单原子的方向增长和密度调节,以实现高效的电催化演变
Xinyang Liu1, Yuxuan Zhou2, Jingkai Lin3
1School of Materials and Chemistry, University of Shanghai for Science and Technology, 200093, Shanghai, P. R. China.
Angewandte Chemie (International ed. in English)
|May 31, 2024
概括
这项研究引入了一种新的方法,将单原子 (PtSA) 在可调节的氧空缺的二氧化 (CeO2-X) 上,增强进化反应 (HER) 催化. 在CeO2-X/rGO上的最佳PtSA分散显著提高了绿色能源应用的催化活性和稳定性.
科学领域:
- 材料科学 材料科学 材料科学
- 催化剂是一种催化剂.
- 电化学 电化学 电化学
背景情况:
- 单原子催化剂 (SAC) 对于优化催化活性至关重要.
- 调整主机材料特性是提高SAC性能的关键.
- 二氧化 (CeO2-X) 是一个有前途的宿主材料,因为它具有氧空位的可调性.
研究的目的:
- 开发一种新的策略,以控制氧气空缺,在CeO2-X上固定单原子 (PtSA).
- 研究CeO2-X密度对演化反应 (HER) 中PtSA的催化性能的影响.
- 为了优化PtSA在CeO2-X/rGO上的分散和加载,以提高HER活动和稳定性.
主要方法:
- PtSA的定向定通过调整CeO2-X中的氧气空缺.
- 在减少的氧化石墨烯 (rGO) 上PtSA的均分散支持CeO2-X.
- 在酸性和性介质中对HER进行电催化测试.
- 进行全面的实验和理论计算以阐明结构-活动关系.
主要成果:
- PtSA均分散在CeO2-X/rGO上,具有可调节的氧气空缺.
- 最佳催化剂 (PtSA-M-CeO2-X/rGO) 显示出优越的 HER 活性,具有较低的超电位 (25 mV 在 0.5 M H2SO4, 33 mV 在 1 M KOH).
- 在酸性和性条件下,在高电流密度下,经过90小时的特殊稳定性.
结论:
- 拟议的战略有效地调整了CeO2-X中的氧气空缺,以定PtSA,从而提高了HER的性能.
- 在缺陷丰富的CeO2-X上优化了PtSA分散,为催化提供了丰富的活性位点.
- 这项工作为通过缺陷工程进行绿色能源转换开发高度活跃和稳定的SAC提供了有希望的途径.
相关概念视频
Reduction of Alkenes: Catalytic Hydrogenation
12.0K
Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a transition-metal catalyst, the reaction is called catalytic hydrogenation.
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
12.0K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
3.3K
Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
3.3K


