Highly Selective Hydrogen Peroxide Electrosynthesis on Carbon: In Situ Interface Engineering with Surfactants
By Kuang‐Hsu Wu, Dan Wang, Xingyu Lu, Xuefei Zhang, Zailai Xie, Yuefeng Liu, Bing-Jian Su, Jin‐Ming Chen, D. Su, W. Qi and 1 more. Chem, 2020
190 citations recorded by the source corpus.
Summary In situ modulation of surface reaction is a powerful approach to drive high-yield H2O2 electrosynthesis on metal-free carbon. Here, we discover that cationic surfactants can work efficiently as an in situ kinetic promoter for the oxygen-to-peroxide reaction on a carbon black electrode, achieving a peroxide yield above 90% (up to 95.2%) across a >0.8 V window in alkaline media, the best among reported H2O2 electrocatalysts. Our characterizations and kinetic model analysis show that the high peroxide selectivity is attributable to surface carboxylates (–COO−) with weak peroxide binding under a Coulombic pull imposed by an adsorbed cationic layer. Although surface carbonyls (–C=O) also participate in the peroxide synthesis, they exhibit strong binding to peroxide and promote on-site reduction at moderate-to-high overpotential. At only a minute amount of cationic surfactant, a chronoamperometry experiment with a carbonyl-free system can deliver a peroxide production at a sustainably high selectivity (∼96%) over 10 h.
Subfields: Electrical and Electronic Engineering, Electrochemistry, Renewable Energy, Sustainability and the Environment
View Paper: https://www.semanticscholar.org/paper/a1407627261b386baa994842664cb8bd63736aab
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In Electrical and Electronic Engineering
In Renewable Energy, Sustainability and the Environment
Citations in the corpus
- Insights into Practical-Scale Electrochemical H2O2 Synthesis (2020, background): “The surface carbonyl group (–C=O) also participates in peroxide synthesis, but it has stronger binding with peroxide, thus prohibiting peroxide desorption at higher overpotentials [56].”