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.

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Journal
Molecules
Published
2025-10-14
DOI
https://doi.org/10.3390/molecules30204081
Primary Topic
Gas Sensing Nanomaterials and Sensors
Type
article
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article

Passivation Mechanism of (18-Crown-6) Potassium on Complex Defects in SnO2 Electron Transport Layer of Solar Cells

Xihua Zhang, Longxian Zhang, Yu Zhuang, Qiaogang Song et al.
Molecules
Gas Sensing Nanomaterials and Sensors
article

Passivation Mechanism of (18-Crown-6) Potassium on Complex Defects in SnO2 Electron Transport Layer of Solar Cells

Xihua Zhang, Longxian Zhang, Yu Zhuang, Qiaogang Song, Xianfeng Jiang, Shiyan Yang, Jianjun Wang, Hongwen Zhang, Wenjing Lu, Qiuli Zhang, Xintong Zhao, Shurong Wang, Youbo Dou
article en

Abstract

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.

MoleculesVol. 30(20)
Yunnan Normal University (CN)
Openalex Percentile: Top 71%
Gas Sensing Nanomaterials and Sensors
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