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author:

Wang, J.-Y. (Wang, J.-Y..) [1] | Peng, B. (Peng, B..) [2] | Xie, H.-N. (Xie, H.-N..) [3] | Cai, W.-B. (Cai, W.-B..) [4]

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Scopus

Abstract:

In situ ATR-FTIR spectroscopy has been extended to the study of CO and pyridine adsorptions at crystalline and amorphous Ni-P alloy film electrodes, with an emphasis on the alloying effect of P on their adsorption configurations on Ni sites. The Ni-P films were prepared with initial seeding of a catalytic Pd layer on Si, followed by chemical deposition. Transition from bridge-bonded CO (COB) dominant to linearly bonded CO (COL) dominant adsorption was found with increasing P content, together with a blue-shift in the COL vibrational frequency and an attenuation of the Stark tuning rate of COL. As for Py on Ni-P electrodes, essentially the N-end-on adsorption was revealed, in contrast to the edge-tilted adsorption on Ni electrode. Modification in the adsorption configurations as compared to that on Ni electrode is ascribed mainly to the site-blocking effect with alloying P, rather than to partial electron transfer between Ni and P. © 2008 Elsevier Ltd. All rights reserved.

Keyword:

Adsorption; ATR-FTIR spectroscopy; CO; Ni-P alloy electrode; Pyridine

Community:

  • [ 1 ] [Wang, J.-Y.]Shanghai Key Laboratory for Molecular Catalysis and Innovative Materials, Department of Chemistry, Fudan University, Shanghai, 200433, China
  • [ 2 ] [Peng, B.]Shanghai Key Laboratory for Molecular Catalysis and Innovative Materials, Department of Chemistry, Fudan University, Shanghai, 200433, China
  • [ 3 ] [Xie, H.-N.]The College of Chemistry and Chemistry Engineering, Fuzhou University, Fuzhou, 350108, China
  • [ 4 ] [Cai, W.-B.]Shanghai Key Laboratory for Molecular Catalysis and Innovative Materials, Department of Chemistry, Fudan University, Shanghai, 200433, China

Reprint 's Address:

  • [Cai, W.-B.]Shanghai Key Laboratory for Molecular Catalysis and Innovative Materials, Department of Chemistry, Fudan University, Shanghai, 200433, China

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Source :

Electrochimica Acta

ISSN: 0013-4686

Year: 2009

Issue: 6

Volume: 54

Page: 1834-1841

3 . 3 2 5

JCR@2009

5 . 5 0 0

JCR@2023

JCR Journal Grade:1

CAS Journal Grade:1

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

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