Interaction of CO with hydrous ruthenium oxide and development of a chemoresistive ambient CO sensor

被引:47
作者
Adeyemo, Adedunni [1 ]
Hunter, Gary [2 ]
Dutta, Prabir K. [1 ]
机构
[1] Ohio State Univ, Dept Chem, Columbus, OH 43210 USA
[2] NASA, Glenn Res Ctr, Cleveland, OH 44135 USA
关键词
Infrared spectroscopy; Room temperature gas sensor; CO oxidation; X-ray photoelectron spectroscopy; Metal oxide sensor; Hydrated ruthenium oxide; CARBON-MONOXIDE; ELECTROCHEMICAL CAPACITORS; ELECTRICAL-PROPERTIES; DRIFT SPECTROSCOPY; CHARGE STORAGE; TAP REACTOR; THIN-FILMS; OXIDATION; RUO2; DIOXIDE;
D O I
10.1016/j.snb.2010.12.027
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Hydrated ruthenium oxide (RuOx(OH)(y)), the material of interest in this study was prepared by reaction of an aqueous solution of ruthenium chloride with base. This material was amorphous, made up of 20-50 nm particles and contains Ru(III) and Ru(IV), as determined by X-ray photoelectron spectroscopy. The conductivity of thick films of RuOx(OH)(y) decreased in the presence of CO in a background of air and this change was reversible. Infrared spectroscopy showed the formation of carbonates in the presence of CO, which disappeared upon replacement of CO with O-2. Upon heating RuOx(OH)(y), there was a gradual conversion to crystalline RuO2 beyond 200 degrees C. With these heated materials, the resistance change in the presence of CO at room temperature also gradually diminished. We propose that oxidation of CO on RuOx(OH)(y) leads to reduction of the ruthenium and a decrease in conductivity. With the conversion to crystalline RuO2 upon heating, the material becomes metallic and conductivity changes are diminished. The change in conductivity of RuOx(OH)(y) with CO provides a convenient platform for an ambient CO sensor. Such a device also does not show interference from hydrocarbons (2000 ppm), ammonia (150 ppm), CO2 (2000 ppm), NO (15 ppm) and NO2 (15 ppm). (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:307 / 315
页数:9
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