| Title: | Single-atom Pt-CeO(2)/Co(3)O(4) catalyst with ultra-low Pt loading and high performance for toluene removal |
| Author(s): | Shi H; Yang P; Huang L; Wu Y; Yu D; Wu H; Zhang Y; Xiao P; |
| Address: | "College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, China. Chongqing Key Laboratory of Soft Condensed Matter Physics and Smart Materials, College of Physics, Chongqing University, Chongqing 401331, China. College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, China. Electronic address: zyh2031@cqu.edu.cn. Chongqing Key Laboratory of Soft Condensed Matter Physics and Smart Materials, College of Physics, Chongqing University, Chongqing 401331, China. Electronic address: xiaopeng@cqu.edu.cn" |
| DOI: | 10.1016/j.jcis.2023.03.086 |
| ISSN/ISBN: | 1095-7103 (Electronic) 0021-9797 (Linking) |
| Abstract: | "The design and manufacture of high activity and thermal stability catalysts with minimal precious metal loading is essential for deep degradation of volatile organic compounds (VOCs). In this paper, a novel single-atom Pt-CeO(2)/Co(3)O(4) catalyst with ultra-low Pt loading capacity (0.06 wt%, denoted as 0.06Pt-SA) was fabricated via one-step co-precipitation method. The 0.06Pt-SA exhibited excellent toluene degradation activity of T(90) = 169 degrees C, matched with the nanoparticle Pt-supported CeO(2)/Co(3)O(4) catalyst with more than six times higher Pt loading (0.41 wt%, denoted as 0.41Pt-NP). Moreover, the ultra-long durability (toluene conversion remains 99% after 120 h stability test) and excellent toluene degradation ability in a wide space speed range of 0.06Pt-SA were superior to that of 0.41Pt-NP catalyst. The excellent performance was derived from the strong metal-support interaction (SMSI) between the single atomic Pt and the carrier, which induced more Pt(0) and Ce(3+) for oxygen activation and more Co(3+) for toluene removal. The in situdiffuse reflectance infrared spectroscopy (DRIFTS) experiments confirmed that the conversion of intermediates was accelerated in the reaction process, thereby promoting the toluene degradation. Our results should inspire the exploitation of noble single-atomic modification strategy for developing the low cost and high performance VOCs catalyst" |
| Keywords: | Durability Supported single-atom Pt catalyst Toluene catalytic oxidation Ultra-low Pt loading; |
| Notes: | "PubMed-not-MEDLINEShi, Huihui Yang, Peixin Huang, Lu Wu, Yali Yu, Duohuan Wu, Hangfei Zhang, Yunhuai Xiao, Peng eng 2023/03/30 J Colloid Interface Sci. 2023 Jul; 641:972-980. doi: 10.1016/j.jcis.2023.03.086. Epub 2023 Mar 22" |
