尼克尔单原子催化剂的远程协调工程,以促进CO2的电还原
Mingxia Peng1, Jing Li1, Sili Zhu1
1School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, P. R. China. lijingkun@ecust.edu.cn.
概括
改进单原子催化剂 (Ni-SACs) 的实际使用需要提高它们的内在活性. 使用Cl/S兴奋剂的远程协调工程增强了Ni-SACs.
科学领域:
- 催化剂是一种催化剂.
- 材料科学 材料科学 材料科学
- 电化学 电化学 电化学
背景情况:
- 单原子催化剂 (Ni-SACs) 在二氧化碳电还原 (CO2RR) 方面表现有前途.
- 它们的实际应用受到自身活动不足的限制.
- 优化Ni-SAC的电子结构对于提高性能至关重要.
研究的目的:
- 调查Ni-SACs的远程协调工程.
- 为了增强Ni-SACs在二氧化碳电还原方面的内在活性.
- 为了提高CO2RR对CO的选择性.
主要方法:
- 使用 (Cl) 和硫 (S) 兴奋剂在Ni-SAC的更高阶协调 (≥2) 中.
- 描述Ni-SACs的电子结构调制.
- 评估二氧化碳电还原的电催化性能.
主要成果:
- 通过Cl/S兴奋剂的远程协调工程有效调节Ni-SACs的电子结构.
- 调制电子结构加强了关键中间体 (*COOH) 的结合.
- 实现了增强的CO2RR活动和对CO的选择性.
结论:
- 远程协调工程是一种可行的策略,可以提高Ni-SAC的性能.
- Cl / S 兴奋剂提供了一条优化 Ni-SACs 的途径,以有效地将 CO2 电还原为 CO.
- 这种方法解决了现有的Ni-SAC在实际应用中的局限性.
更多相关视频
08:40Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
Published on: December 6, 2021
4.1K
08:13Chemical Precipitation Method for the Synthesis of Nb2O5 Modified Bulk Nickel Catalysts with High Specific Surface Area
Published on: February 19, 2018
12.4K
相关概念视频
Catalysis
30.1K
The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
30.1K
Metal-Ligand Bonds
23.9K
The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
23.9K
Electrodeposition
1.3K
Electrodeposition is a technique used to separate an analyte from interferents by electrochemical processes. Here, the analyte is a metal ion that can be deposited on an electrode immersed in the sample solution. The electrochemical setup consists of an anode and a cathode. When an electric current is applied to the setup, oxidation occurs at the anode. At the cathode, which consists of a large metal surface, metal ions undergo reduction and deposit onto the surface.
Electrodeposition can...
Electrodeposition can...
1.3K
Coordination Number and Geometry
18.9K
For transition metal complexes, the coordination number determines the geometry around the central metal ion. Table 1 compares coordination numbers to molecular geometry. The most common structures of the complexes in coordination compounds are octahedral, tetrahedral, and square planar.
18.9K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
3.8K
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...
3.8K
Valence Bond Theory
11.2K
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
11.2K
