Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Alkali Metals03:06

Alkali Metals

18.9K
Group 1 elements are soft and shiny metallic solids. They are malleable, ductile, and good conductors of heat and electricity. The melting points of the alkali metals are unusually low for metals and decrease going down the group, while the density increases going down the group with the exception of potassium (Table 1).
Table 1: Properties of the alkali metals
18.9K
Reduction of Alkenes: Catalytic Hydrogenation02:13

Reduction of Alkenes: Catalytic Hydrogenation

11.6K
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...
11.6K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

3.2K
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...
3.2K
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride01:26

Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride

1.8K
Radical substitution reactions can be used to remove functional groups from molecules. The hydrogenolysis of alkyl halides is one such reaction, where the weak Sn–H bond in tributyltin hydride reacts with alkyl halides to form alkanes. Here, the reagent Bu3SnH yields tributyltin halide as a byproduct.
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
1.8K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Dense crystalline-amorphous heterointerface catalysts for freshwater/seawater splitting and small molecule synergistic electrolysis.

Chemical communications (Cambridge, England)·2026
Same author

Poisoning-Resistant Complete Hydrogenation of Liquid Organic Hydrogen Carriers Over Ni-Based Inverse Catalysts.

Angewandte Chemie (International ed. in English)·2026
Same author

Mn-Induced Support Stabilization and Ir Electronic Activation Enable Acid-Stable, Low-Loading IrO<sub>2</sub> Water Oxidation.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026
Same author

Recent Research Progress on Two-Dimensional Organic Framework Materials for Electrocatalytic Carbon Dioxide Reduction Applications.

Small (Weinheim an der Bergstrasse, Germany)·2026
Same author

Assessing the Neuro- and Immunotoxicity of Dissolved Ru<sup>3+</sup> from Proton Exchange Membrane Electrolyzers by Zebrafish Models.

ACS applied materials & interfaces·2026
Same author

Sm-doped RuO<sub>2</sub> electrocatalysts for an acidic oxygen evolution reaction: enhanced activity and stability <i>via</i> electronic structure modulation and oxygen vacancy introduction.

Dalton transactions (Cambridge, England : 2003)·2025

相关实验视频

Updated: May 10, 2025

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
06:32

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions

Published on: August 17, 2016

19.5K

表面单原子合金用于性的进化反应反应.

Li Xu1,2, Yanping Xu3, Bin Xia4

  • 1Department of Chemistry, City University of Hong Kong, Hong Kong SAR, 999077, China.

Advanced materials (Deerfield Beach, Fla.)
|April 22, 2025
PubMed
概括

表面单原子合金 (SSAA) 集成单原子催化剂和单原子合金. 新的Pt1-MoL-Mo2C SSAA显示了增强的性演化反应 (HER) 性能,为先进的单位催化剂设计提供了洞察力.

关键词:
自由-原子-类似的d状态气演化反应反应的反应碳化物可能是碳化物.单个原子催化剂的催化剂.表面的单原子合金.

更多相关视频

Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
08:40

Synthesis 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

3.4K
Simple Methods for the Preparation of Non-noble Metal Bulk-electrodes for Electrocatalytic Applications
09:18

Simple Methods for the Preparation of Non-noble Metal Bulk-electrodes for Electrocatalytic Applications

Published on: June 21, 2017

11.4K

相关实验视频

Last Updated: May 10, 2025

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
06:32

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions

Published on: August 17, 2016

19.5K
Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
08:40

Synthesis 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

3.4K
Simple Methods for the Preparation of Non-noble Metal Bulk-electrodes for Electrocatalytic Applications
09:18

Simple Methods for the Preparation of Non-noble Metal Bulk-electrodes for Electrocatalytic Applications

Published on: June 21, 2017

11.4K

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) 提供100%的金属原子利用率和支持效果.
  • 由于金属键,单原子合金 (SAA) 具有类似自由原子的电子结构.

研究的目的:

  • 开发表面单原子合金 (SSAA),结合SAC和SAA的优势.
  • 研究用于演化反应 (HER) 的 Pt1-MoL-Mo2C SSAA 的结构和催化特性.

主要方法:

  • 通过加入超薄金属层来合成SSAA.
  • 使用综合光谱技术进行表征.
  • 理论计算以阐明电子结构和反应机制.

主要成果:

  • Pt单个原子优先与金属Mo纳米层协调,在Mo2C上形成Pt1-MoL表面合金.
  • 莫纳米层充当了电子缓冲器,在Pt1位点创建了一个类似自由原子的d状态.
  • 观察到H2O的增强聚合,吸附和激活.
  • Pt1-MoL-Mo2C SSAAs表现出优于Pt1/Mo2C SACs的性HER性能,具有12 mV的超电位和17 mV的dec-1的Tafel斜率.

结论:

  • SSAA有效地整合了SAC和SAA的好处.
  • 设计的SSAA在性介质中表现出极好的HER活性.
  • 这项工作为设计先进的单位催化剂提供了新的策略.