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Related Concept Videos

Thermal and Photochemical Electrocyclic Reactions: Overview01:26

Thermal and Photochemical Electrocyclic Reactions: Overview

Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
Processes at Electrodes01:30

Processes at Electrodes

The electrode interacts with ions in the electrolyte solution at its interface. The rate of oxidation and reduction depends on the speed at which electrons can transfer through this interface. As ions attach to or leave the electrode surface, the electrode acquires a charge, and an electrical potential forms across the interface, making the process more difficult to reach equilibrium. The charge on the electrode affects the local ion concentrations in the solution, though thermal motion...
Types of Reversible Electrodes01:24

Types of Reversible Electrodes

For electrode reversibility to be maintained, all the reactants and products involved in the half-reaction must be present at the electrode. There are several types of reversible electrodes (half-cells).In metal-metal-ion electrodes, a metal balances electrochemically with a solution of its own ions. Examples are Cu2+|Cu and Zn2+|Zn. Metals that react with the solvent, like group 1 and most group 2 metals, which react with water, and zinc, which reacts with aqueous acidic solutions, cannot be...
Electrochemical Systems01:24

Electrochemical Systems

Electrochemical systems provide a fascinating insight into the dynamic interplay of charged species within various phases. One notable example is the interaction between a membrane permeable to K⁺ ions but not to Cl⁻ ions, separating an aqueous KCl solution from pure water. As K⁺ ions diffuse through the membrane, they generate net charges on each phase, leading to a potential difference between them.Similarly, when a piece of Zn is immersed in an aqueous ZnSO₄ solution, the Zn metal, composed...
Controlled-Potential Coulometry: Electrolytic Methods01:17

Controlled-Potential Coulometry: Electrolytic Methods

Controlled-potential coulometry, also known as potentiostatic coulometry, employs a three-electrode system in which the working electrode's potential is precisely regulated using a potentiostat. Platinum working electrodes are utilized for positive potentials, while mercury pool electrodes are favored for extremely negative potentials. The platinum counter electrode is separated from the analyte using a membrane or salt bridge to avoid interference in the analysis.
The chosen potential ensures...
Photochemical Electrocyclic Reactions: Stereochemistry01:26

Photochemical Electrocyclic Reactions: Stereochemistry

The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation

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In Situ Neutron Powder Diffraction Using Custom-made Lithium-ion Batteries
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Operando Electrochemical Phase Engineering Overcomes Activity-Stability Trade-Off in Perovskite Electrocatalysts.

Shiqing Hu1,2, Bingjie Pang1,3, Wei Tu1,4

  • 1State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, Liaoning, China.

Angewandte Chemie (International Ed. in English)
|July 10, 2026
PubMed
Summary
This summary is machine-generated.

This study introduces electrochemical phase engineering (ECPE) to regenerate electrocatalyst active sites during operation. This method overcomes the activity-stability trade-off, enhancing performance in electrochemical devices.

Keywords:
CO2 electroreductionelectrocatalyst regenerationperovskite oxidephase engineeringsolid oxide electrolysis cells

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Catalysis

Background:

  • Electrocatalysts face a critical activity-stability trade-off, limiting device performance.
  • Highly active sites often degrade rapidly under operating conditions.
  • Developing stable and active electrocatalysts is crucial for energy conversion technologies.

Purpose of the Study:

  • To develop a strategy for dynamic regeneration of electrocatalyst active sites.
  • To overcome the inherent activity-stability limitations in electrocatalysts.
  • To demonstrate a novel approach for enhancing the durability of solid oxide electrolysis cells.

Main Methods:

  • Operando electrochemical phase engineering (ECPE) was employed.
  • A perovskite cathode (Sr₂Fe₁.₅Mo₀.₅O₆‒δ) in solid oxide electrolysis cells was investigated.
  • Operando X-ray diffraction and electron microscopy were used to analyze structural evolution.

Main Results:

  • Cathodic polarization induced reversible phase transitions, regenerating active sites within minutes.
  • The dynamic phase switching redistributed exsolved Fe nanoparticles and segregated inactive phases.
  • The engineered cathode sustained efficient CO₂ electroreduction for over 2100 hours with high Faradaic efficiency.

Conclusions:

  • ECPE effectively breaks the activity-stability trade-off in electrocatalysts.
  • This strategy offers a promising framework for durable and efficient electrochemical energy conversion.
  • The dynamic regeneration mechanism provides insights into designing next-generation electrocatalysts.