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苯基硫脲调控CsPbIBr2钙钛矿结晶及其光电性能

王桂强 王东升 毕佳宇 常嘉润 孟凡宁

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苯基硫脲调控CsPbIBr2钙钛矿结晶及其光电性能

王桂强, 王东升, 毕佳宇, 常嘉润, 孟凡宁

Tailoring of CsPbIBr2 perovskite crystallization via phenylthiourea for stable and efficiency perovskite solar cells

Wang Gui-Qiang, Wang Dong-Sheng, Bi Jia-Yu, Chang Jia-Run, Meng Fan-Ning
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  • 无机CsPbIBr2钙钛矿具有较高的稳定性和适合的带隙, 因此是一种较有应用前景的太阳能电池光吸收材料. 高质量的CsPbIBr2钙钛矿膜是组装高性能CsPbIBr2钙钛矿太阳能电池的关键. 本文通过在CsPbIBr2前驱体中加入苯基硫脲(PTU)调控前驱体反应结晶过程, 制备高质量的CsPbIBr2钙钛矿膜. 由于PTU与CsPbIBr2前驱体组分间存在较强的相互作用, 因此加入PTU导致在前驱体中形成PTU·Pb···Br(I)中间相. PTU·Pb···Br(I)中间相能够降低CsPbIBr2钙钛矿成核速率, 调控结晶生长过程, 从而制备了晶粒尺寸大、结晶度高、缺陷少的高质量CsPbIBr2钙钛矿膜. 同时, 前驱体热处理结晶过程中, PTU分解使S2–嵌入CsPbIBr2钙钛矿晶格, 显著提高了CsPbIBr2钙钛矿的稳定性. 本文所组装的碳基钙钛矿太阳能电池光电转换效率达到10.09%. 未密封电池在空气环境中贮存35 d, 效率仍能保持初始值的82%, 表明具有较高的稳定性.
    Inorganic CsPbIBr2 perovskite has been considered as a promising light-absorbing material for solar cells due to its high stability and suitable bandgap. Although the remarkable improvement of CsPbIBr2 PSC has been achieved, the efficiency of this cell is still lower than those of other analogues and far below its theoretical limit. This is mainly due to the serious charge recombination in the as-fabricated CsPbIBr2 cells derived from the poor-quality CsPbIBr2 perovskite film with a large quantity of defects and numerous grain boundaries. Therefore, fabricating high-quality CsPbIBr2 perovskite film is a key factor for the further efficiency improvement of CsPbIBr2 PSCs. Herein, phenylthiourea (PTU) additive is introduced into the CsPbIBr2 precursor to tailor the crystallization of CsPbIBr2 perovskite for fabricating high-quality CsPbIBr2 perovskite. The C=S group of PTU can coordinate with PbBr2 in the precursor owing to the lone-pair electrons on S and the empty orbits of Pb2+. The strong interaction between PTU and the CsPbIBr2 precursor components can form PTU·Pb···Br(I) intermediate phase in the precursor upon PTU introduction. The PTU·Pb···Br(I) intermediate phase can reduce the nucleation rate of perovskite and modulate the perovskite crystal growth because the extra energy is required to break the strong coordination bond in the intermediate phase, resulting in a low crystallization rate of CsPbIBr2 perovskite. Such a retardation of perovskite crystallization is conducive to the formation of high-crystallinity perovskite film with smooth surface, large crystal grains, high crystallization, and low density of defect. Meanwhile, the decomposition of PTU during thermal annealing makes the S2– inserted into interstitial of CsPbIBr2 crystal lattice, which greatly enhance the stability of CsPbIBr2 perovskite. The carbon-based PSCs with a normal n-i-p structure of FTO/compact-TiO2 layer/meso-TiO2 layer/perovskite film/carbon layer are fabricated, and their photovoltaic performances are measured under a simulated AM1.5 illumination (100 mW·cm–2). The PSC based on PTU-CsPbIBr2 perovskite delivers a high power conversion efficiency of 10.09%, which is much higher than that of the control device. This great improvement of photovoltaic performance can be attributed to the largely promoted perovskite quality, which enhances the charge collection and suppresses the charge recombination in the device. In addition, the unencapsulated device preserves 82% of the initial efficiency after being stored under ambient condition for 35 days, suggesting excellent stability. Therefore, this work provides an effective complementary strategy for effectively improving the performance of inorganic PSCs.
      通信作者: 王桂强, wgqiang@bhu.edu.cn ; 孟凡宁, mfn@qymail.bhu.edu.cn
    • 基金项目: 国家自然科学基金(批准号: 21805181)和辽宁教育厅重点项目(批准号: LZ2019003)资助的课题.
      Corresponding author: Wang Gui-Qiang, wgqiang@bhu.edu.cn ; Meng Fan-Ning, mfn@qymail.bhu.edu.cn
    • Funds: Project supported by the National Natural Science Foundation of China (Grant No. 21805181) and the Key Program of Education Department of Liaoning Province, China (Grant No. LZ2019003)
    [1]

