Methanol electrooxidation on core-shell Ag@Pdx catalysts

The performance of a direct methanol fuel cell (DMFC) is strongly dependent on the catalytic anode. A high-performance anode is expected to offer enhanced intrinsic activity and/or a large electrochemical surface area. Herein, a series of Ag-core/Pd-shell (Ag@Pdx, x = 1,3,5) catalysts are synthesize...

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Main Authors: Xiaobo Yang, Xili Tong, Xingchen Liu, Kaixi Li, Nianjun Yang
Format: Article
Language:English
Published: Elsevier 2021-02-01
Series:Electrochemistry Communications
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1388248121000011
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spelling doaj-c74e2c859f1f44e39c9a1f8f25b9f9842021-03-01T04:14:36ZengElsevierElectrochemistry Communications1388-24812021-02-01123106917Methanol electrooxidation on core-shell Ag@Pdx catalystsXiaobo Yang0Xili Tong1Xingchen Liu2Kaixi Li3Nianjun Yang4State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China; Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing 100049, ChinaState Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China; Corresponding authors.State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, ChinaState Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, ChinaInstitute of Materials Engineering, University of Siegen, Siegen 57076, Germany; Corresponding authors.The performance of a direct methanol fuel cell (DMFC) is strongly dependent on the catalytic anode. A high-performance anode is expected to offer enhanced intrinsic activity and/or a large electrochemical surface area. Herein, a series of Ag-core/Pd-shell (Ag@Pdx, x = 1,3,5) catalysts are synthesized in which the thickness of the Pd shell is varied. Both tensional strain and electron transfer between the Ag core and the Pd shell are found to affect the intrinsic activity of these Ag@Pdx catalysts. Of these, the Ag@Pd3 catalyst exhibits the best performance for the methanol oxidation reaction (MOR), showing 4.1 times higher mass activity and 2.6 times higher specific activity than a Pd/C catalyst. Furthermore, density functional theory calculations show that this high MOR performance stems from a stronger adsorption of CH3OH and OH on the Pd active sites. This catalyst is thus a promising candidate for inclusion in a high-performance DMFC.http://www.sciencedirect.com/science/article/pii/S1388248121000011Methanol oxidation reactionPd electrocatalystCore-shell structureStrain effect
collection DOAJ
language English
format Article
sources DOAJ
author Xiaobo Yang
Xili Tong
Xingchen Liu
Kaixi Li
Nianjun Yang
spellingShingle Xiaobo Yang
Xili Tong
Xingchen Liu
Kaixi Li
Nianjun Yang
Methanol electrooxidation on core-shell Ag@Pdx catalysts
Electrochemistry Communications
Methanol oxidation reaction
Pd electrocatalyst
Core-shell structure
Strain effect
author_facet Xiaobo Yang
Xili Tong
Xingchen Liu
Kaixi Li
Nianjun Yang
author_sort Xiaobo Yang
title Methanol electrooxidation on core-shell Ag@Pdx catalysts
title_short Methanol electrooxidation on core-shell Ag@Pdx catalysts
title_full Methanol electrooxidation on core-shell Ag@Pdx catalysts
title_fullStr Methanol electrooxidation on core-shell Ag@Pdx catalysts
title_full_unstemmed Methanol electrooxidation on core-shell Ag@Pdx catalysts
title_sort methanol electrooxidation on core-shell ag@pdx catalysts
publisher Elsevier
series Electrochemistry Communications
issn 1388-2481
publishDate 2021-02-01
description The performance of a direct methanol fuel cell (DMFC) is strongly dependent on the catalytic anode. A high-performance anode is expected to offer enhanced intrinsic activity and/or a large electrochemical surface area. Herein, a series of Ag-core/Pd-shell (Ag@Pdx, x = 1,3,5) catalysts are synthesized in which the thickness of the Pd shell is varied. Both tensional strain and electron transfer between the Ag core and the Pd shell are found to affect the intrinsic activity of these Ag@Pdx catalysts. Of these, the Ag@Pd3 catalyst exhibits the best performance for the methanol oxidation reaction (MOR), showing 4.1 times higher mass activity and 2.6 times higher specific activity than a Pd/C catalyst. Furthermore, density functional theory calculations show that this high MOR performance stems from a stronger adsorption of CH3OH and OH on the Pd active sites. This catalyst is thus a promising candidate for inclusion in a high-performance DMFC.
topic Methanol oxidation reaction
Pd electrocatalyst
Core-shell structure
Strain effect
url http://www.sciencedirect.com/science/article/pii/S1388248121000011
work_keys_str_mv AT xiaoboyang methanolelectrooxidationoncoreshellagpdxcatalysts
AT xilitong methanolelectrooxidationoncoreshellagpdxcatalysts
AT xingchenliu methanolelectrooxidationoncoreshellagpdxcatalysts
AT kaixili methanolelectrooxidationoncoreshellagpdxcatalysts
AT nianjunyang methanolelectrooxidationoncoreshellagpdxcatalysts
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