Weixin Huang, Hao Xu, Yang Deng, Shih-Wei Lin, Hien N. Pham, Rui Zhang, Dong Jiang, Zihao Zhang, Andrew DeLaRiva, Shuxuan Feng, Yixiao Li, Xinrui Zhang, Abhaya K. Datye, Chih-Jung Chen, Yong Wang
{"title":"单原子Zr助剂促进氧化铈负载Pt催化剂的氧活化","authors":"Weixin Huang, Hao Xu, Yang Deng, Shih-Wei Lin, Hien N. Pham, Rui Zhang, Dong Jiang, Zihao Zhang, Andrew DeLaRiva, Shuxuan Feng, Yixiao Li, Xinrui Zhang, Abhaya K. Datye, Chih-Jung Chen, Yong Wang","doi":"10.1038/s41467-025-62447-w","DOIUrl":null,"url":null,"abstract":"<p>Activation of surface lattice oxygen and chemisorbed oxygen on catalyst surfaces constitutes a pivotal step in heterogeneous oxidative catalysis. Herein, we report a strategy for enhancing oxygen activation by rational design of catalysts with single-atom promoters. Single-site Zr species in CeO<sub>2</sub> (Zr<sub>1</sub>-CeO<sub>2</sub>) are synthesized using the atom-trapping method. The Zr<sub>1</sub>-CeO<sub>2</sub>-supported Pt catalyst exhibits enhanced catalytic performance over the CeO<sub>2</sub>-supported Pt catalyst in the oxidation of CO, C<sub>3</sub>H<sub>8</sub>, and C<sub>3</sub>H<sub>6</sub>, achieving significantly lower T<sub>50</sub> values (temperature required to reach 50% conversion). This enhanced catalytic activity is attributed to the formation of an asymmetric Zr<sub>1</sub>-O-Pt<sub>1</sub> structure, which favors the activation of the adjacent surface lattice oxygen and chemisorbed molecular oxygen. This work exemplifies that incorporating single-site atoms into oxide support facilitates oxygen activation, providing new insights into the role of atomically dispersed promoters in heterogeneous catalysis.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"158 1","pages":""},"PeriodicalIF":15.7000,"publicationDate":"2025-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Single-atom Zr promoter boosts oxygen activation on ceria-supported Pt catalysts\",\"authors\":\"Weixin Huang, Hao Xu, Yang Deng, Shih-Wei Lin, Hien N. Pham, Rui Zhang, Dong Jiang, Zihao Zhang, Andrew DeLaRiva, Shuxuan Feng, Yixiao Li, Xinrui Zhang, Abhaya K. Datye, Chih-Jung Chen, Yong Wang\",\"doi\":\"10.1038/s41467-025-62447-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Activation of surface lattice oxygen and chemisorbed oxygen on catalyst surfaces constitutes a pivotal step in heterogeneous oxidative catalysis. Herein, we report a strategy for enhancing oxygen activation by rational design of catalysts with single-atom promoters. Single-site Zr species in CeO<sub>2</sub> (Zr<sub>1</sub>-CeO<sub>2</sub>) are synthesized using the atom-trapping method. The Zr<sub>1</sub>-CeO<sub>2</sub>-supported Pt catalyst exhibits enhanced catalytic performance over the CeO<sub>2</sub>-supported Pt catalyst in the oxidation of CO, C<sub>3</sub>H<sub>8</sub>, and C<sub>3</sub>H<sub>6</sub>, achieving significantly lower T<sub>50</sub> values (temperature required to reach 50% conversion). This enhanced catalytic activity is attributed to the formation of an asymmetric Zr<sub>1</sub>-O-Pt<sub>1</sub> structure, which favors the activation of the adjacent surface lattice oxygen and chemisorbed molecular oxygen. This work exemplifies that incorporating single-site atoms into oxide support facilitates oxygen activation, providing new insights into the role of atomically dispersed promoters in heterogeneous catalysis.</p>\",\"PeriodicalId\":19066,\"journal\":{\"name\":\"Nature Communications\",\"volume\":\"158 1\",\"pages\":\"\"},\"PeriodicalIF\":15.7000,\"publicationDate\":\"2025-08-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Communications\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1038/s41467-025-62447-w\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-62447-w","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Single-atom Zr promoter boosts oxygen activation on ceria-supported Pt catalysts
Activation of surface lattice oxygen and chemisorbed oxygen on catalyst surfaces constitutes a pivotal step in heterogeneous oxidative catalysis. Herein, we report a strategy for enhancing oxygen activation by rational design of catalysts with single-atom promoters. Single-site Zr species in CeO2 (Zr1-CeO2) are synthesized using the atom-trapping method. The Zr1-CeO2-supported Pt catalyst exhibits enhanced catalytic performance over the CeO2-supported Pt catalyst in the oxidation of CO, C3H8, and C3H6, achieving significantly lower T50 values (temperature required to reach 50% conversion). This enhanced catalytic activity is attributed to the formation of an asymmetric Zr1-O-Pt1 structure, which favors the activation of the adjacent surface lattice oxygen and chemisorbed molecular oxygen. This work exemplifies that incorporating single-site atoms into oxide support facilitates oxygen activation, providing new insights into the role of atomically dispersed promoters in heterogeneous catalysis.
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.