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首页> 外文期刊>Energy & environmental science >An in situ cross-linked 1D/3D perovskite heterostructure improves the stability of hybrid perovskite solar cells for over 3000 h operation
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An in situ cross-linked 1D/3D perovskite heterostructure improves the stability of hybrid perovskite solar cells for over 3000 h operation

机译:原位交联的1D / 3D钙钛矿异质结构可提高杂交钙钛矿太阳能电池的稳定性超过3000小时

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摘要

Long-term stability is an essential requirement for perovskite solar cells (PSCs) to be commercially viable. Heterojunctions built by low-dimensional and three-dimensional perovskites (1D/3D or 2D/3D) help to improve the stability of PSCs. However, the insulated organic cations of low-dimensional perovskite impede the transport of carriers, decreasing the power conversion efficiency (PCE) of PSCs. Herein, we introduce an in situ cross-linking polymerizable propargylammonium (PA(+)) to the 3D perovskite film at surfaces and grain boundaries to form a 1D/3D perovskite heterostructure. This passivation strategy not only significantly improves the interfacial carrier transport but also releases residual tensile strain in perovskite films. As a result, the corresponding devices achieve a champion PCE of 21.19%, while maintaining 93% of their initial efficiency after 3055 h of continuous illumination under maximum power point (MPP) operating conditions.
机译:长期稳定性是钙钛矿太阳能电池(PSC)在商业上可行的必要要求。由低维和三维Perovskites(1D / 3D或2D / 3D)构建的异电功能有助于提高PSC的稳定性。然而,低维Perovskite的绝缘有机阳离子阻碍了载体的运输,降低了PSC的功率转换效率(PCE)。在此,我们将原位交联可聚合炔丙基铵(PA(+))在表面和晶界处的3D钙钛矿膜中引入3D钙钛矿膜以形成1D / 3D钙钛矿异质结构。这种钝化策略不仅显着改善了界面载体运输,而且还显着改善了钙钛矿薄膜中的残留拉伸菌株。结果,相应的装置实现了21.19%的冠军PCE,同时在最大功率点(MPP)操作条件下连续照明3055小时后保持93%的初始效率。

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  • 来源
    《Energy & environmental science 》 |2020年第11期| 4344-4352| 共9页
  • 作者单位

    Beijing Inst Technol BIT Beijing Key Lab Nanophoton & Ultrafine Optoelect Expt Ctr Adv Mat Sch Mat Sci & Engn Beijing 100081 Peoples R China;

    Beijing Inst Technol BIT Beijing Key Lab Nanophoton & Ultrafine Optoelect Expt Ctr Adv Mat Sch Mat Sci & Engn Beijing 100081 Peoples R China;

    Peking Univ Coll Engn Dept Mat Sci & Engn Beijing 100871 Peoples R China;

    Peking Univ Coll Engn Dept Mat Sci & Engn Beijing 100871 Peoples R China;

    Beijing Inst Technol BIT Beijing Key Lab Nanophoton & Ultrafine Optoelect Expt Ctr Adv Mat Sch Mat Sci & Engn Beijing 100081 Peoples R China;

    Beijing Inst Technol BIT Beijing Key Lab Nanophoton & Ultrafine Optoelect Expt Ctr Adv Mat Sch Mat Sci & Engn Beijing 100081 Peoples R China;

    Beijing Inst Technol BIT Beijing Key Lab Nanophoton & Ultrafine Optoelect Expt Ctr Adv Mat Sch Mat Sci & Engn Beijing 100081 Peoples R China;

    Beijing Inst Technol BIT Beijing Key Lab Nanophoton & Ultrafine Optoelect Expt Ctr Adv Mat Sch Mat Sci & Engn Beijing 100081 Peoples R China;

    BIT Sch Aerosp Engn Beijing 100081 Peoples R China;

    BIT Sch Aerosp Engn Beijing 100081 Peoples R China;

    BIT Sch Aerosp Engn Beijing 100081 Peoples R China;

    Beijing Inst Technol BIT Beijing Key Lab Nanophoton & Ultrafine Optoelect Expt Ctr Adv Mat Sch Mat Sci & Engn Beijing 100081 Peoples R China;

    Peking Univ Coll Engn Dept Mat Sci & Engn Beijing 100871 Peoples R China;

    Beijing Inst Technol BIT Beijing Key Lab Nanophoton & Ultrafine Optoelect Expt Ctr Adv Mat Sch Mat Sci & Engn Beijing 100081 Peoples R China|Beijing Inst Technol BIT Adv Res Inst Multidisciplinary Sci Beijing 100081 Peoples R China;

    Beijing Inst Technol BIT Beijing Key Lab Nanophoton & Ultrafine Optoelect Expt Ctr Adv Mat Sch Mat Sci & Engn Beijing 100081 Peoples R China|Beijing Inst Technol Chongqing Innovat Ctr Chongqing 401120 Peoples R China;

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