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二维卤化物钙钛矿横向外延异质结构。

Two-dimensional halide perovskite lateral epitaxial heterostructures.

机构信息

Davidson School of Chemical Engineering, Purdue University, West Lafayette, IN, USA.

School of Physical Science and Technology, ShanghaiTech University, Shanghai, China.

出版信息

Nature. 2020 Apr;580(7805):614-620. doi: 10.1038/s41586-020-2219-7. Epub 2020 Apr 29.

Abstract

Epitaxial heterostructures based on oxide perovskites and III-V, II-VI and transition metal dichalcogenide semiconductors form the foundation of modern electronics and optoelectronics. Halide perovskites-an emerging family of tunable semiconductors with desirable properties-are attractive for applications such as solution-processed solar cells, light-emitting diodes, detectors and lasers. Their inherently soft crystal lattice allows greater tolerance to lattice mismatch, making them promising for heterostructure formation and semiconductor integration. Atomically sharp epitaxial interfaces are necessary to improve performance and for device miniaturization. However, epitaxial growth of atomically sharp heterostructures of halide perovskites has not yet been achieved, owing to their high intrinsic ion mobility, which leads to interdiffusion and large junction widths, and owing to their poor chemical stability, which leads to decomposition of prior layers during the fabrication of subsequent layers. Therefore, understanding the origins of this instability and identifying effective approaches to suppress ion diffusion are of great importance. Here we report an effective strategy to substantially inhibit in-plane ion diffusion in two-dimensional halide perovskites by incorporating rigid π-conjugated organic ligands. We demonstrate highly stable and tunable lateral epitaxial heterostructures, multiheterostructures and superlattices. Near-atomically sharp interfaces and epitaxial growth are revealed by low-dose aberration-corrected high-resolution transmission electron microscopy. Molecular dynamics simulations confirm the reduced heterostructure disorder and larger vacancy formation energies of the two-dimensional perovskites in the presence of conjugated ligands. These findings provide insights into the immobilization and stabilization of halide perovskite semiconductors and demonstrate a materials platform for complex and molecularly thin superlattices, devices and integrated circuits.

摘要

基于氧化物钙钛矿以及 III-V、II-VI 和过渡金属二卤化物半导体的外延异质结构是现代电子学和光电学的基础。卤化物钙钛矿——一种具有理想性质的新兴可调半导体家族——在溶液处理的太阳能电池、发光二极管、探测器和激光器等应用中具有吸引力。它们固有的软晶格允许更大的晶格失配容忍度,使它们成为异质结构形成和半导体集成的有前途的材料。原子级陡峭的外延界面对于提高性能和器件小型化是必要的。然而,由于卤化物钙钛矿具有较高的本征离子迁移率,导致互扩散和较大的结宽,以及较差的化学稳定性,导致在随后的层制造过程中先前层的分解,因此尚未实现原子级陡峭的卤化物钙钛矿外延异质结构的生长。因此,了解这种不稳定性的起源并确定有效抑制离子扩散的方法非常重要。在这里,我们报告了一种通过引入刚性π共轭有机配体来有效抑制二维卤化物钙钛矿面内离子扩散的策略。我们展示了高度稳定和可调谐的横向外延异质结构、多异质结构和超晶格。低剂量像差校正高分辨率透射电子显微镜揭示了近乎原子级陡峭的界面和外延生长。分子动力学模拟证实了二维钙钛矿在共轭配体存在下的异质结构无序程度降低和空位形成能增大。这些发现为卤化物钙钛矿半导体的固定和稳定提供了深入的了解,并展示了用于复杂和分子薄超晶格、器件和集成电路的材料平台。

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