    Jia X, Zou C T, Tao S X, Sun K. Zhao Y X, Yang S F, Chen M, Wang M K, Yuan Y B, Gao F, Wei Z H, Zhang L J, Yip H, Liu M Z, Shen Q, Yin L W, Tan H R, Jin Z W, Ding L M 2019 Sci. Bull. 64 1532Google Scholar

    [2]

    Tai Q, Tang K C, Yan F 2019 Energy Environ. Sci. 12 2375Google Scholar

    [3]

    Li B, Fu L, Li S, Chang B H, Li H, Yin L W 2019 J. Mater. Chem. A 7 20494Google Scholar

    [4]

    Faheem M B, Khan B, Feng C, Raziq F, Li Y B, Yao Y Q 2020 ACS Energy Lett. 5 290Google Scholar

    [5]

    Xiang W C, Tress W 2019 Adv. Mater. 31 1902851Google Scholar

    [6]

    Du Y C, Tian Q W, Chang X M, Fan J J, He X L, Ren X D, Zhao K, Liu S Z 2022 Adv. Mater. 34 2106750Google Scholar

    [7]

    Yu B C, Shi J J, Tan S, Zhao W Y, Hu H J, Luo Y H, Li D M, Meng Q B 2021 Angew. Chem. Int. Ed. 60 13436Google Scholar

    [8]

    Yoon S M, Min H, Kim J B, Lee S K, Seok S I 2021 Joule 5 183Google Scholar

    [9]

    Duan J L, Zhao Y Y, Yang X Y, Wang Y D, He B L, Tang Q W 2018 Adv. Energy Mater. 8 1802386Google Scholar

    [10]

    马书鹏, 林飞宇, 罗媛, 朱刘, 郭学益, 杨英 2022 物理学报 71 158101Google Scholar

    Ma S P, Lin F Y, Luo Y, Zhu L, Guo X Y, Yang Y 2022 Acta Phys. Sin. 71 158101Google Scholar

    [11]

    Montecucco R, Quadrivi E, Po R, Grancini G 2021 Adv. Energy Mater. 11 2100672Google Scholar

    [12]

    Subhani W S, Wang K, Du M Y, Wang X L, Liu S Z 2019 Adv. Energy Mater. 9 1803785Google Scholar

    [13]

    Guo Y X, Yin X T, Liu J, Yu Y T, Que W X 2019 Sol. RRL 3 1900135Google Scholar

    [14]

    Du J, Duan J L, Yang X Y, Duan Y Y, Zhou Q Z, Tang Q W 2021 Angew. Chem. Int. Ed. 60 10608Google Scholar

    [15]

    Wang H X, Li H Y, Cao S L, Chen J Z, Zang Z G 2020 Sol. RRL 4 2000226Google Scholar

    [16]

    Zhang W H, Xiong J, Li J H, Daoud W A 2020 Small 16 2001535Google Scholar

    [17]

