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

Interfacial Electrochemical Methods: Overview01:06

Interfacial Electrochemical Methods: Overview

250
Interfacial electrochemical methods focus on the phenomena occurring at the boundary between an electrode and a solution, as opposed to bulk methods that concentrate on the solution's overall properties. These interfacial methods are classified as either static or dynamic based on the presence of a nonzero current in the electrochemical cell and the consistency of analyte concentrations. Static methods, such as potentiometry, measure the cell's potential without any significant current...
250
Theories of Dissolution: The Danckwerts' Model and Interfacial Barrier Model01:09

Theories of Dissolution: The Danckwerts' Model and Interfacial Barrier Model

309
Various dissolution theories provide insight into the factors that influence the dissolution rate. Danckwerts' Model suggests that turbulence, rather than a stagnant layer, characterizes the dissolution medium at the solid-liquid interface. In this model, the agitated solvent contains macroscopic packets that move to the interface via eddy currents, facilitating the absorption and delivery of the drug to the bulk solution. The regular replenishment of solvent packets maintains the...
309
Formation of Complex Ions03:45

Formation of Complex Ions

23.7K
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...
23.7K
Electrochemistry: Overview01:04

Electrochemistry: Overview

2.0K
Electrochemistry is the branch of chemistry that studies the relationship between electrical quantities and chemical reactions, particularly oxidation and reduction. Oxidation is the loss of electrons from a substance, whereas reduction refers to the gain of electrons. A substance with a strong electron affinity is called an oxidizing agent (oxidant), and a reducing agent (reductant) is a species that donates electrons. Oxidation and reduction processes are pivotal to electrochemical reactions,...
2.0K
Energetics of Solution Formation02:35

Energetics of Solution Formation

6.7K
The formation of a solution is an example of a spontaneous process, which is a process that occurs under specified conditions without energy from some external source.
When the strengths of the intermolecular forces of attraction between solute and solvent species in a solution are no different than those present in the separated components, the solution is formed with no accompanying energy change. Formation of the solution requires the solute–solute and solvent–solvent...
6.7K
Intermolecular Forces03:13

Intermolecular Forces

58.4K
Atoms and molecules interact through bonds (or forces): intramolecular and intermolecular. The forces are electrostatic as they arise from interactions (attractive or repulsive) between charged species (permanent, partial, or temporary charges) and exist with varying strengths between ions, polar, nonpolar, and neutral molecules. The different types of intermolecular forces are ion–dipole, dipole–dipole, hydrogen bonds, and dispersion; among these, dipole–dipole, hydrogen...
58.4K

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

Dynamic Proton Transfer Competition and pH-Dependent ORR Mechanism in γN-Modulated Fe-N-C Single-Atom Catalysts.

Inorganic chemistry·2026
Same author

A saddle-shaped OBO-doped nanographene: facile synthesis, adaptive double-layer assembly, and enhanced Lewis acidity.

Chemical science·2026
Same author

Observation of Structurally Diverse Complexes OCeNi(CO)<sub>3</sub><sup>-</sup> and CeNi(CO)<sub>3</sub><sup>-</sup> with the Shortest Ce-Ni Bond and Ce≡O Triple Bond.

The journal of physical chemistry letters·2026
Same author

Highly Selective Purification of Trace <sup>131</sup>I in Radioactive Wastewater via Adaptive Inflatable Organic Cages with Fully Accessible Sites.

Inorganic chemistry·2026
Same author

Development and comparative study of a hydrophilic bis-triazolyl-phenanthroline ligand and two bis-triazolyl-pyridine ligands.

Dalton transactions (Cambridge, England : 2003)·2026
Same author

Fine-Tuning the Coordination Structure and Identifying Pt<sub>1</sub>-O<sub>v</sub>-Ce as the Active Site for Selective Hydrogenations over Pt<sub>1</sub>/CeO<sub>2</sub> Single-Atom Catalysts.

Journal of the American Chemical Society·2026

相关实验视频

Updated: Jul 6, 2025

Multiscale Sampling of a Heterogeneous Water/Metal Catalyst Interface using Density Functional Theory and Force-Field Molecular Dynamics
10:52

Multiscale Sampling of a Heterogeneous Water/Metal Catalyst Interface using Density Functional Theory and Force-Field Molecular Dynamics

Published on: April 12, 2019

12.8K

在单原子电催化剂上建模界面动力学:明确的溶解和潜在依赖.

Zisheng Zhang1, Jun Li2, Yang-Gang Wang

  • 1Department of Chemistry and Biochemistry, University of California, Los Angeles, Los Angeles, California 90095, United States.

Accounts of chemical research
|January 3, 2024
PubMed
概括
此摘要是机器生成的。

单原子电催化剂是复杂的,接口动态显著影响其性能. 现实的建模对于理解和优化这些高贵的无金属催化剂的能源和环境应用至关重要.

更多相关视频

Precise Electrochemical Sizing of Individual Electro-Inactive Particles
05:03

Precise Electrochemical Sizing of Individual Electro-Inactive Particles

Published on: August 4, 2023

1.2K
Unraveling Entropic Rate Acceleration Induced by Solvent Dynamics in Membrane Enzymes
09:42

Unraveling Entropic Rate Acceleration Induced by Solvent Dynamics in Membrane Enzymes

Published on: January 16, 2016

9.0K

相关实验视频

Last Updated: Jul 6, 2025

Multiscale Sampling of a Heterogeneous Water/Metal Catalyst Interface using Density Functional Theory and Force-Field Molecular Dynamics
10:52

Multiscale Sampling of a Heterogeneous Water/Metal Catalyst Interface using Density Functional Theory and Force-Field Molecular Dynamics

Published on: April 12, 2019

12.8K
Precise Electrochemical Sizing of Individual Electro-Inactive Particles
05:03

Precise Electrochemical Sizing of Individual Electro-Inactive Particles

Published on: August 4, 2023

1.2K
Unraveling Entropic Rate Acceleration Induced by Solvent Dynamics in Membrane Enzymes
09:42

Unraveling Entropic Rate Acceleration Induced by Solvent Dynamics in Membrane Enzymes

Published on: January 16, 2016

9.0K

科学领域:

  • 电触媒溶解是一种电触媒.
  • 材料科学 材料科学 材料科学
  • 物理化学 物理化学

背景情况:

  • 单原子电催化剂 (SAEC) 由于其高原子效率和反应性,对能源和环境应用至关重要.
  • 它们的简单结构使得它们非常适合研究反应机制,但它们在电化学条件下的行为是复杂的.
  • 接口动力学,包括溶剂和电解质离子相互作用,显著影响SAEC活性位点.

研究的目的:

  • 研究电化学反应期间影响单原子电催化剂的复杂界面动力学.
  • 为了证明电化学潜能如何影响反应通路和中间稳定.
  • 通过结合接口因素来修改SAEC的简单设计原则.

主要方法:

  • 分析受欢迎的单原子电催化系统.
  • 电化学潜力对自由能量概况的影响的建模.
  • 研究溶解结构和界面现象.

主要成果:

  • 电化学潜能会导致反应自由能量概况的显著变化.
  • 活跃中心电子结构决定了界面溶解,影响了反应中间体.
  • 溶解和极化效应可以有利于替代反应路径和动态位点激活/停用.

结论:

  • 现实的建模,包括明确的溶剂,电解质和电极潜力,对于准确理解SAEC机制和趋势是必要的.
  • 接口的复杂性为SAEC的更精细控制和优化提供了机会.
  • 目前简单的设计原则需要修订,以考虑动力学和界面因素.