Nature Communications (Jul 2024)

Light-driven C–H activation mediated by 2D transition metal dichalcogenides

  • Jingang Li,
  • Di Zhang,
  • Zhongyuan Guo,
  • Zhihan Chen,
  • Xi Jiang,
  • Jonathan M. Larson,
  • Haoyue Zhu,
  • Tianyi Zhang,
  • Yuqian Gu,
  • Brian W. Blankenship,
  • Min Chen,
  • Zilong Wu,
  • Suichu Huang,
  • Robert Kostecki,
  • Andrew M. Minor,
  • Costas P. Grigoropoulos,
  • Deji Akinwande,
  • Mauricio Terrones,
  • Joan M. Redwing,
  • Hao Li,
  • Yuebing Zheng

DOI
https://doi.org/10.1038/s41467-024-49783-z
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 7

Abstract

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Abstract C–H bond activation enables the facile synthesis of new chemicals. While C–H activation in short-chain alkanes has been widely investigated, it remains largely unexplored for long-chain organic molecules. Here, we report light-driven C–H activation in complex organic materials mediated by 2D transition metal dichalcogenides (TMDCs) and the resultant solid-state synthesis of luminescent carbon dots in a spatially-resolved fashion. We unravel the efficient H adsorption and a lowered energy barrier of C–C coupling mediated by 2D TMDCs to promote C–H activation and carbon dots synthesis. Our results shed light on 2D materials for C–H activation in organic compounds for applications in organic chemistry, environmental remediation, and photonic materials.