Carbon matrix anchored Rh1Co single-atom alloy catalyst for robust hydroformylation with wide substrate generality

  • Xin Zhang
  • , Xuelu Ma
  • , Hsiao Chien Chen
  • , Shu Tao
  • , Da Yang
  • , Yingying Liu
  • , Wenwen Gao
  • , Guangxun Sun
  • , Tingyu Chang
  • , Zhidong Wang
  • , Bin Liu
  • , Yongming Chai
  • , Zhi Liu
  • , Yuan Pan*
  • *Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

2 Scopus citations

Abstract

A novel Rh1Co single-atom alloy (SAA) catalyst, in which Rh species are atomically dispersed on Co nanoparticles that are anchored by N-doped carbon (N-C) matrix for hydroformylation of olefins. The Rh1Co SAA/N-C catalyst exhibits high activity towards the hydroformylation of 1-hexene, achieving both nearly 100% conversion and selectivity as well as good cycle stability. It also shows extremely wide substrate generality for at least 17 different types of olefins. A synergistic catalytic mechanism of the Rh1Co SAA/N-C catalyst was discovered that H2 is dissociated on Co sites and Co-H species are facilitated to be generated, CO is also adsorbed and inserted on Co sites that promote the C-C coupling, while the Rh-Co dual sites are beneficial to the co-adsorption of 1-hexene. Theoretical calculations reveal the Rh1Co SAA/N-C catalyst shows a lower rate-determining energy barrier of CO insertion due to the optimized charge distribution of the precursor of CO insertion at Co sites.

Original languageEnglish
Article numbere18798
JournalAIChE Journal
Volume71
Issue number6
DOIs
StatePublished - 06 2025

Bibliographical note

Publisher Copyright:
© 2025 American Institute of Chemical Engineers.

Keywords

  • heterogeneous catalyst
  • hydroformylation
  • single-atom alloy catalyst
  • synergistic mechanism

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