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抑制缺陷诱导的α到δ相变以实现高效稳定的甲脒基钙钛矿太阳能电池

Inhibition of defect-induced α-to-δ phase transition for efficient and stable formamidinium perovskite solar cells.

作者信息

Chen Tian, Xie Jiangsheng, Wen Bin, Yin Qixin, Lin Ruohao, Zhu Shengcai, Gao Pingqi

机构信息

School of Materials, Shenzhen Campus of Sun Yat-sen University, No. 66, Gongchang Road, Shenzhen, Guangdong, 518107, PR China.

Institute for Solar Energy Systems, State Key Laboratory of Optoelectronic Materials and Technologies, Sun Yat-sen University, Guangzhou, 510275, PR China.

出版信息

Nat Commun. 2023 Sep 30;14(1):6125. doi: 10.1038/s41467-023-41853-y.

Abstract

Defects passivation is widely devoted to improving the performance of formamidinium lead triiodide perovskite solar cells; however, the effect of various defects on the α-phase stability is still unclear. Here, using density functional theory, we first reveal the degradation pathway of the formamidinium lead triiodide perovskite from α to δ phase and investigate the effect of various defects on the energy barrier of phase transition. The simulation results predict that iodine vacancies are most likely to trigger the degradation, since they obviously reduce the energy barrier of α-to-δ phase transition and have the lowest formation energies at the perovskite surface. A water-insoluble lead oxalate compact layer is introduced on the perovskite surface to largely suppress the α-phase collapse through hindering the iodine migration and volatilization. Furthermore, this strategy largely reduces the interfacial nonradiative recombination and boosts the efficiency of the solar cells to 25.39% (certified 24.92%). Unpackaged device can maintain 92% of its initial efficiency after operation at maximum power point under simulated air mass 1.5 G irradiation for 550 h.

摘要

缺陷钝化被广泛用于提高甲脒铅三碘化物钙钛矿太阳能电池的性能;然而,各种缺陷对α相稳定性的影响仍不清楚。在此,我们使用密度泛函理论,首先揭示了甲脒铅三碘化物钙钛矿从α相到δ相的降解途径,并研究了各种缺陷对相变能垒的影响。模拟结果预测碘空位最有可能引发降解,因为它们明显降低了α到δ相变的能垒,并且在钙钛矿表面具有最低的形成能。在钙钛矿表面引入一层水不溶性草酸铅致密层,通过阻碍碘的迁移和挥发,在很大程度上抑制α相的崩塌。此外,该策略大大降低了界面非辐射复合,并将太阳能电池的效率提高到25.39%(认证效率为24.92%)。在模拟空气质量1.5 G光照下最大功率点运行550 h后,未封装的器件可保持其初始效率的92%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17a0/10543379/17317b742980/41467_2023_41853_Fig1_HTML.jpg

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