梁长海

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

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PdAg/CNT catalyzed alcohol oxidation reaction for high-performance anion exchange membrane direct alcohol fuel cell (alcohol = methanol, ethanol, ethylene glycol and glycerol)

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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.