    Wang G Q, Liu J Q, Lei M, Zhang W, Zhu G 2020 Electrochim. Acta 349 136354Google Scholar

    [18]

    Chen Z, Wang Q, Xu Y Y, Zhang L, Huang Y, Lyu M, Zhu J 2021 ACS Appl. Mater. Interfaces 13 24654Google Scholar

    [19]

    Wang R, Xue J J, Wang K L, Wang Z K, Luo Y, Fenning D, Huang T Y, Zhao Y P, Yang J L, Zhu J, Tan S, Houk K N, Yang Y 2019 Science 366 1509Google Scholar

    [20]

    Zhang W Y, Liu X J, He B L, Li X K, Chen H Y, Duang Y Y, Tang Q W 2020 ACS Appl. Mater. Interfaces 12 36092Google Scholar

    [21]

    Wang J P, Chen L B, Qian Z Y, Ren G Q, Wu J, Zhang H 2020 J. Mater. Chem. A 8 25336Google Scholar

    [22]

    Wang X, Ran X, Liu X, Xia Y, Chen Y, Huang W 2020 Angew. Chem. Int. Ed. 132 13456Google Scholar

    [23]

    Wang S, Ma Z R, Liu B B, Wu W C, Zhu Y, Ma R X, Wang C G 2018 Sol. RRL 2 1800034Google Scholar

    [24]

    Li X D, Zhang W X, Guo X M, Lu C Y, Wei J Y, Fang J F 2022 Science 375 434Google Scholar

    [25]

    Hu C, Bai Y, Xiao S, Ng W K, Cheung S H, So S K, Chen Q, Yang S H 2020 Sol. RRL 4 2000270Google Scholar

    [26]

    Chen W J, Li X Q, Li Y W, Li Y F 2020 Energy Environ. Sci. 13 1971Google Scholar

    [27]

    Gong J, Yang M J, Rebollar D, Rucinski J, Zhu K, Xu T 2018 Adv. Mater. 30 1800973Google Scholar

    [28]

    Wang Z, Baranwal A K, Kamarudin M K, Ng C H, Pandey M, Ma T L, Hayase S 2019 Nano Energy 59 258Google Scholar

    [29]

    Yan F R, Duan J L, Guo Q Y, Zhang Q Y, Yang P Z, Tang Q W 2023 Sci. Chin. Mater. 66 485Google Scholar

  • 图 1  (a) PTU分子结构图; (b) CsPbIBr2前驱体、PTU、PTU-CsPbIBr2前驱体混合体系的FTIR光谱图; (c) CsPbIBr2前驱体、PTU-CsPbIBr2前驱体溶液照片

    Fig. 1.  (a) Molecular structure of PTU; (b) FTIR spectra of CsPbIBr2 precursor, PTU, and PTU-CsPbIBr2 precursor; (c) photos of CsPbIBr2 and PTU-CsPbIBr2 precursor solution.

    图 2  (a) 前驱体膜在200 ℃热处理不同时间点的照片; (b) CsPbIBr2前驱体膜及在200 ℃处理10 min的XRD曲线; (c) PTU-CsPbIBr2前驱体膜及在200 ℃处理10 min和15 min的XRD曲线; (d) 不同温度热处理 PTU-CsPbIBr2前驱体膜的XRD曲线

    Fig. 2.  (a) Photos of precursor film annealed at 200 ℃ with different time; (b) XRD patterns of CsPbIBr2 precursor film annealed at 200 ℃ with different time; (c) XRD patterns of PTU-CsPbIBr2 precursor film annealed at 200 ℃ with different time; (d) XRD patterns of PTU-CsPbIBr2 precursor annealed at different temperatures.

