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2D Intermediate Suppression for Efficient Ruddlesden–Popper (RP) Phase Lead-Free Perovskite Solar Cells AITranslate

Nanjing Tech University (NanjingTech); Nanjing Tech University (NanjingTech); Nanjing Tech University (NanjingTech); Nanjing Tech University (NanjingTech); Nanjing Tech University (NanjingTech); Nanjing Tech University (NanjingTech); Nanjing Tech University (NanjingTech); Nanjing Tech University (NanjingTech); Nanjing Tech University (NanjingTech); Shanghai Institute of Applied Physics; Shanghai Institute of Applied Physics; Northwestern Polytechnical University (NPU); Nanjing University of Posts and Telecommunications
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Publisher: ACS
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Abstract AITranslate

2D Ruddlesden–Popper (2DRP) tin (Sn) perovskite solar cells (PSCs) play an irreplaceable role in advancing the commercialization of perovskite-based photovoltaic devices due to their low toxicity and improved stability. However, the efficiency of 2DRP Sn PSCs has not made a breakthrough owing to incompletely oriented crystal growth and poor film morphology, which is limited by a complex and uncontrollable crystallization process. Here, we first introduce the mixed spacer organic cations [n-butylamine (BA) and phenylethylamine (PEA)] in 2DRP Sn perovskite to control the crystallization process. We find that when the BA+ and PEA+ co-work to form [(BA0.5PEA0.5)2FA3Sn4I13] 2DRP perovskites, the intermediate phase impeding the homogeneous and ordered nucleation of the crystal is suppressed effectively, thus enabling a high-quality film morphology and improved crystal orientation. Benefitting from it, the power conversion efficiency (PCE) is improved to 8.82%, which is the highest one among the 2DRP Sn PSCs as far as we known.

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DOI:https://doi.org/10.1021/acsenergylett.9b00954

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Citation Information:

2D Ruddlesden–Popper (2DRP) tin (Sn) perovskite solar cells (PSCs) play an irreplaceable role in advancing the commercialization of perovskite-based photovoltaic devices due to their low toxicity and improved stability. However, the efficiency of 2DRP Sn PSCs has not made a breakthrough owing to incompletely oriented crystal growth and poor film morphology, which is limited by a complex and uncontrollable crystallization process. Here, we first introduce the mixed spacer organic cations [n-butylamine (BA) and phenylethylamine (PEA)] in 2DRP Sn perovskite to control the crystallization process. We find that when the BA+ and PEA+ co-work to form [(BA0.5PEA0.5)2FA3Sn4I13] 2DRP perovskites, the intermediate phase impeding the homogeneous and ordered nucleation of the crystal is suppressed effectively, thus enabling a high-quality film morphology and improved crystal orientation. Benefitting from it, the power conversion efficiency (PCE) is improved to 8.82%, which is the highest one among the 2DRP Sn PSCs as far as we known.

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GB/T 7714-2015 [1] Jian Qiu, Yingdong Xia, Yiting Zheng, et al. ACS Energy Letters, 2019(4). DOI:10.1021/acsenergylett.9b00954.
MLA [1] Jian Qiu, et al., ACS Energy Letters, no. 4, 2019, https://doi.org/10.1021/acsenergylett.9b00954.
APA [1] Jian Qiu, Yingdong Xia, Yiting Zheng, Wei Hui, Hao Gu, Wenbo Yuan, Hui Yu, Lingfeng Chao, Tingting Niu, Yingguo Yang, Xingyu Gao, Yonghua Chen, & Wei Huang. (2019). ACS Energy Letters(4). https://doi.org/10.1021/acsenergylett.9b00954
IEEE [1] Jian Qiu, Yingdong Xia, Yiting Zheng, Wei Hui, Hao Gu, Wenbo Yuan, Hui Yu, Lingfeng Chao, Tingting Niu, Yingguo Yang, Xingyu Gao, Yonghua Chen, and Wei Huang, ACS Energy Letters, no. 4, 2019, doi: 10.1021/acsenergylett.9b00954.