Abstract |
Rational design of low-cost and efficient transition-metal catalysts for low-temperature CO2 activation is significant and poses great challenges. Herein, a strategy via regulating the local electron density of active sites is developed to boost CO2 methanation that normally requires >350 °C for commercial Ni catalysts. An optimal Ni/ZrO2 catalyst affords an excellent low-temperature performance hitherto, with a CO2 conversion of 84.0 %, CH4 selectivity of 98.6 % even at 230 °C and GHSV of 12,000 mL g-1 h-1 for 106 h, reflecting one of the best CO2 methanation performance to date on Ni-based catalysts. Combined a series of in situ spectroscopic characterization studies reveal that re-constructing monoclinic-ZrO2 supported Ni species with abundant oxygen vacancies can facilitate CO2 activation, owing to the enhanced local electron density of Ni induced by the strong metal-support interactions. These findings might be of great aid for construction of robust catalysts with an enhanced performance for CO2 emission abatement and beyond. |
Authors |
Run‐Ping Ye , Li Ma , Xiaoling Hong , Tomás Ramı́rez Reina , Wenhao Luo , Liqun Kang , Gang Feng , Rongbin Zhang , Maohong Fan  , Riguang Zhang , Jian Liu
|
Journal Info |
Wiley | Angewandte Chemie , vol: 63
, iss: 3
|
Publication Date |
12/8/2023 |
ISSN |
1433-7851 |
Type |
article |
Open Access |
hybrid
|
DOI |
https://doi.org/10.1002/anie.202317669 |
Keywords |
CO2 Conversion (Score: 0.589515) , Methane Activation (Score: 0.569598) , Homogeneous Catalysts (Score: 0.524579) , NOx Reduction (Score: 0.521898) , Hydrogenation (Score: 0.504812)
|