Two-dimensional halide perovskite lateral epitaxial heterostructures

卤化物 钙钛矿(结构) 异质结 外延 半导体 材料科学 光电子学 化学 纳米技术 结晶学 无机化学 图层(电子)
作者
Enzheng Shi,Biao Yuan,Stephen B. Shiring,Yao Gao,Akriti Akriti,Yunfan Guo,Cong Su,Minliang Lai,Peidong Yang,Jing Kong,Brett M. Savoie,Yi Yu,Letian Dou
出处
期刊:Nature [Nature Portfolio]
卷期号:580 (7805): 614-620 被引量:360
标识
DOI:10.1038/s41586-020-2219-7
摘要

Epitaxial heterostructures based on oxide perovskites and III–V, II–VI and transition metal dichalcogenide semiconductors form the foundation of modern electronics and optoelectronics1–7. 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 lasers8–15. Their inherently soft crystal lattice allows greater tolerance to lattice mismatch, making them promising for heterostructure formation and semiconductor integration16,17. 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 widths18–21, 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 importance22–26. 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. An epitaxial growth strategy that improves the stability of two-dimensional halide perovskites by inhibiting ion diffusion in their heterostructures using rigid π-conjugated ligands is demonstrated, and shows near-atomically sharp interfaces.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
llg发布了新的文献求助10
1秒前
小白发布了新的文献求助10
1秒前
bc应助安详的惜梦采纳,获得10
1秒前
3秒前
风中小懒虫完成签到,获得积分10
3秒前
舒心的泥猴桃完成签到,获得积分10
8秒前
bc应助小白采纳,获得10
14秒前
bc应助小白采纳,获得10
14秒前
科研通AI5应助小白采纳,获得30
14秒前
灰灰喵完成签到 ,获得积分10
16秒前
19秒前
小马甲应助赵文若采纳,获得10
21秒前
hs发布了新的文献求助10
26秒前
打打应助科研通管家采纳,获得10
27秒前
科研通AI2S应助科研通管家采纳,获得10
27秒前
Hello应助科研通管家采纳,获得10
27秒前
冰魂应助科研通管家采纳,获得10
27秒前
共享精神应助科研通管家采纳,获得10
27秒前
充电宝应助科研通管家采纳,获得10
28秒前
在水一方应助科研通管家采纳,获得10
28秒前
华仔应助科研通管家采纳,获得10
28秒前
wanci应助科研通管家采纳,获得10
28秒前
传奇3应助科研通管家采纳,获得30
28秒前
NexusExplorer应助科研通管家采纳,获得10
28秒前
NexusExplorer应助科研通管家采纳,获得10
28秒前
28秒前
30秒前
31秒前
科研通AI5应助wankai采纳,获得10
32秒前
JlkD完成签到,获得积分10
33秒前
35秒前
yannnis发布了新的文献求助10
36秒前
赵文若发布了新的文献求助10
36秒前
hs完成签到,获得积分10
37秒前
40秒前
41秒前
41秒前
41秒前
42秒前
42秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
Continuum Thermodynamics and Material Modelling 2000
Encyclopedia of Geology (2nd Edition) 2000
105th Edition CRC Handbook of Chemistry and Physics 1600
Maneuvering of a Damaged Navy Combatant 650
Периодизация спортивной тренировки. Общая теория и её практическое применение 310
Mixing the elements of mass customisation 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3778812
求助须知:如何正确求助?哪些是违规求助? 3324352
关于积分的说明 10218073
捐赠科研通 3039436
什么是DOI,文献DOI怎么找? 1668089
邀请新用户注册赠送积分活动 798545
科研通“疑难数据库(出版商)”最低求助积分说明 758437