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Room-temperature electrochemical acetylene reduction to ethylene with high conversion and selectivity

  • Run Shi
  • , Zeping Wang
  • , Yunxuan Zhao
  • , Geoffrey I.N. Waterhouse
  • , Zhenhua Li
  • , Bikun Zhang
  • , Zhimei Sun
  • , Chuan Xia
  • , Haotian Wang*
  • , Tierui Zhang*
  • *Corresponding author for this work
  • CAS - Technical Institute of Physics and Chemistry
  • University of Chinese Academy of Sciences
  • The University of Auckland
  • Central China Normal University
  • Beihang University
  • Rice University

Research output: Contribution to journal › Article › peer-review

Abstract

The selective hydrogenation of acetylene to ethylene in ethylene-rich gas streams is an important process in the manufacture of polyethylene. Conventional thermal hydrogenation routes require temperatures above 100 °C and excess hydrogen to achieve a satisfactory C2H2 conversion efficiency. Here, we report a room-temperature electrochemical acetylene reduction system based on a layered double hydroxide (LDH)-derived copper catalyst that offers an ethylene Faradaic efficiency of up to ~80% and inhibits alkane and hydrogen formation. The system affords an acetylene conversion of over 99.9% at a flow rate of 50 ml min−1 in a simulated gas feed, yielding high-purity ethylene with an ethylene/acetylene volume ratio exceeding 105 and negligible residual hydrogen (0.08 vol.%). These acetylene conversion metrics are superior to most other state-of-the-art strategies. The findings therefore conclusively demonstrate an electrochemical strategy as a viable alternative to current technologies for acetylene-to-ethylene conversions with potential advantages in energy and atom economies. [Figure not available: see fulltext.].

Original languageEnglish
Pages (from-to)565-574
Number of pages10
JournalNature Catalysis
Volume4
Issue number7
DOIs
StatePublished - Jul 2021

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