非金属元素调制Co3O4/NiFe-LDH异质连接电催化剂,以实现高效的氧化演化反应
Dipeng Sun1, Yongqi Xu1, Lijie Zang1
1School of Materials Science and Engineering, Shenyang Ligong University, Shenyang 110159, China. lyux@sylu.edu.cn.
概括
在B-Co3O4@NiFe-LDH中化会产生氧气空缺,提高电催化剂的性能. 这种增强材料在性条件下表现出优异的氧化演化反应 (OER) 活性.
科学领域:
- 材料科学 材料科学 材料科学
- 电化学 电化学 电化学
- 催化剂是一种催化剂.
背景情况:
- 异构结构接口对于催化活性至关重要.
- 氧进化反应 (OER) 是能量转化中的一个关键过程.
- 非金属兴奋剂可以修改材料特性,以增强催化作用.
研究的目的:
- 为了研究兴奋剂对Co3O4@NiFe-LDH异构结构的影响.
- 为了评估OER的B-Co3O4@NiFe-LDH的电催化性能.
- 了解氧气空缺和电子再分配在催化中的作用.
主要方法:
- B-Co3O4@NiFe-LDH电催化剂的合成.
- 在性介质中的电化学表征.
- 对材料结构和电子性质的兴奋剂效应的分析.
主要成果:
- 兴奋剂产生氧气空缺并改变异构界面上的电子分布.
- B-Co3O4@NiFe-LDH催化剂在10 mA cm-2.2时表现出115 mV的低OER超电位.
- 与未使用兴奋剂的同行相比,证明了优越的OER活动.
结论:
- 兴奋剂是一种有效的策略,可以增强Co3O4@NiFe-LDH的OER活性.
- 氧气空缺和变化的电子再分配是提高催化性能的关键因素.
- B-Co3O4@NiFe-LDH催化剂对高效的氧气进化应用有很大的希望.
更多相关视频
10:57Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
18.4K
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
3.7K
相关概念视频
Formation of Complex Ions
18.8K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
18.8K
Properties of Transition Metals
28.2K
Transition metals are defined as those elements that have partially filled d orbitals. As shown in Figure 1, the d-block elements in groups 3–12 are transition elements. The f-block elements, also called inner transition metals (the lanthanides and actinides), also meet this criterion because the d orbital is partially occupied before the f orbitals.
28.2K
Metal-Ligand Bonds
19.3K
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...
19.3K
Extraction: Advanced Methods
1.3K
Metal ions can be separated from one another by complexation with organic ligands–the chelating agent– to form uncharged chelates. Here, the chelating agent must contain hydrophobic groups and behave as a weak acid, losing a proton to bind with the metal. Since most organic ligands used in this process are insoluble or undergo oxidation in the aqueous phase, the chelating agent is initially added to the organic phase and extracted into the aqueous phase. The metal-ligand complex is...
1.3K
Heterogeneous Catalysis
141
Heterogeneous catalysis involves a catalyst in a different phase from the reactants. It is a process where the catalyst and the reactants are in distinct phases, typically solid and gas or liquid.Most heterogeneous catalysts are metals, metal oxides, or acids. The list includes transition metals like iron (Fe), cobalt (Co), nickel (Ni), palladium (Pd), platinum (Pt), chromium (Cr), manganese (Mn), tungsten (W), silver (Ag), and copper (Cu). These metals possess partially vacant d orbitals that...
141
Microbes and Other Elemental Cycles
89
Microbial activity plays a pivotal role in the biogeochemical cycling of iron and manganese, especially at the redox gradients characteristic of stratified aquatic environments. These cycles are driven by microbial transformations between oxidized and reduced forms of the metals, allowing organisms to exploit them for metabolic energy and structural purposes.Iron Cycling Across Redox GradientsIn neutral, oxygen-rich surface waters, iron is predominantly found in its oxidized, insoluble ferric...
89
