期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 134, 期 11, 页码 5014-5017出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja2108933
关键词
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资金
- National Science Foundation [CHE-0848883]
- Department of Energy through the Conn Center for Renewable Energy Research [EE-00003206]
Here we describe the oxidation of <4 nm diameter Au nanoparticles (NPs) attached to indium tin oxide-coated glass electrodes in Br- and Cl- solution. Borohydride reduction of AuCl4- in the presence of hexanethiol or trisodium citrate (15 min) led to Au NPs <4 nm in diameter. After electrochemical and ozone removal of the hexanthiolate ligands from the thiol-coated Au NPs, Au oxidation peaks appeared in the range 0-400 mV vs Ag/AgCl (1 M KCl), which is 850-450 mV negative of the bulk Au oxidation peak near 850 mV. The oxidation potential of citrate-coated Au NPs is in the 300-500 mV range and those of 4 and 12 nm diameter Au NPs in the 660-780 mV range. The large negative shift in potential agrees with theory for NPs in the 1-2 nm diameter range. The oxidation potential of Au in Cl- solution is positive of that in Br- solution, but the difference decreases dramatically as the NP size decreases, showing less dependence on the halide for smaller NPs.
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