4.8 Article

Rational tuning of intermolecular and intramolecular interactions enabling high-efficiency indoor organic photovoltaics

Journal

NANO ENERGY
Volume 99, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.nanoen.2022.107414

Keywords

Indoor organic photovoltaics; Intramolecular interaction; Intermolecular interaction; Trap state; Voltage loss; Flexible device

Funding

  1. National Science Fund for Distinguished Young Scholars [21925506]
  2. National Natural Science Foundation of China [U21A20331, 81903743, 22171153]
  3. CAS Key Project of Frontier Science Research [QYZDB-SSW-SYS030]
  4. Ningbo Natural Science Foundation [2021J192]
  5. Technology of the People's Republic of China under funding scheme National Key R&D Program of Intergovernmental Kay Projects [2018YFE0101700]
  6. Ningbo Science and Technology Bureau [2020Z092]

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This study adopts a new strategy to improve the power conversion efficiency of indoor organic photovoltaics (IOPVs) by tuning the molecular structure through changing the skeleton and end group. The research reveals that asymmetry and non-chlorination in the molecular structure can enhance the intra and intermolecular charge transfer, leading to higher performance. Under artificial light, the novel acceptor exhibits high-efficiency rigid and flexible PCE.
Indoor organic photovoltaics (IOPVs) are one of promising candidates for transferring artificial illumination to power the Internet of Things (IoT). However, their power conversion efficiencies (PCE) are limited by the fact that only a few efficient non-fullerene acceptors are available for IOPVs. Herein, new strategy is adopted to tune the intramolecular charge transfer (intra-CT) and intermolecular charge transfer (inter-CT) to achieve high PCEs under indoor environment in the combination of changing skeleton from symmetry to asymmetry and end group from chlorination to non-chlorination. The study reveals that, in comparison with symmetric molecule BTP-2ThCl, asymmetric structure TB-SCl possesses a smaller intra-CT resulting in higher V-OC and strengthened inter-CT for neighboring acceptors resulting in more efficient carrier collection and thus higher FF. Moreover, the non-chlorine molecule TB-S exhibits smaller intra and inter-CT leading to further promoting V-OC but smaller FF compared with TB-SCl under 1-sun illumination. When the illumination is switched to artificial light, the mitigated trap state, minimized leakage current, and suppressed non-radiative energy loss (Delta E-nonrad) enable a novel acceptor TB-S yielding high-efficiency rigid PCE of 23.3 % which surpasses TB-SCl and flexible PCE of 20.02% which is one of the best PCE for flexible IOPVs. Our observation provides a new insight into molecule structure modification to promote the indoor photovoltaic performance.

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