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Related Concept Videos

Catalysis02:50

Catalysis

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The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
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Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation02:24

Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation

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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.
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Introduction to Mechanisms of Enzyme Catalysis01:13

Introduction to Mechanisms of Enzyme Catalysis

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For many years, scientists thought that enzyme-substrate binding took place in a simple "lock-and-key" fashion. This model stated that the enzyme and substrate fit together perfectly in one instantaneous step. However, current research supports a more refined view scientists call induced fit. The induced-fit model expands upon the lock-and-key model by describing a more dynamic interaction between enzyme and substrate. As the enzyme and substrate come together, their interaction causes...
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Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

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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...
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Reduction of Alkenes: Catalytic Hydrogenation02:13

Reduction of Alkenes: Catalytic Hydrogenation

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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...
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Thermal and Photochemical Electrocyclic Reactions: Overview01:26

Thermal and Photochemical Electrocyclic Reactions: Overview

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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.
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Related Experiment Video

Updated: Sep 2, 2025

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
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Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction

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Thermally-stable single-atom catalysts and beyond: A perspective.

Sixu Liu1,2, Jiwei Li1,2, Haifeng Xiong1,2

  • 1State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, China.

Frontiers in Chemistry
|August 1, 2022
PubMed
Summary

Developing stable single-atom catalysts (SACs) for high temperatures is challenging. This perspective reviews methods for creating thermally stable SACs via reverse-Ostwald ripening, focusing on atom trapping and self-assembly for improved catalytic performance.

Keywords:
atom trappingmetal-support interactionsingle-atom catalyststhermally stablevapor-phase self-assembly

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Area of Science:

  • Heterogeneous Catalysis
  • Materials Science
  • Surface Chemistry

Background:

  • Single-atom catalysts (SACs) offer high efficiency but struggle with stability at elevated temperatures due to atom sintering.
  • Understanding and overcoming the thermal instability of SACs is crucial for their practical application in high-temperature reactions.
  • Current research focuses on developing robust SACs that maintain their structure and activity under harsh conditions.

Purpose of the Study:

  • To review recent advancements in synthesizing thermally stable SACs for high-temperature applications.
  • To explore synthesis strategies, including atom trapping and vapor-phase self-assembly, based on the reverse-Ostwald ripening mechanism.
  • To provide insights into designing stable and active SACs by correlating structure with performance.

Main Methods:

  • Summarizing recent literature on the preparation of thermally stable SACs synthesized at elevated temperatures.
  • Discussing synthesis approaches such as atom trapping and vapor-phase self-assembly.
  • Integrating experimental findings with computational simulations to analyze catalyst properties.

Main Results:

  • Thermally stable SACs can be prepared via the reverse-Ostwald ripening mechanism, utilizing atom trapping and vapor-phase self-assembly.
  • Key factors like lattice oxygen reducibility, metal loading limits, and single-atom location influence catalyst stability and reactivity.
  • Tailoring the coordination structure of metal single atoms is shown to be effective in optimizing SAC performance.

Conclusions:

  • The reverse-Ostwald ripening mechanism offers a viable route to synthesize thermally stable SACs.
  • Understanding the interplay between synthesis parameters, structure, and high-temperature catalytic performance is essential for rational catalyst design.
  • This perspective provides guidance for developing advanced SACs suitable for demanding high-temperature catalytic processes.