The functionalisation of graphite surfaces with nitric acid: Identification of functional groups and their effects on gold deposition

被引:61
|
作者
Burgess, Rebecca [1 ]
Buono, Carlo [1 ]
Davies, Philip. R. [1 ]
Davies, Robert J. [2 ]
Legge, Thomas [1 ]
Lai, Amy [1 ]
Lewis, Ryan [1 ]
Morgan, David J. [1 ]
Robinson, Neil [1 ]
Willock, David J. [1 ]
机构
[1] Cardiff Univ, Sch Chem, Cardiff Catalysis Inst, Cardiff CF10 3AT, S Glam, Wales
[2] Univ London Imperial Coll Sci Technol & Med, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会;
关键词
Gold; Carbon; Graphite; Catalysis; AFM; XPS; Hydroxyl groups; Nucleation; INITIO MOLECULAR-DYNAMICS; TOTAL-ENERGY CALCULATIONS; CHEMICAL DERIVATIZATION; CARBON; HYDROCHLORINATION; QUANTIFICATION; TOPOGRAPHY; TRANSITION; CATALYSTS; METALS;
D O I
10.1016/j.jcat.2014.12.021
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The role of surface oxygen species in the nucleation and reactions of metal nanoparticles on carbon surfaces has been explored using model systems based on graphite supported with DFT calculations. Features in the X-ray photoelectron spectra at characteristic binding energies of 532.6 eV, 531.8 eV, and 533.5 eV were unambiguously assigned to hydroxyl, ketone, and ether groups after selective derivatization. Surfaces treated with nitric acid generate almost exclusively hydroxide groups which on heating to 573 K transform into ketones and ethers. Gold nanoparticles deposited from an aurochloric acid solution show a better dispersion on the hydroxylated surface than on either the clean or the ketone-covered surface and whereas on the hydroxylated surface the adsorbed gold was reduced completely to Au-0, a small component attributed to Au3+ was present after deposition at the ketone-/ether-covered surface. DFT calculations confirm that gold atoms adsorb more strongly to a hydroxylated step edge than one functionalised with ketone groups. The results give an insight into the effects of the acid washing of carbon catalysts before loading with the active metal components. (C) 2014 The Authors. Published by Elsevier Inc.
引用
收藏
页码:10 / 18
页数:9
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