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Incorporation of Epoxy Carbon onto CeO 2 -Supported Pt to Tackle the CO Self-Poisoning Issue.

Jianghao ZhangChuo DuShuchao GeYifan JinShuo HuHongfei XiaoXiaoxiao QinKunlin LiXueyan ChenMin ChenJinhou FangChangbin Zhang
Published in: ACS applied materials & interfaces (2023)
The catalytic oxidation of carbon monoxide (CO) under ambient conditions plays a crucial role in the abatement of indoor CO, which poses risks to human health. Despite the notable activity exhibited by Pt-based catalysts in CO oxidation, their efficacy is usually diminished by the CO self-poisoning issue. In this work, three different Pt/CeO 2 -based catalysts, which have distinct coordinative environments of Pt but an identical Pt/CeO 2 substrate structure, were synthesized by activating the catalyst with CO using different temperatures and durations. Compared with clean and graphite-covered Pt on CeO 2 , the one modified by epoxy carbon showed higher activity and stability. The combination of characterizations and density functional theory modeling demonstrated that the clean Pt on CeO 2 rapidly deactivated due to the CO self-poisoning albeit high initial activity, and conversely, low initial activity was observed for the more stable graphite-covered catalyst due to the obstruction of the Pt site. In contrast, epoxy carbon species on Pt shifted the d-band of Pt to lower energy, weakening the Pt-CO binding strength. Such a modification mitigated the self-poisoning effect while maintaining ample active sites and enabling the complete oxidative removal of CO under ambient conditions. This work may provide a general approach to tackling the self-poisoning issue.
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