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Ultrahigh Density Array of Vertically Aligned Small-molecular Organic Nanowires on Arbitrary Substrates
Published on: June 18, 2013
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Ultra-narrow donor-acceptor nanoribbons
James Lawrence1,2, Luka Đorđević3,4, Fabienne Bachtiger5,6
1Department of Chemistry, University of Warwick, Coventry, UK. jmlaw91@nus.edu.sg.
Nature Communications
|April 23, 2026
Summary
Researchers synthesized ultra-narrow donor-acceptor nanoribbons on surfaces. This new method precisely controls the composition and electronic properties of these π-conjugated nanostructures for advanced optoelectronics.
Area of Science:
- Materials Science
- Organic Electronics
- Nanotechnology
Background:
- Donor-acceptor (D-A) architectures are crucial for high-performance conjugated polymers.
- Their application in atomically precise nanoribbons is largely unexplored.
Purpose of the Study:
- To report the on-surface synthesis of ultra-narrow D-A nanoribbons.
- To explore their structural and electronic properties.
- To establish a platform for engineering π-conjugated nanostructures.
Main Methods:
- On-surface synthesis using complementary brominated precursors (donor: peri-xanthenoxanthene, acceptor: anthanthrone).
- High-resolution scanning tunnelling microscopy (STM), non-contact atomic force microscopy (AFM), and scanning tunnelling spectroscopy (STS).
- Gas-phase density functional theory (DFT) calculations and a linear combination of molecular orbitals (LCAO) model.
Main Results:
- Successful synthesis of well-defined donor-only, acceptor-only, and mixed D-A nanoribbons.
- Submolecular structural and electronic features were resolved.
- Electronic properties were tuneable by monomer sequence and length.
- Experimental results align with DFT and LCAO models.
Conclusions:
- A bottom-up synthetic strategy provides precise control over nanoribbon composition and functionality.
- This approach enables the engineering of π-conjugated nanostructures with tailored optoelectronic properties.
- Opens new avenues for designing advanced organic electronic materials.

