Yake Lou, Qianqiu Wu, Jia Shen, Núria J. Divins, Jordi Llorca, Yanglong Guo, Wangcheng Zhan, Aiyong Wang, Li Wang, Yun Guo
{"title":"铋通过调节反应物吸附和反应路线,促进CO对Pt/Al2O3的优先氧化","authors":"Yake Lou, Qianqiu Wu, Jia Shen, Núria J. Divins, Jordi Llorca, Yanglong Guo, Wangcheng Zhan, Aiyong Wang, Li Wang, Yun Guo","doi":"10.1016/j.cej.2025.159751","DOIUrl":null,"url":null,"abstract":"Preferential oxidation of CO (CO-PROX) reaction is an attractive option for hydrogen purification, where the most commonly used Pt-based catalysts suffer from unsatisfactory low-temperature activity. Here, bismuth (Bi) was introduced to improve the catalytic performance of Pt/Al<sub>2</sub>O<sub>3</sub> for the CO-PROX reaction, and the CO conversion of Pt-0.5 wt% Bi/Al<sub>2</sub>O<sub>3</sub> was threefold higher than that of Pt/Al<sub>2</sub>O<sub>3</sub> at around 80 °C and CO could be completely oxidized in the range of 112–175 °C with theoretical O<sub>2</sub> selectivity (50 %). Besides, the Pt-0.5 wt% Bi/Al<sub>2</sub>O<sub>3</sub> exhibited great stability even in the presence of CO<sub>2</sub> and H<sub>2</sub>O. The characterization results showed that Pt tended to selectively deposit on Bi<sub>2</sub>O<sub>3</sub>, which further decreased CO adsorption intensity due to electron transfer from Pt to Bi. Meanwhile, O<sub>2</sub> activation can be strengthened at the Pt-O-Bi interface and the competitive adsorption between CO and H<sub>2</sub> can also be tuned. The presence of Bi strengthened the promotion effect of H<sub>2</sub> and further promoted the generation of HCOO– species, which were the active intermediates of the CO-PROX reaction.","PeriodicalId":270,"journal":{"name":"Chemical Engineering Journal","volume":"12 1","pages":""},"PeriodicalIF":13.2000,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bismuth Boosts the Preferential oxidation of CO over Pt/Al2O3 by Regulating the Reactant adsorption and reaction route\",\"authors\":\"Yake Lou, Qianqiu Wu, Jia Shen, Núria J. Divins, Jordi Llorca, Yanglong Guo, Wangcheng Zhan, Aiyong Wang, Li Wang, Yun Guo\",\"doi\":\"10.1016/j.cej.2025.159751\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Preferential oxidation of CO (CO-PROX) reaction is an attractive option for hydrogen purification, where the most commonly used Pt-based catalysts suffer from unsatisfactory low-temperature activity. Here, bismuth (Bi) was introduced to improve the catalytic performance of Pt/Al<sub>2</sub>O<sub>3</sub> for the CO-PROX reaction, and the CO conversion of Pt-0.5 wt% Bi/Al<sub>2</sub>O<sub>3</sub> was threefold higher than that of Pt/Al<sub>2</sub>O<sub>3</sub> at around 80 °C and CO could be completely oxidized in the range of 112–175 °C with theoretical O<sub>2</sub> selectivity (50 %). Besides, the Pt-0.5 wt% Bi/Al<sub>2</sub>O<sub>3</sub> exhibited great stability even in the presence of CO<sub>2</sub> and H<sub>2</sub>O. The characterization results showed that Pt tended to selectively deposit on Bi<sub>2</sub>O<sub>3</sub>, which further decreased CO adsorption intensity due to electron transfer from Pt to Bi. Meanwhile, O<sub>2</sub> activation can be strengthened at the Pt-O-Bi interface and the competitive adsorption between CO and H<sub>2</sub> can also be tuned. The presence of Bi strengthened the promotion effect of H<sub>2</sub> and further promoted the generation of HCOO– species, which were the active intermediates of the CO-PROX reaction.\",\"PeriodicalId\":270,\"journal\":{\"name\":\"Chemical Engineering Journal\",\"volume\":\"12 1\",\"pages\":\"\"},\"PeriodicalIF\":13.2000,\"publicationDate\":\"2025-01-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Engineering Journal\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1016/j.cej.2025.159751\",\"RegionNum\":1,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, CHEMICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Engineering Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1016/j.cej.2025.159751","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
Bismuth Boosts the Preferential oxidation of CO over Pt/Al2O3 by Regulating the Reactant adsorption and reaction route
Preferential oxidation of CO (CO-PROX) reaction is an attractive option for hydrogen purification, where the most commonly used Pt-based catalysts suffer from unsatisfactory low-temperature activity. Here, bismuth (Bi) was introduced to improve the catalytic performance of Pt/Al2O3 for the CO-PROX reaction, and the CO conversion of Pt-0.5 wt% Bi/Al2O3 was threefold higher than that of Pt/Al2O3 at around 80 °C and CO could be completely oxidized in the range of 112–175 °C with theoretical O2 selectivity (50 %). Besides, the Pt-0.5 wt% Bi/Al2O3 exhibited great stability even in the presence of CO2 and H2O. The characterization results showed that Pt tended to selectively deposit on Bi2O3, which further decreased CO adsorption intensity due to electron transfer from Pt to Bi. Meanwhile, O2 activation can be strengthened at the Pt-O-Bi interface and the competitive adsorption between CO and H2 can also be tuned. The presence of Bi strengthened the promotion effect of H2 and further promoted the generation of HCOO– species, which were the active intermediates of the CO-PROX reaction.
期刊介绍:
The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.