Lattice-Matched Heterogeneous Nucleation Eliminates Defective Buried Interfaces in Halide Perovskites

被引:2
作者
Ahlawat, Paramvir [1 ]
Clementi, Cecilia [2 ,3 ]
Musil, Felix [2 ]
Filip, Maria-Andreea [1 ]
Dar, M. Ibrahim [4 ]
机构
[1] Univ Cambridge, Yusuf Hamied Dept Chem, Cambridge CB2 1EW, England
[2] Free Univ Berlin, Dept Phys, D-14195 Berlin, Germany
[3] Rice Univ, Ctr Theoret Biol Phys, Houston, TX 77005 USA
[4] Univ Cambridge, Dept Phys, Cavendish Lab, Cambridge CB3 0HE, England
基金
英国工程与自然科学研究理事会; 瑞士国家科学基金会;
关键词
MOLECULAR-DYNAMICS; CRYSTAL-GROWTH; QUANTUM DOTS; PHASE SEGREGATION; SOLAR-CELLS; FORCE-FIELD; NANOCRYSTALS; CSPBBR3; SUPERCONDUCTIVITY; FILMS;
D O I
10.1021/acs.chemmater.4c03034
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Advancements in the formation of metal halide perovskite semiconductors have led to solar cells and light-emitting devices with efficiencies exceeding 25%. To push these performances beyond theoretical limits and achieve long-term stability, a fundamental understanding of the structural evolution at the interface between perovskites and charge-transporting materials is essential. In this study, we perform molecular dynamics simulations to investigate the atomic-scale processes involved in the nucleation and growth of cesium lead bromide perovskite on commonly used oxide interfaces. Our results reveal that the perovskite crystallizes through a heteroepitaxial mechanism, which can induce the formation of dislocations, voids, and defects at the buried interface as well as grain boundaries within the bulk crystal. From simulations, we find that the lattice-matched interfaces promote epitaxially ordered growth of the perovskite, potentially mitigating defect formation at the interface. Eliminating these defects could arguably pave the way for achieving the long-term stability required for high-efficiency perovskite solar cells and light-emitting diodes.
引用
收藏
页码:2177 / 2191
页数:15
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