Sacrificial Adsorbate Strategy Achieved Strong Metal–Support Interaction of Stable Cu Nanocatalysts
Source abstract
Abstract
A new adsorbate-mediated strategy was developed to enhance the metal–support interaction of Cu/CeO2, aiming to improve its catalytic activity and sintering resistance in the water–gas shift (WGS) reaction. By treating Cu/CeO2 in a 20CO2/2H2 gas mixture for the formation of surface HCOn (n = 2, 3), there was significant enhancement of the interaction between CeO2 and Cu. The HCOn adsorbate was removed through calcination in an O2/Ar atmosphere at 400 °C for 6 h. The as-obtained Cu/CeO2 catalyst was compared with the untreated counterpart in the WGS reaction. It was observed that CO conversion at 350 °C was 86% and 47%, respectively, over the two catalysts. The superiority of the former is attributed to the enhanced interaction between Cu and CeO2. In a run of 15 h at 400 °C, the treated catalyst showed no obvious sign of deactivation.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Catalytic Processes in Materials Science · Catalysts for Methane Reforming · Nanomaterials for catalytic reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
National Engineering Research Center of Chemical Fertilizer Catalyst, Fuzhou University, Fuzhou, Fujian 350002, China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Fujian Province
References (27)
Show source-provided references
1. 10.1021/acscatal.5b0190910.1021/acscatal.5b01909 ↗
2. 10.1021/ja110705a10.1021/ja110705a ↗
3. 10.1021/acscatal.7b0008610.1021/acscatal.7b00086 ↗
4. 10.1021/ja210083d10.1021/ja210083d ↗
5. 10.1021/ja312646d10.1021/ja312646d ↗
6. 10.1016/j.jcat.2014.03.01510.1016/j.jcat.2014.03.015 ↗
7. 10.1016/j.apcata.2016.01.02710.1016/j.apcata.2016.01.027 ↗
8. 10.1016/j.fuproc.2010.02.00410.1016/j.fuproc.2010.02.004 ↗
9. 10.1039/C6CS00863A10.1039/C6CS00863A ↗
10. 10.1016/j.apcatb.2012.12.01310.1016/j.apcatb.2012.12.013 ↗
11. 10.1038/nmat475710.1038/nmat4757 ↗
12. 10.1021/ja507956m10.1021/ja507956m ↗
13. 10.1021/ja00469a02910.1021/ja00469a029 ↗
14. 10.1016/S0926-860X(97)00221-410.1016/S0926-860X(97)00221-4 ↗
15. 10.1016/j.apcatb.2008.03.01710.1016/j.apcatb.2008.03.017 ↗
16. 10.1016/j.jcat.2010.08.01710.1016/j.jcat.2010.08.017 ↗
17. 10.1039/c2jm31184d10.1039/c2jm31184d ↗
18. 10.1021/acscatal.6b0069810.1021/acscatal.6b00698 ↗
19. 10.1016/j.jcat.2004.11.02710.1016/j.jcat.2004.11.027 ↗
20. 10.1039/C5CY01932J10.1039/C5CY01932J ↗
21. 10.1039/C5CY01885D10.1039/C5CY01885D ↗
22. 10.1021/ja310341j10.1021/ja310341j ↗
23. 10.1016/j.apcata.2017.04.01310.1016/j.apcata.2017.04.013 ↗
24. 10.1016/j.cej.2017.03.03810.1016/j.cej.2017.03.038 ↗
25. 10.1021/ja073926g10.1021/ja073926g ↗
26. 10.1016/j.jcat.2013.10.01910.1016/j.jcat.2013.10.019 ↗
27. 10.1039/b923780a10.1039/b923780a ↗