材料科学
简并能级
凝聚态物理
光电子学
图层(电子)
工作(物理)
纳米技术
领域(数学)
密度泛函理论
结晶学
作者
Seoungbum Lim,Xingguo Wang,Chan How Oh,Yuhui Yang,Yue Gong,Chenyu Zang,Manlin Luo,Xingli Wang,Philippe Coquet,Edwin Hang Tong Teo,Sang Hoon Chae,Beng Kang Tay
标识
DOI:10.1021/acsami.5c25656
摘要
Tin diselenide (SnSe 2 ) is a two-dimensional (2D) semiconductor with a high electron affinity (∼5.2 eV) and inherent n + -type conductivity. While conventional chemical vapor deposition (CVD) has been investigated for the growth of SnSe 2, the domain sizes are typically limited to ∼50 μm. This limitation arises primarily from difficulties in precise control of the thermodynamics of nucleation and growth along with the kinetics of vapor-phase transport. To address this issue, we employed flux-assisted growth (FAG) to facilitate liquid-phase precursor transport via a molten flux. As a result, we achieved crystalline SnSe 2 flakes with significantly enlarged domain sizes exceeding 300 μm. The synthesized SnSe 2 exhibits a well-ordered 1T-phase lattice structure, a high Hall mobility of 262.5 cm 2 ·V –1 ·s –1, and an electron concentration of 8.23 × 10 13 cm –2, confirming its degenerate n-type nature. Furthermore, the SnSe 2 -based devices show reproducible photoresponse cycles governed by trap-mediated processes yielding a multitime scale fading memory. Our findings provide insights into the feasibility of flux-grown SnSe 2 for p–n + van der Waals tunneling heterostructures and in-sensor reservoir computing.
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