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ACTA PHYSICO-CHIMICA SINICA · 2024 · IF 10.8

NbSe2 Nanosheets Improved the Buried Interface for Perovskite Solar Cells

Pengyu Dong,Yue Jiang,Zhengchi Yang,Licheng Liu,Gu Li,Xinyang Wen,Zhen Wang,Xinbo Shi,Guofu Zhou,Jun-Ming Liu,Jinwei Gao

Organic-inorganic metal halide perovskite solar cells (PSCs) are favorable candidates for next-generation solar cells, due to their excellent photovoltaic performance and promising low-cost fabrication process. Particularly, tin oxide (SnO 2 ), with excellent charge mobility and extraction efficiency, is widely used as electron transport layers (ETLs), and the efficiency of the corresponding n-i-p-type perovskites has been certified as high as 26.21% in single-junction devices. The SnO 2 layer serves as the substrate for the growth of perovskite films, determining the crystalline quality and the buried interface of perovskite films. However, due to the different thermal expansion coefficient of SnO 2 and perovskite, the subsequent perovskite annealing process leads to the residual stress at the buried interfaces and lattice distortion in the perovskite films, which seriously affects their optoelectronic performance and stability. To release this interfacial stress, researchers have made some progress by applying different polymers and small molecules to the SnO 2 /perovskite interface as a buffer layer. Among these, two-dimensional (2D) nanosheets with high carrier mobility, a wide bandgap range, and excellent optical absorption properties are promising, especially 2D NbSe 2 nanosheets showing the advantages of solution-processability, high intrinsic conductivity and clean smooth surface, namely without dangling bonded atoms. Herein, 2D NbSe 2 nanosheets have been introduced at the SnO 2 /perovskite interface to release the undesired residual tensile strain in perovskite films and to form a more matched interfacial energy level alignment. As a result, we have obtained a high-quality perovskite film and further an improved photovoltaic performance. The PCE has been increased from 21.81% to 24.05%. The unencapsulated cell maintained 91% of the initial efficiency after aging over 1000 h under atmospheric condition.

研究领域: 材料科学 · 能源技术 · 光伏器件
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Journal of Materials Chemistry B · 2019 ·Vol. 7 ·期 19 ·3134-3142 · IF 5.047

NIR light-responsive short peptide/2D NbSe2 nanosheets composite hydrogel with controlled-release capacity

Can Wu,Jing Liu,Bin Liu,Suyun He,Guoru Dai,Bo Xu,Wenying Zhong

The design of light-responsive peptide hydrogels with controllable drug release characteristics is still a challenge. Here, we fabricated a NIR light-responsive short peptide hydrogel by using a thermo-responsive short peptide hydrogel and PEGylated NbSe2 nanosheets, namely, the NbSe2–PEG@YD hydrogel. Under NIR light irradiation, the hydrogel began to collapse owing to the local heating, leading to the release of the cargos. The hydrogel exhibited recoverability and the release rate of the cargos could be accurately modulated by the NIR light irradiation according to the requirement. The excellent biocompatibility of this hydrogel ensured that it could be further developed as a drug carrier for clinical application.

研究领域: 生物材料 · 药剂学 · 纳米医学
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