Abstract
A study of the photocatalytic behaviour of silver modified titanium dioxide materials for the decomposition and reduction of nitric oxide (NO) gas has been carried out. The effects of silver loading, calcination temperature, and reaction conditions have been investigated. Prepared photocatalysts were characterised using XRD, TEM, and XPS. A continuous flow reactor was used to determine the photocatalytic activity and selectivity of NO decomposition in the absence of oxygen as well as NO reduction using CO as the reducing agent, over the prepared photocatalysts. XRD and TEM analysis of the photocatalysts showed that crystalline silver nitrate particles were present on the titanium dioxide surface after calcination at temperatures of up to200∘C. The silver nitrate particles are thermally decomposed to form metallic silver clusters at higher temperatures. XPS analysis of the photocatalysts showed that for each of the temperatures used, bothAg+andAg0were present and that theAg0/Ag+ratio increased with increasing calcination temperature. The presence of metallic silver species on theTiO2surface dramatically increased the selectivity forN2formation of both decomposition and reduction reactions. When CO was present in the reaction gas, selectivities of over 90%were observed for all the Ag-TiO2photocatalysts that had been calcined at temperatures above200∘C. Unfortunately these high selectivities were at the expense of photocatalytic activity, with lower NO conversion rates than those achieved over unmodifiedTiO2photocatalysts.
Subject
General Materials Science,Renewable Energy, Sustainability and the Environment,Atomic and Molecular Physics, and Optics,General Chemistry
Cited by
44 articles.
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