Novel and active Bi2Zr1.9M0.1O7 (M = Mn, Fe, Co, Ni) catalysts for soot particle removal: Engineering surface with rich oxygen defects via partial substitution of Zr-site
{"title":"Novel and active Bi2Zr1.9M0.1O7 (M = Mn, Fe, Co, Ni) catalysts for soot particle removal: Engineering surface with rich oxygen defects via partial substitution of Zr-site","authors":"Shijing Zhang, Ping Wang, Yuting Li, Haojun Liu, Jiating Shen, Xianglan Xu, Junwei Xu, Xiuzhong Fang, Xiang Wang","doi":"10.1002/ece2.64","DOIUrl":null,"url":null,"abstract":"<p>To obtain more cost-effective, non-noble catalysts for soot particle combustion of diesel engine cars, Bi<sub>2</sub>Zr<sub>1.9</sub>M<sub>0.1</sub>O<sub>7</sub> (M = Mn, Fe, Co, Ni) compounds with partial lattice substitution have been designed and synthesized. All the substituted catalysts show significantly promoted activity, in the order of Bi<sub>2</sub>Zr<sub>2</sub>O<sub>7</sub> < Bi<sub>2</sub>Zr<sub>1.9</sub>Ni<sub>0.1</sub>O<sub>7</sub> < Bi<sub>2</sub>Zr<sub>1.9</sub>Co<sub>0.1</sub>O<sub>7</sub> < Bi<sub>2</sub>Zr<sub>1.9</sub>Fe<sub>0.1</sub>O<sub>7</sub> < Bi<sub>2</sub>Zr<sub>1.9</sub>Mn<sub>0.1</sub>O<sub>7</sub>. The presence of NO improves the activity of all the samples due to the generation of active surface nitrates/nitrites. It has been proven that all the modified catalysts possess weaker Zr–O bonds, which facilitates the generation of more surface defects. Density functional theory calculations have confirmed that a more defective catalyst has a lower vacancy formation energy and O<sub>2</sub> adsorption energy. Isotopic <sup>18</sup>O<sub>2</sub> labeling has also substantiated that a more defective catalyst has a faster gaseous O<sub>2</sub> exchange rate, thus improving the generation of more abundant soot reactive oxygen sites. The weakening of Zr-O bonds is the inherent factor to improve the catalytic activity. Mn-substitution can lead to the weakest Zr-O bonds in Bi<sub>2</sub>Zr<sub>1.9</sub>Mn<sub>0.1</sub>O<sub>7</sub>, which thus shows the optimal catalytic activity. Notably, the complete soot combustion can be achieved even at 360°C on this catalyst.</p>","PeriodicalId":100387,"journal":{"name":"EcoEnergy","volume":"2 4","pages":"736-748"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ece2.64","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"EcoEnergy","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ece2.64","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
To obtain more cost-effective, non-noble catalysts for soot particle combustion of diesel engine cars, Bi2Zr1.9M0.1O7 (M = Mn, Fe, Co, Ni) compounds with partial lattice substitution have been designed and synthesized. All the substituted catalysts show significantly promoted activity, in the order of Bi2Zr2O7 < Bi2Zr1.9Ni0.1O7 < Bi2Zr1.9Co0.1O7 < Bi2Zr1.9Fe0.1O7 < Bi2Zr1.9Mn0.1O7. The presence of NO improves the activity of all the samples due to the generation of active surface nitrates/nitrites. It has been proven that all the modified catalysts possess weaker Zr–O bonds, which facilitates the generation of more surface defects. Density functional theory calculations have confirmed that a more defective catalyst has a lower vacancy formation energy and O2 adsorption energy. Isotopic 18O2 labeling has also substantiated that a more defective catalyst has a faster gaseous O2 exchange rate, thus improving the generation of more abundant soot reactive oxygen sites. The weakening of Zr-O bonds is the inherent factor to improve the catalytic activity. Mn-substitution can lead to the weakest Zr-O bonds in Bi2Zr1.9Mn0.1O7, which thus shows the optimal catalytic activity. Notably, the complete soot combustion can be achieved even at 360°C on this catalyst.