材料科学
半导体
纳米技术
金属
多态性(计算机科学)
化学物理
相(物质)
相变
化学气相沉积
光电子学
结晶学
凝聚态物理
化学
物理
基因型
有机化学
冶金
基因
生物化学
作者
Ji Ho Sung,Heeok Heo,Saerom Si,Yong Hyeon Kim,Hyeong Rae Noh,Kyung Song,Juho Kim,Chang‐Soo Lee,Seung‐Young Seo,Dong‐Hwi Kim,Hyoung Kug Kim,Han Woong Yeom,Tae‐Hwan Kim,Si‐Young Choi,Jun Sung Kim,Moon‐Ho Jo
标识
DOI:10.1038/nnano.2017.161
摘要
Crystal polymorphism selectively stabilizes the electronic phase of atomically thin transition-metal dichalcogenides (TMDCs) as metallic or semiconducting, suggesting the potential to integrate these polymorphs as circuit components in two-dimensional electronic circuitry. Developing a selective and sequential growth strategy for such two-dimensional polymorphs in the vapour phase is a critical step in this endeavour. Here, we report on the polymorphic integration of distinct metallic (1T′) and semiconducting (2H) MoTe2 crystals within the same atomic planes by heteroepitaxy. The realized polymorphic coplanar contact is atomically coherent, and its barrier potential is spatially tight-confined over a length of only a few nanometres, with a lowest contact barrier height of ∼25 meV. We also demonstrate the generality of our synthetic integration approach for other TMDC polymorph films with large areas. Sequential heteroepitaxy of transition-metal dichalcogenide polymorphs with different electronic properties is used to build coplanar ultrathin circuitry with atomic-scale precision.
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