| Literature DB >> 33511019 |
Long Hu1,2, Qi Lei1, Xinwei Guan1, Robert Patterson3, Jianyu Yuan4, Chun-Ho Lin1, Jiyun Kim1, Xun Geng1, Adnan Younis1, Xianxin Wu5, Xinfeng Liu5, Tao Wan1, Dewei Chu1, Tom Wu1, Shujuan Huang2,3.
Abstract
The surface chemistry of colloidal quantum dots (CQD) play a crucial role in fabricating highly efficient and stable solar cells. However, as-synthesized PbS CQDs are significantly off-stoichiometric and contain inhomogeneously distributed S and Pb atoms at the surface, which results in undercharged Pb atoms, dangling bonds of S atoms and uncapped sites, thus causing surface trap states. Moreover, conventional ligand exchange processes cannot efficiently eliminate these undesired atom configurations and defect sites. Here, potassium triiodide (KI3) additives are combined with conventional PbX2 matrix ligands to simultaneously eliminate the undercharged Pb species and dangling S sites via reacting with molecular I2 generated from the reversible reaction KI3 ⇌ I2 + KI. Meanwhile, high surface coverage shells on PbS CQDs are built via PbX2 and KI ligands. The implementation of KI3 additives remarkably suppresses the surface trap states and enhances the device stability due to the surface chemistry optimization. The resultant solar cells achieve the best power convention efficiency of 12.1% and retain 94% of its initial efficiency under 20 h continuous operation in air, while the control devices with KI additive deliver an efficiency of 11.0% and retains 87% of their initial efficiency under the same conditions.Entities:
Keywords: PbS colloidal quantum dots; chemical binding; solar cells; surface chemistry
Year: 2020 PMID: 33511019 PMCID: PMC7816699 DOI: 10.1002/advs.202003138
Source DB: PubMed Journal: Adv Sci (Weinh) ISSN: 2198-3844 Impact factor: 16.806