催化作用
甲醇
氧化剂
材料科学
产量(工程)
金属
氧气
化学工程
无机化学
化学
冶金
有机化学
工程类
作者
Rui Zhang,Xiao Wang,Ke Wang,Huilin Wang,Xudong Sun,Weidong Shi,Shuyan Song,Hongjie Zhang
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2024-12-04
卷期号:10 (49)
标识
DOI:10.1126/sciadv.adr3332
摘要
Converting CO 2 to methanol is crucial for addressing fuel scarcity and mitigating the greenhouse effect. Cu-based catalysts, with their diverse surface states, offer the potential to control reaction pathways and generate reactive H* species. However, a major challenge lies in oxidizing active Cu 0 species by water generated during the catalytic process. While nonreducible metal oxides are beneficial in stabilizing metallic states, their limited capability to generate surface oxygen vacancies (O V ) hinders CO 2 activation. Herein, we present a strategy by doping Nd into a La 2 O 2 CO 3 (LOC) support, enhancing O V formation by disrupting its lattice dyadicity. This leads to higher Cu 0 concentration and improved CO 2 activation. The resulting Cu/LOC:Nd catalyst notably outperforms Cu/LOC and CuZnAl catalysts, achieving a methanol yield of 9.9 moles of methanol per hour per mole of Cu. Our approach opens up possibilities for enhancing Cu-based catalysts in CO 2 conversion.
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