    图 3  (a) CsPbIBr2和PTU-CsPbIBr2钙钛矿膜的SEM照片; (b) CsPbIBr2和PTU-CsPbIBr2钙钛矿膜的XRD曲线; (c) PTU的热重曲线; (d) PTU-CsPbIBr2钙钛矿膜的XPS S 2p峰; (e) CsPbIBr2和PTU-CsPbIBr2钙钛矿膜的XPS Pb 4f峰; (f) PTU-CsPbIBr2钙钛矿膜的EDX扫描照片

    Fig. 3.  (a) SEM images of CsPbIBr2 and PTU-CsPbIBr2 perovskite films; (b) XRD curves of CsPbIBr2 and PTU-CsPbIBr2 perovskite films; (c) thermogravimetry curve of PTU; (d) XPS S 2p peak of PTU-CsPbIBr2 perovskite; (e) XPS Pb 4f peak of CsPbIBr2 and PTU-CsPbIBr2 perovskite; (f) EDX mapping image of PTU-CsPbIBr2 perovskite.

    图 4  加入和未加入PTU的CsPbIBr2前驱体反应结晶形成钙钛矿过程示意图

    Fig. 4.  Schematic illustration of the crystallization process of CsPbIBr2 with and without PTU.

    图 5  (a) CsPbIBr2钙钛矿和(b) PTU-CsPbIBr2钙钛矿在湿度85%、温度30 ℃空气环境中贮存120 min的照片和XRD曲线

    Fig. 5.  Photos and XRD patterns of CsPbIBr2 (a) and PTU-CsPbIBr2 (b) perovskite stored under ambient condition with a relative humidity of 85% and a temperature of 30 ℃.

    图 6  (a) CsPbIBr2和PTU-CsPbIBr2钙钛矿膜的紫外-可见吸收光谱和稳态PL光谱; (b) CsPbIBr2和PTU-CsPbIBr2钙钛矿组成的单电子器件(插图)的空间电荷限制电流图

    Fig. 6.  (a) UV-vis absorption spectra and steady-state PL of CsPbIBr2 and PTU-CsPbIBr2 perovskite films; (b) SCLC curves based on the electron-only device (the inset) with CsPbIBr2 and PTU-CsPbIBr2 perovskite.

    图 7  (a)碳基钙钛矿太阳能电池的光电流密度-电压曲线; (b) CsPbIBr2前驱体中加入不同量PTU所组装的钙钛矿太阳能电池的光电性能曲线; (c)未密封PTU-CsPbIBr2钙钛矿电池在空气环境中效率随时间的变化

    Fig. 7.  (a) Current density-voltage curves of carbon-based PSCs with CsPbIBr2 and PTU-CsPbIBr2 perovskite; (b) current density-voltage curves of PSCs based on PTU-CsPbIBr2 with different amounts of PTU; (c) PCE variation of unencapsulated device stored in ambient condition.

  • [1]

    Jia X, Zou C T, Tao S X, Sun K. Zhao Y X, Yang S F, Chen M, Wang M K, Yuan Y B, Gao F, Wei Z H, Zhang L J, Yip H, Liu M Z, Shen Q, Yin L W, Tan H R, Jin Z W, Ding L M 2019 Sci. Bull. 64 1532Google Scholar

    [2]

    Tai Q, Tang K C, Yan F 2019 Energy Environ. Sci. 12 2375Google Scholar

    [3]

    Li B, Fu L, Li S, Chang B H, Li H, Yin L W 2019 J. Mater. Chem. A 7 20494Google Scholar

    [4]

    Faheem M B, Khan B, Feng C, Raziq F, Li Y B, Yao Y Q 2020 ACS Energy Lett. 5 290Google Scholar

    [5]

    Xiang W C, Tress W 2019 Adv. Mater. 31 1902851Google Scholar

    [6]

    Du Y C, Tian Q W, Chang X M, Fan J J, He X L, Ren X D, Zhao K, Liu S Z 2022 Adv. Mater. 34 2106750Google Scholar

    [7]

    Yu B C, Shi J J, Tan S, Zhao W Y, Hu H J, Luo Y H, Li D M, Meng Q B 2021 Angew. Chem. Int. Ed. 60 13436Google Scholar

    [8]

    Yoon S M, Min H, Kim J B, Lee S K, Seok S I 2021 Joule 5 183Google Scholar

    [9]

