Singh Ajeet, Yuan Biao, Rahman Md Habibur, Yang Hanjun, De Angana, Park Jee Yung, Zhang Shuchen, Huang Libai, Mannodi-Kanakkithodi Arun, Pennycook Timothy J, Dou Letian
Davidson School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.
Department of Chemistry, Indian Institute of Technology Delhi, New Delhi 110016, India.
J Am Chem Soc. 2023 Sep 13;145(36):19885-19893. doi: 10.1021/jacs.3c06127. Epub 2023 Aug 31.
Epitaxial heterostructures of two-dimensional (2D) halide perovskites offer a new platform for studying intriguing structural, optical, and electronic properties. However, difficulties with the stability of Pb- and Sn-based heterostructures have repeatedly slowed the progress. Recently, Pb-free halide double perovskites are gaining a lot of attention due to their superior stability and greater chemical diversity, but they have not been successfully incorporated into epitaxial heterostructures for further investigation. Here, we report epitaxial core-shell heterostructures via growing Pb-free double perovskites (involving combinations of Ag(I)-Bi(III), Ag-Sb, Ag-In, Na-Bi, Na-Sb, and Na-In) around Pb perovskite 2D crystals. Distinct from Pb-Pb and Pb-Sn perovskite heterostructures, growths of the Pb-free shell at 45° on the (100) surface of the lead perovskite core are observed in all Pb-free cases. The in-depth structural analysis carried out with electron diffraction unequivocally demonstrates the growth of the Pb-free shell along the [110] direction of the Pb perovskite, which is likely due to the relatively lower surface energy of the (110) surface. Furthermore, an investigation of anionic interdiffusion across heterostructure interfaces under the influence of heat was carried out. Interestingly, halide anion diffusion in the Pb-free 2D perovskites is found to be significantly suppressed as compared to Pb-based 2D perovskites. The great structural tunability and excellent stability of Pb-free perovskite heterostructures may find uses in electronic and optoelectronic devices in the near future.
二维(2D)卤化物钙钛矿的外延异质结构为研究有趣的结构、光学和电子特性提供了一个新平台。然而,基于铅和锡的异质结构的稳定性问题反复阻碍了研究进展。最近,无铅卤化物双钙钛矿因其卓越的稳定性和更丰富的化学多样性而备受关注,但尚未成功纳入外延异质结构进行进一步研究。在此,我们报告了通过在铅钙钛矿二维晶体周围生长无铅双钙钛矿(涉及Ag(I)-Bi(III)、Ag-Sb、Ag-In、Na-Bi、Na-Sb和Na-In的组合)形成的外延核壳异质结构。与铅-铅和铅-锡钙钛矿异质结构不同,在所有无铅情况下,均观察到无铅壳在铅钙钛矿核的(100)表面以45°角生长。利用电子衍射进行的深入结构分析明确表明,无铅壳沿铅钙钛矿的[110]方向生长,这可能是由于(110)表面的表面能相对较低。此外,还研究了在热影响下异质结构界面处的阴离子相互扩散。有趣的是,与基于铅的二维钙钛矿相比,发现无铅二维钙钛矿中的卤化物阴离子扩散受到显著抑制。无铅钙钛矿异质结构的巨大结构可调性和出色稳定性可能在不久的将来用于电子和光电器件。