Passivation Mechanism of (18-Crown-6) Potassium on Complex Defects in SnO2 Electron Transport Layer of Solar Cells
In this study, first-principles calculations were employed to systematically investigate the interaction mechanisms between (18-crown-6) potassium (18C6-K<sup>+</sup>) and six typical defect sites on the SnO<sub>2</sub> (110) surface, including Sn<sub>i</sub> + Sn<sub>O</sub>, O<sub>i</sub> + O<sub>Sn</sub>, V<sub>O</sub> + Sn<sub>i</sub>, V<sub>Sn</sub> + Sn<sub>O</sub>, V<sub>Sn</sub> + Sn<sub>i</sub>, and Sn<sub>i</sub>. Six intrinsic or complex defects universally coexist on the SnO<sub>2</sub> surface, and the defect states they introduced allow for precise tuning of material performance. The results demonstrated that the 18C6-K<sup>+</sup> molecule can stably adsorb on all six defect sites and significantly increase defect formation energies, indicating its thermodynamic capability to suppress defect generation. A subsequent density of states (DOS) analysis revealed that the 18C6-K<sup>+</sup> molecule exhibits strong defect passivation effects at Sn<sub>i</sub> + Sn<sub>O</sub>, V<sub>O</sub> + Sn<sub>i</sub>, V<sub>Sn</sub> + Sn<sub>i</sub>, and Sn<sub>i</sub> sites, and partially mitigated the electronic disturbances induced by O<sub>i</sub> + O<sub>Sn</sub> and V<sub>Sn</sub> + Sn<sub>O</sub> defects. Furthermore, the incorporation of 18C6-K<sup>+</sup> has been shown to reduce the electronic effective mass of defective systems, thereby enhancing surface carrier transport. A subsequent charge density difference (CDD) analysis revealed that the 18C6-K<sup>+</sup> molecule forms Sn-ether and O-ether interactions through its ether bonds (C-O-C) with surface Sn and O atoms, inducing interfacial electronic reconstruction and charge transfer. The Bader charge analysis revealed that the H, C, and O atoms in 18C6-K<sup>+</sup> lose electrons, whereas the Sn or O atoms at the surface defect sites gain electrons. This outcome is consistent with the CDD analysis and quantitatively confirms the extent of electron transfer from 18C6-K<sup>+</sup> to the SnO<sub>2</sub> defect regions. These interactions effectively passivate defect states, thereby enhancing interfacial stability. The present study offers theoretical guidance and design insights for the development of molecular passivation strategies in SnO<sub>2</sub>-based optoelectronic devices.
Authors
- Xihua Zhang
- Longxian Zhang (ORCID: https://orcid.org/0000-0002-5706-131X)
- Yu Zhuang (ORCID: https://orcid.org/0000-0003-2717-1777)
- Qiaogang Song (ORCID: https://orcid.org/0000-0002-3786-9979)
- Xianfeng Jiang (ORCID: https://orcid.org/0000-0002-2187-9005)
- Shiyan Yang (ORCID: https://orcid.org/0000-0003-3017-3167)
- Jianjun Wang (ORCID: https://orcid.org/0000-0001-5732-1911)
- Hongwen Zhang (ORCID: https://orcid.org/0000-0002-1358-7336)
- Wenjing Lu
- Qiuli Zhang
- Xintong Zhao (ORCID: https://orcid.org/0000-0002-9892-6922)
- Shurong Wang
- Youbo Dou
Institutions
- Yunnan Normal University (CN)
Publication Details
- Journal
- Molecules
- Published
- 2025-10-14
- DOI
- https://doi.org/10.3390/molecules30204081
- Primary Topic
- Gas Sensing Nanomaterials and Sensors
- Type
- article
- Field-Weighted Citation Impact
- 0.00