In Situ ATR-IR Study on the Photocatalytic Decomposition of Amino Acids over Au/TiO2 and TiO2

被引:27
作者
Dolamic, Igor [1 ]
Buergi, Thomas [1 ,2 ]
机构
[1] Univ Neuchatel, Inst Phys, Lab Chim Phys Surfaces, CH-2009 Neuchatel, Switzerland
[2] Heidelberg Univ, Inst Phys Chem, D-69120 Heidelberg, Germany
关键词
SOLID-LIQUID INTERFACES; CO ADSORPTION; INFRARED-SPECTROSCOPY; GOLD NANOPARTICLES; AQUEOUS-SOLUTIONS; THIN-FILMS; OXIDATION; FTIR; DEGRADATION; DIOXIDE;
D O I
10.1021/jp1102753
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 photocatalytic degradation of L-asparagine and L-glutamic acid over Au/TiO2 and TiO2 catalysts was investigated in situ by attenuated total reflection infrared (ATR-IR) in combination with modulation excitation spectroscopy. Oxalate was detected on the catalyst surface, which has not been reported before for degradation of amino acids by studies focusing on intermediates in solution. The ATR-IR spectra provide valuable information on the fate of the nitrogen. Ammonium was detected, in agreement with previous studies, Most importantly, strong signals of cyanide were observed, and this assignment has been corroborated by N-15 labeling experiments. Cyanide was not reported before, to the best of our knowledge, for the photocatalytic degradation of amino acids. Cyanide was formed in the presence and the absence of gold particles on the TiO2 surface. The cyanide leads to leaching of gold via Au(CN)(2)(-) species that were detected in solution by mass spectrometry.
引用
收藏
页码:2228 / 2234
页数:7
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