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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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Oxidation-reduction or redox reactions involve the transfer of electrons from one molecule or atom to another. When an atom gains an electron, another atom must lose an electron, meaning oxidation and reduction must occur together. Since the redox occurs in pairs, the atom that gets oxidized is also called the reducing agent or reductant, and the atom that is reduced is also called the oxidizing agent or oxidant. A straightforward way to remember the definitions of oxidation and reduction is...
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In the presence of organic peroxides, the addition of hydrogen bromide to an alkene yields the isomer that is not predicted by Markovnikov’s rule. For example, the addition of hydrogen bromide to 2-methylpropene in the presence of peroxides gives 1-bromo-2-methylpropane. This addition reaction proceeds via a free radical mechanism, which reverses the regioselectivity. The free radical reaction mechanism involves three stages: initiation, propagation, and termination.
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Updated: Jun 30, 2025

Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase
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Electron Spin Selective Iridium Electrocatalysts for the Oxygen Evolution Reaction.

Carlos J Mingoes1, Bob C Schroeder2, Ana B Jorge Sobrido1

  • 1School of Engineering and Materials Science, Queen Mary University of London, Mile End Road, London E1 4NS, U.K.

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|March 18, 2024
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Summary

Chiral molecule functionalization significantly boosts iridium nanoparticle electrocatalyst activity for oxygen evolution reaction (OER) in water electrolysis. This enhances sustainable energy technologies by improving efficiency and reducing byproducts.

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Sustainable Energy

Background:

  • Efficient electrocatalysts are vital for water electrolysis and a sustainable energy future.
  • Iridium-based materials are well-known electrocatalysts, but their activity requires enhancement for commercial viability.

Purpose of the Study:

  • To investigate a novel method for enhancing the electrocatalytic activity of iridium nanoparticles for the oxygen evolution reaction (OER).
  • To explore the impact of chiral molecule functionalization on iridium nanoparticle performance in water electrolysis.

Main Methods:

  • Synthesis of iridium nanoparticles (2.1 ± 0.2 nm) functionalized with chiral molecules.
  • Comparative electrochemical testing of chiral-functionalized, achiral-functionalized, and unfunctionalized iridium nanoparticles.
  • Measurement of OER activity at a potential of 1.55 V vs. Reference Hydrogen Electrode (RHE).
  • Colorimetric analysis to detect hydrogen peroxide production.

Main Results:

  • Chiral-functionalized iridium nanoparticles demonstrated a significant enhancement in OER activity (average 85% increase) compared to unfunctionalized nanoparticles.
  • Achiral-functionalized nanoparticles showed a modest activity enhancement (average 13%).
  • The enhanced activity is attributed to a spin-selective electron transfer mechanism induced by the ligand's chirality.
  • Chiral functionalization drastically reduced hydrogen peroxide production.

Conclusions:

  • Chiral molecule functionalization is a highly effective strategy for boosting the OER activity of iridium electrocatalysts.
  • The observed enhancement is linked to chirality-induced spin-selective electron transfer.
  • This approach offers a promising pathway for developing advanced electrocatalysts for efficient and sustainable water electrolysis.