Nature Communications (Jan 2025)

Pt/IrO x enables selective electrochemical C-H chlorination at high current

  • Bo Wu,
  • Ruihu Lu,
  • Chao Wu,
  • Tenghui Yuan,
  • Bin Liu,
  • Xi Wang,
  • Chenyi Fang,
  • Ziyu Mi,
  • Surani Bin Dolmanan,
  • Weng Weei Tjiu,
  • Mingsheng Zhang,
  • Bingqing Wang,
  • Zainul Aabdin,
  • Sui Zhang,
  • Yi Hou,
  • Bote Zhao,
  • Shibo Xi,
  • Wan Ru Leow,
  • Ziyun Wang,
  • Yanwei Lum

DOI
https://doi.org/10.1038/s41467-024-55283-x
Journal volume & issue
Vol. 16, no. 1
pp. 1 – 15

Abstract

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Abstract Employing electrochemistry for the selective functionalization of liquid alkanes allows for sustainable and efficient production of high-value chemicals. However, the large potentials required for C(sp 3)-H bond functionalization and low water solubility of such alkanes make it challenging. Here we discover that a Pt/IrO x electrocatalyst with optimized Cl binding energy enables selective generation of Cl free radicals for C-H chlorination of alkanes. For instance, we achieve monochlorination of cyclohexane with a current up to 5 A, Faradaic efficiency (FE) up to 95% and stable performance over 100 h in aqueous KCl electrolyte. We further demonstrate that our system can directly utilize concentrated seawater derived from a solar evaporation reverse osmosis process, achieving a FE of 93.8% towards chlorocyclohexane at a current of 1 A. By coupling to a photovoltaic module, we showcase solar-driven production of chlorocyclohexane using concentrated seawater in a membrane electrode assembly cell without any external bias. Our findings constitute a sustainable pathway towards renewable energy driven chemicals manufacture using abundant feedstock at industrially relevant rates.