GSTDTAP  > 地球科学
DOI10.1038/s41586-020-2219-7
Two-dimensional halide perovskite lateral epitaxial heterostructures
Cabrita, Rita; Lauss, Martin; Sanna, Adriana; Donia, Marco; Larsen, Mathilde; Mitra, Shamik; Johansson, Iva; Phung, Bengt; Harbst, Katja; Vallon-Christersson, Johan; van Schoiack, Alison; Lovgren, Kristina; Warren, Sarah; Jirstrom, Karin; Olsson, Hakan; Pietras, Kristian; Ingvar, Christian; Isaksson, Karolin
2020-03-20
发表期刊NATURE
ISSN0028-0836
EISSN1476-4687
出版年2020
卷号580期号:7805页码:614-+
文章类型Article
语种英语
国家USA; Peoples R China
英文关键词

Epitaxial heterostructures based on oxide perovskites and III-V, II-VI and transition metal dichalcogenide semiconductors form the foundation of modern electronics and optoelectronics(1-7). 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(8-15). Their inherently soft crystal lattice allows greater tolerance to lattice mismatch, making them promising for heterostructure formation and semiconductor integration(16,17). 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(18-21), 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(22-26). Here we report an effective strategy to substantially inhibit in-plane ion diffusion in two-dimensional halide perovskites by incorporating rigid pi-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.


An epitaxial growth strategy that improves the stability of two-dimensional halide perovskites by inhibiting ion diffusion in their heterostructures using rigid pi-conjugated ligands is demonstrated, and shows near-atomically sharp interfaces.


领域地球科学 ; 气候变化 ; 资源环境
收录类别SCI-E
WOS记录号WOS:000529600500011
WOS关键词BASIS-SETS ; NANOCRYSTALS ; TRANSITION ; GROWTH
WOS类目Multidisciplinary Sciences
WOS研究方向Science & Technology - Other Topics
引用统计
文献类型期刊论文
条目标识符http://119.78.100.173/C666/handle/2XK7JSWQ/281534
专题地球科学
资源环境科学
气候变化
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GB/T 7714
Cabrita, Rita,Lauss, Martin,Sanna, Adriana,et al. Two-dimensional halide perovskite lateral epitaxial heterostructures[J]. NATURE,2020,580(7805):614-+.
APA Cabrita, Rita.,Lauss, Martin.,Sanna, Adriana.,Donia, Marco.,Larsen, Mathilde.,...&Isaksson, Karolin.(2020).Two-dimensional halide perovskite lateral epitaxial heterostructures.NATURE,580(7805),614-+.
MLA Cabrita, Rita,et al."Two-dimensional halide perovskite lateral epitaxial heterostructures".NATURE 580.7805(2020):614-+.
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