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Hydroboration-Oxidation of Alkenes03:08

Hydroboration-Oxidation of Alkenes

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In addition to the oxymercuration–demercuration method, which converts the alkenes to alcohols with Markovnikov orientation, a complementary hydroboration-oxidation method yields the anti-Markovnikov product. The hydroboration reaction, discovered in 1959 by H.C. Brown, involves the addition of a B–H bond of borane to an alkene giving an organoborane intermediate. The oxidation of this intermediate with basic hydrogen peroxide forms an alcohol.
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The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
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In a galvanic cell, the electrical work is done by a redox system on its surroundings as electrons produced by the spontaneous redox reactions are transferred through an external circuit. Alternatively, an external circuit does work on a redox system by imposing a voltage sufficient to drive an otherwise nonspontaneous reaction in a process known as electrolysis. For instance, recharging a battery involves the use of an external power source to drive the spontaneous (discharge) cell reaction in...
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Assessment of Boron Doped Diamond Electrode Quality and Application to In Situ Modification of Local pH by Water Electrolysis
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Alkaline Water Oxidation Using a Bimetallic Phospho-Boride Electrocatalyst.

Avani Chunduri1, Suraj Gupta2, Maulik Patel2

  • 1Department of Physics, University of Mumbai Vidyanagari, Santacruz (East), Mumbai, 400098, India.

Chemsuschem
|October 28, 2020
PubMed
Summary

Developing new electrocatalysts for oxygen evolution reaction (OER) is crucial for global water electrolysis. This study introduces a low-cost bimetallic catalyst with record-breaking OER activity, paving the way for efficient hydrogen production.

Keywords:
alkaline water oxidationlow-cost electrocatalystsmass activitymetal phospho-boridesoxygen evolution reaction

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Catalysis

Background:

  • Global application of water electrolysis necessitates highly active, low-cost electrocatalysts for the oxygen evolution reaction (OER).
  • Existing OER catalysts often rely on expensive noble metals, limiting large-scale implementation.

Purpose of the Study:

  • To develop a novel, cost-effective bimetallic catalyst for enhanced OER performance in alkaline water electrolysis.
  • To investigate the synergistic effects of phospho-boride composition and molybdenum doping on catalytic activity.

Main Methods:

  • Synthesis of a bimetallic phospho-boride catalyst with controlled composition.
  • Electrochemical characterization of the catalyst's OER activity in alkaline media.
  • Analysis of catalyst structure and electronic properties to understand performance enhancement.

Main Results:

  • The developed catalyst achieved an OER activity of ~195 mV to reach 10 mA cm⁻² at a low loading of 0.3 mg cm⁻².
  • The bimetallic structure modulated cobalt electron density, forming highly active CoOOH species.
  • Molybdenum addition further boosted activity by increasing surface area and forming nano-crystalline domains, achieving a benchmark mass activity of 666 A g⁻¹ at 300 mV.

Conclusions:

  • The novel bimetallic phospho-boride catalyst demonstrates exceptional OER performance, setting a new benchmark for low-cost electrocatalysts.
  • This work offers a promising strategy for fabricating advanced electrode materials for efficient water electrolysis and sustainable hydrogen production.