    Duan J L, Zhao Y Y, Yang X Y, Wang Y D, He B L, Tang Q W 2018 Adv. Energy Mater. 8 1802386Google Scholar

    [10]

    马书鹏, 林飞宇, 罗媛, 朱刘, 郭学益, 杨英 2022 物理学报 71 158101Google Scholar

    Ma S P, Lin F Y, Luo Y, Zhu L, Guo X Y, Yang Y 2022 Acta Phys. Sin. 71 158101Google Scholar

    [11]

    Montecucco R, Quadrivi E, Po R, Grancini G 2021 Adv. Energy Mater. 11 2100672Google Scholar

    [12]

    Subhani W S, Wang K, Du M Y, Wang X L, Liu S Z 2019 Adv. Energy Mater. 9 1803785Google Scholar

    [13]

    Guo Y X, Yin X T, Liu J, Yu Y T, Que W X 2019 Sol. RRL 3 1900135Google Scholar

    [14]

    Du J, Duan J L, Yang X Y, Duan Y Y, Zhou Q Z, Tang Q W 2021 Angew. Chem. Int. Ed. 60 10608Google Scholar

    [15]

    Wang H X, Li H Y, Cao S L, Chen J Z, Zang Z G 2020 Sol. RRL 4 2000226Google Scholar

    [16]

    Zhang W H, Xiong J, Li J H, Daoud W A 2020 Small 16 2001535Google Scholar

    [17]

    Wang G Q, Liu J Q, Lei M, Zhang W, Zhu G 2020 Electrochim. Acta 349 136354Google Scholar

    [18]

    Chen Z, Wang Q, Xu Y Y, Zhang L, Huang Y, Lyu M, Zhu J 2021 ACS Appl. Mater. Interfaces 13 24654Google Scholar

    [19]

    Wang R, Xue J J, Wang K L, Wang Z K, Luo Y, Fenning D, Huang T Y, Zhao Y P, Yang J L, Zhu J, Tan S, Houk K N, Yang Y 2019 Science 366 1509Google Scholar

    [20]

    Zhang W Y, Liu X J, He B L, Li X K, Chen H Y, Duang Y Y, Tang Q W 2020 ACS Appl. Mater. Interfaces 12 36092Google Scholar

    [21]

    Wang J P, Chen L B, Qian Z Y, Ren G Q, Wu J, Zhang H 2020 J. Mater. Chem. A 8 25336Google Scholar

    [22]

    Wang X, Ran X, Liu X, Xia Y, Chen Y, Huang W 2020 Angew. Chem. Int. Ed. 132 13456Google Scholar

    [23]

    Wang S, Ma Z R, Liu B B, Wu W C, Zhu Y, Ma R X, Wang C G 2018 Sol. RRL 2 1800034Google Scholar

    [24]

    Li X D, Zhang W X, Guo X M, Lu C Y, Wei J Y, Fang J F 2022 Science 375 434Google Scholar

    [25]

    Hu C, Bai Y, Xiao S, Ng W K, Cheung S H, So S K, Chen Q, Yang S H 2020 Sol. RRL 4 2000270Google Scholar

    [26]

    Chen W J, Li X Q, Li Y W, Li Y F 2020 Energy Environ. Sci. 13 1971Google Scholar

    [27]

    Gong J, Yang M J, Rebollar D, Rucinski J, Zhu K, Xu T 2018 Adv. Mater. 30 1800973Google Scholar

    [28]

    Wang Z, Baranwal A K, Kamarudin M K, Ng C H, Pandey M, Ma T L, Hayase S 2019 Nano Energy 59 258Google Scholar

    [29]

    Yan F R, Duan J L, Guo Q Y, Zhang Q Y, Yang P Z, Tang Q W 2023 Sci. Chin. Mater. 66 485Google Scholar

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  • 被引次数: 0
出版历程
  • 收稿日期:  2023-04-13
  • 修回日期:  2023-05-14
  • 上网日期:  2023-06-02
  • 刊出日期:  2023-08-05

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