Perovskite Quantum Dot Solar Cells with 15.6% Efficiency and Improved Stability Enabled by an α-CsPbI3/FAPbI3 Bilayer Structure AITranslate
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We developed lead halide perovskite quantum dot (QD) solar cells with a combinational absorbing layer based on stacked α-CsPbI3 and FAPbI3. α-CsPbI3 QDs, with a relatively wide bandgap of 1.75 eV, are not ideal for single-junction solar cells. We show that the absorption can be broadened by the introduction of another QD layer with a narrower bandgap like FAPbI3. The α-CsPbI3/FAPbI3 structure together with thermal annealing can improve the electrical coupling in the FAPbI3 layer and induce A-site cation exchange to develop a graded heterojunction for more efficient charge extraction. A highest power conversion efficiency of 15.6% and improved ambient stability have been achieved for the bilayer structured solar cells. More interestingly, the perovskite QDs provided a facile way to fabricate multiple layers and quantum junctions for optoelectronic applications via layer-by-layer deposition, which cannot be realized in solution-processed perovskite thin-film devices.
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DOI:https://doi.org/10.1021/acsenergylett.9b01920
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We developed lead halide perovskite quantum dot (QD) solar cells with a combinational absorbing layer based on stacked α-CsPbI3 and FAPbI3. α-CsPbI3 QDs, with a relatively wide bandgap of 1.75 eV, are not ideal for single-junction solar cells. We show that the absorption can be broadened by the introduction of another QD layer with a narrower bandgap like FAPbI3. The α-CsPbI3/FAPbI3 structure together with thermal annealing can improve the electrical coupling in the FAPbI3 layer and induce A-site cation exchange to develop a graded heterojunction for more efficient charge extraction. A highest power conversion efficiency of 15.6% and improved ambient stability have been achieved for the bilayer structured solar cells. More interestingly, the perovskite QDs provided a facile way to fabricate multiple layers and quantum junctions for optoelectronic applications via layer-by-layer deposition, which cannot be realized in solution-processed perovskite thin-film devices.
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| GB/T 7714-2015 | [1] Fangchao Li, Sijie Zhou, Jianyu Yuan, et al. ACS Energy Letters, 2019(4). DOI:10.1021/acsenergylett.9b01920. |
| MLA | [1] Fangchao Li, et al., ACS Energy Letters, no. 4, 2019, https://doi.org/10.1021/acsenergylett.9b01920. |
| APA | [1] Fangchao Li, Sijie Zhou, Jianyu Yuan, Chaochao Qin, Yingguo Yang, Junwei Shi, Xufeng Ling, Youyong Li, & Wanli Ma. (2019). ACS Energy Letters(4). https://doi.org/10.1021/acsenergylett.9b01920 |
| IEEE | [1] Fangchao Li, Sijie Zhou, Jianyu Yuan, Chaochao Qin, Yingguo Yang, Junwei Shi, Xufeng Ling, Youyong Li, and Wanli Ma, ACS Energy Letters, no. 4, 2019, doi: 10.1021/acsenergylett.9b01920. |
