW mg(PdperMEA)(-1), 490.4 mW mg(PdperMEA)(-1), and 552.4 mW mg(PdperMEA)(-1), respectively, at 80 degrees C and ambient pressure. Ag has shown excellent activity towards aldehyde (formaldehyde, acetaldehyde, and glyoxylate) oxidation, thus, the enhancement in alcohol oxidation on PdAg/CNT is proposed due to Ag's promotion of intermediate aldehyde oxidation. PdAg/CNT also improves the fuel efficiency of glycerol oxidation by contributing to the C-C bond cleavage of C-3 glycerol to C-2 oxalate. (C) 2016 Elsevier B.V. All rights reserved.