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<p>Excited-state charge transfer underpins organic photovoltaics, photocatalysis and photodetection, but is traditionally thought to require large energy offsets and strong donor–acceptor coupling that can limit device performance. Here, we investigate through-space polymer non-fullerene-acceptor based model heterojunctions in which a perylene diimide acceptor is covalently tethered to a low-bandgap polymer donor. These systems feature an exceptionally small energy offset (&lt; 100 meV) between frontier orbitals, with weak donor–acceptor coupling in the Franck–Condon region. We nevertheless achieve a charge-transfer timescale of ~18 fs. This ultrafast charge-transfer is accompanied via the launch of coherent wavepackets along a high-frequency vibrational coordinate (26 fs period) on the non-fullerene acceptor’s potential energy surface. We uncover specific polymer-centered driving vibrational modes that enable such rapid charge-transfer rates, by mixing Frenkel exciton and charge-transfer states following photoexcitation. Our results demonstrate that ultrafast charge-transfer can be achieved—ultimately limited by high-frequency vibrational periods—even in the absence of large energy offsets or strong ground-state coupling.</p>

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Vibronically assisted sub-cycle charge transfer at a non-fullerene acceptor heterojunction

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年3月5日

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  • Pratyush Ghosh,
  • Jeroen Royakkers,
  • Giacomo Londi,
  • Samuele Giannini,
  • Rakesh Arul,
  • Alexander J. Gillett,
  • Scott T. Keene,
  • Szymon J. Zelewski,
  • David Beljonne,
  • Hugo Bronstein,
  • Akshay Rao

摘要

Excited-state charge transfer underpins organic photovoltaics, photocatalysis and photodetection, but is traditionally thought to require large energy offsets and strong donor–acceptor coupling that can limit device performance. Here, we investigate through-space polymer non-fullerene-acceptor based model heterojunctions in which a perylene diimide acceptor is covalently tethered to a low-bandgap polymer donor. These systems feature an exceptionally small energy offset (< 100 meV) between frontier orbitals, with weak donor–acceptor coupling in the Franck–Condon region. We nevertheless achieve a charge-transfer timescale of ~18 fs. This ultrafast charge-transfer is accompanied via the launch of coherent wavepackets along a high-frequency vibrational coordinate (26 fs period) on the non-fullerene acceptor’s potential energy surface. We uncover specific polymer-centered driving vibrational modes that enable such rapid charge-transfer rates, by mixing Frenkel exciton and charge-transfer states following photoexcitation. Our results demonstrate that ultrafast charge-transfer can be achieved—ultimately limited by high-frequency vibrational periods—even in the absence of large energy offsets or strong ground-state coupling.