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Mixed Cation FA(x)PEA(1-x)PbI(3) with Enhanced Phase and Ambient Stability toward High-Performance Perovskite Solar Cells

机译:对高性能钙钛矿太阳能电池具有增强的相和环境稳定性的混合阳离子FA(x)PEA(1-x)PbI(3)

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摘要

In this work, different from the commonly explored strategy of incorporating a smaller cation, MA(+) and Cs+ into FAPbI(3) lattice to improve efficiency and stability, it is revealed that the introduction of phenylethylammonium iodide (PEAI) into FAPbI(3) perovksite to form mixed cation FA(x)PEA(1-x)PbI(3) can effectively enhance both phase and ambient stability of FAPbI(3) as well as the resulting performance of the derived devices. From our experimental and theoretical calculation results, it is proposed that the larger PEA cation is capable of assembling on both the lattice surface and grain boundaries to form quais-3D perovskite structures. The surrounding of PEA(+) ions at the crystal grain boundaries not only can serve as molecular locks to tighten FAPbI(3) domains but also passivate the surface defects to improve both phase and moisture stablity. Consequently, a high-performance (PCE: 17.7%) and ambient stable FAPbI(3) solar cell could be developed.
机译:在这项工作中,与通常探索的将较小的阳离子,MA(+)和Cs +掺入FAPbI(3)晶格以提高效率和稳定性的策略不同,它揭示了将苯基乙基碘化铵(PEAI)引入FAPbI(3) Perovksite形成混合阳离子FA(x)PEA(1-x)PbI(3)可以有效地增强FAPbI(3)的相和环境稳定性以及衍生设备的性能。从我们的实验和理论计算结果来看,建议较大的PEA阳离子能够在晶格表面和晶界上组装形成准3D钙钛矿结构。在晶粒边界处的PEA(+)离子周围不仅可以充当分子锁来拧紧FAPbI(3)域,而且可以钝化表面缺陷以改善相和水分稳定性。因此,可以开发出高性能(PCE:17.7%)和环境稳定的FAPbI(3)太阳能电池。

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  • 来源
    《Advanced energy materials》 |2017年第1期|1601307.1-1601307.9|共9页
  • 作者单位

    Univ Washington, Dept Mat Sci & Engn, Seattle, WA 98195 USA;

    Univ Washington, Dept Mat Sci & Engn, Seattle, WA 98195 USA;

    Univ Washington, Dept Mat Sci & Engn, Seattle, WA 98195 USA;

    Univ Washington, Dept Chem, Seattle, WA 98195 USA;

    Univ Washington, Dept Chem, Seattle, WA 98195 USA;

    Univ Washington, Dept Chem, Seattle, WA 98195 USA;

    Univ Washington, Dept Chem, Seattle, WA 98195 USA;

    Tsinghua Univ, Dept Chem, Minist Educ, Key Lab Organ Optoelect & Mol Engn, Beijing 100084, Peoples R China;

    Univ Washington, Dept Mat Sci & Engn, Seattle, WA 98195 USA|Univ Washington, Dept Chem, Seattle, WA 98195 USA;

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