# A donor–acceptor zwitterion as a self-assembled hole-selective layer for highly efficient tin-based perovskite solar cells

**Authors:** Qianqian Chang, Guosen Zhang, Diwei Zhang, Peng Lin, Jingjing Li, Xurang Wang, Tianci Gu, Jingying Lin, Yuan Lin, Xiaozhen Li, Mingwei An, Yu Cao, Chengbo Tian, Yang Wang

PMC · DOI: 10.1039/d5sc08439c · Chemical Science · 2025-12-29

## TL;DR

A new zwitterionic molecule improves the efficiency and stability of tin-based perovskite solar cells.

## Contribution

A donor–acceptor zwitterion is introduced as a hole-selective layer for tin-based perovskite solar cells.

## Key findings

- PyPs-based devices achieved a record power conversion efficiency of 12.18%.
- Unencapsulated devices retained 90% efficiency after 1800 hours of storage.

## Abstract

The development of tin-based perovskite solar cells (TPSCs) has lagged far behind that of their lead-based counterparts. Although high-efficiency TPSCs have been reported in recent years, they are all based on poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) as the hole-selective layer (HSL), whose strong acidity and hygroscopicity are undoubtedly highly detrimental to the long-term stability of the devices. Here, a donor–acceptor-type zwitterionic molecule (PyPs) was designed by employing a triphenylamine donor and a benzo[c][1,2,5]thiadiazole acceptor as the molecular backbone, functionalized with a pyridinium sulfonate terminal group. The ionic sulfonate group in PyPs not only exhibits stronger coordination with indium tin oxide (ITO), enabling uniform surface coverage and improved energy-level alignment, but also assists the growth and defect passivation of a tin perovskite. As a result, high-quality Sn-based perovskite films can be obtained along with accelerated interfacial charge extraction and suppressed non-radiative recombination losses. Encouragingly, PyPs-based devices deliver a champion power conversion efficiency (PCE) of 12.18%, representing the highest efficiency reported to date for TPSCs based on alternative HSLs to PEDOT:PSS. Moreover, unencapsulated PyPs-based devices retain 90% of their initial PCE after 1800 h of storage. This work highlights the potential of rational molecular design in the exploration of alternative HSLs for efficient and stable TPSCs.

A donor–acceptor zwitterion, PyPs, has been proposed to regulate the crystallization kinetics and hole-selective contact in tin-based perovskite solar cells (TPSCs), achieving a record-breaking efficiency of 12.18%.

## Linked entities

- **Chemicals:** triphenylamine (PubChem CID 11775), benzo[c][1,2,5]thiadiazole (PubChem CID 67502), pyridinium sulfonate (PubChem CID 2777373), indium tin oxide (PubChem CID 16213631)

## Full-text entities

- **Chemicals:** perovskite (MESH:C059910), lead (MESH:D007854), Sn (MESH:D014001), poly(styrenesulfonate) (MESH:C003321), PEDOT:PSS (MESH:C533756), ITO (MESH:C109984), poly(3,4-ethylenedioxythiophene) (MESH:C121383), PyPs (-)

## Full text

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## Figures

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## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12805863/full.md

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Source: https://tomesphere.com/paper/PMC12805863