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Enabling direct-growth route for highly efficient ethanol upgrading to long-chain alcohols in aqueous phase.

Juwen GuWanbing GongQian ZhangRan LongJun MaXinyu WangJiawei LiJiayi LiYujian FanXinqi ZhengSongbai QiuTiejun WangYujie Xiong
Published in: Nature communications (2023)
Upgrading ethanol to long-chain alcohols (LAS, C 6+ OH) offers an attractive and sustainable approach to carbon neutrality. Yet it remains a grand challenge to achieve efficient carbon chain propagation, particularly with noble metal-free catalysts in aqueous phase, toward LAS production. Here we report an unconventional but effective strategy for designing highly efficient catalysts for ethanol upgrading to LAS, in which Ni catalytic sites are controllably exposed on surface through sulfur modification. The optimal catalyst exhibits the performance well exceeding previous reports, achieving ultrahigh LAS selectivity (15.2% C 6 OH and 59.0% C 8+ OH) at nearly complete ethanol conversion (99.1%). Our in situ characterizations, together with theoretical simulation, reveal that the selectively exposed Ni sites which offer strong adsorption for aldehydes but are inert for side reactions can effectively stabilize and enrich aldehyde intermediates, dramatically improving direct-growth probability toward LAS production. This work opens a new paradigm for designing high-performance non-noble metal catalysts for upgrading aqueous EtOH to LAS.
Keyphrases
  • highly efficient
  • ionic liquid
  • genome wide
  • gene expression
  • transition metal