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Combined in situ X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) studies have been conducted to follow gold structural changes of low-content (<1%Au) gold-ceria catalysts in water-gas shift (WGS) reaction tests at 100 and 200 °C; and after heating the used catalysts in oxygen gas at 150 °C. Gold in the fresh (400 °C-calcined) material was atomically dispersed in cerium oxide. Under WGS reaction conditions, reduction of the oxidized gold species was observed, accompanied by gradual gold aggregation. The Au−Au coordination number is zero for the fresh material, but increases with the reaction temperature, to 6.5 ± 2.4 (after use at 100 °C) and to 8.7 ± 1.5 (after 200 °C) in a gas mixture containing 5% CO- 3% H2O in helium. The second important parameter is the reaction gas composition which determines the extent of Au−O reduction. The lower the reduction potential of the reaction gas mixture, the more oxidized the gold is in the used catalyst, and the higher its activity. The maximum activity of Au-CeO2 was that of the fully dispersed Au−O−Ce fresh material. Loss of surface oxygen took place during reaction, as measured by H2-TPR of the used samples, and it was commensurate with the activity loss. Attempts to reoxidize and redisperse the gold by heating in oxygen gas at 150 °C were not effective. However, we report here that complete recovery of the surface oxygen amount and redispersion of gold in ceria was possible after a 400 °C- oxygen treatment of both the 100 °C- and 200 °C- used catalyst samples, with concomitant recovery of the initial catalyst activity. These tests were conducted by consecutive H2-TPR/steady-state catalyst activity measurements in the same microreactor.
Deng et al. (Wed,) studied this question.