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