Deep learning drives autonomous molecular reactions with single-bond selectivity in tetra-brominated porphyrins on Au(111)
The pursuit of autonomous chemical transformations with single-bond precision represents a central challenge in molecular nanoscience. While scanning tunneling microscopy (STM) enables site-specific reactions by directly engaging individual atoms and bonds, conventional approaches rely on expert intervention and lack reproducibility and scalability. Here we introduce a deep learning-based strategy that autonomously executes multi-step, bond-selective transformations. Our system integrates computer vision for molecular recognition, neural networks for bond-state classification, and deep reinforcement learning for closed-loop optimization of activation parameters. As a proof of concept, we demonstrate the selective dissociation of C-Br bonds in a tetra-brominated porphyrin on Au(111). Importantly, the approach extends beyond single-bond events, enabling programmed multi-step sequences including four distinct pathways with high fidelity. By advancing from isolated, human-directed manipulations to fully autonomous, data-driven reaction control, this platform establishes a paradigm for intelligent single-molecule chemistry. It provides a generalizable framework for on-surface synthesis, where adaptive agents orchestrate molecular transformations with a level of precision and scalability unattainable by manual approaches.
Authors
- Qiang Sun (ORCID: https://orcid.org/0000-0003-4903-4570)
- Tairan Yang (ORCID: https://orcid.org/0000-0002-7619-8696)
- Qi Huang (ORCID: https://orcid.org/0009-0002-7302-329X)
- Zhiwen Zhu (ORCID: https://orcid.org/0000-0002-6282-7463)
- Juan Xiang (ORCID: https://orcid.org/0000-0001-9492-7066)
- Liangliang Cai
- Shaoxuan Yuan
- Hao Jiang
Institutions
- Shanghai Research Institute of Materials (CN)
Publication Details
- Journal
- Nature Communications
- Published
- 2026-02-04
- DOI
- https://doi.org/10.1038/s41467-026-69080-1
- Primary Topic
- Surface Chemistry and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China