Ag-N-C单原子催化剂具有抗在乙烯化中对Ag损失的抵抗力
Li Liu1, Fangjie Lu1,2, Xue Yin2
1School of Chemistry and Chemical Engineering of Shihezi University, Shihezi, Xinjiang 832000, People's Republic of China.
Nanotechnology
|October 12, 2023
概括
开发了一种新的银--碳单原子催化剂 (Ag-N-C SAC) 用于乙烯化. 这种Ag-N-C SAC表现出了特殊的稳定性,与传统催化剂相比,显著减少了银损失.
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.
- 纳米技术纳米技术
背景情况:
- 开发稳定高效的催化剂对于工业化工过程至关重要.
- 基于银的催化剂被广泛使用,但往往由于稳定性不佳和泄漏而受到影响.
- 乙烯化是一种重要的工业反应,需要强大的催化系统.
研究的目的:
- 合成和描述一种高度稳定的银--碳单原子催化剂 (Ag-N-C SAC).
- 为了研究催化剂结构内的银稳定机制.
- 为了评估Ag-N-C SAC在乙烯基化中的性能和稳定性.
主要方法:
- 通过化利用酸银,活性碳和胺合成Ag-N-C催化剂.
- 使用偏差校正高角度环状暗场扫描传输电子显微镜 (AC-HAADF-STEM) 进行表征.
- 通过10小时的乙烯化过程评估催化剂稳定性.
主要成果:
- 成功合成了Ag-N-C SAC,其中的银原子与碳支柱中的相协调.
- AC-HAADF-STEM证实了银在单原子形式的存在.
- Ag-N-C SAC表现出了显著的稳定性,白银在10小时内损失率仅为0.09%,明显低于Ag-N-C催化剂 (57%).
结论:
- 银- (Ag-N) 键的形成是稳定银物种的关键.
- Ag-N-C SAC提供了卓越的稳定性,并减少了在乙烯化中银的出.
- 这项研究提出了一个有希望的策略,用于设计工业应用的高度稳定的单原子催化剂.
相关概念视频
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
7.8K
Introduction
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
7.8K
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
Reduction of Alkenes: Catalytic Hydrogenation
12.1K
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...
12.1K
Structure and Physical Properties of Alkynes
10.7K
Introduction:
In nature, compounds containing both carbon and hydrogen are known as "hydrocarbons". Aliphatic hydrocarbons are compounds whose molecules contain saturated single bonds (i.e., alkanes) or unsaturated double or triple bonds. Alkenes contain carbon–carbon double bonds and have a structural formula CnH2n. Unsaturated hydrocarbons containing carbon–carbon triple bonds are called "alkynes" and are structurally represented by the formula CnH2n-2.
The...
In nature, compounds containing both carbon and hydrogen are known as "hydrocarbons". Aliphatic hydrocarbons are compounds whose molecules contain saturated single bonds (i.e., alkanes) or unsaturated double or triple bonds. Alkenes contain carbon–carbon double bonds and have a structural formula CnH2n. Unsaturated hydrocarbons containing carbon–carbon triple bonds are called "alkynes" and are structurally represented by the formula CnH2n-2.
The...
10.7K
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
18.2K
Introduction
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
18.2K
Electrophilic Aromatic Substitution: Friedel–Crafts Acylation of Benzene
7.1K
The Friedel–Crafts acylation reactions involve the addition of an acyl group to an aromatic ring. These reactions proceed via electrophilic aromatic substitution by employing an acyl chloride and a Lewis acid catalyst such as aluminum chloride to form aryl ketone.
7.1K


