Journal
NANO LETTERS
Volume 23, Issue 3, Pages 1077-1084Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.2c04785
Keywords
scanning tunneling spectroscopy; indium selenide; order-disorder transition; layer-by-layer growth
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Understanding the polymorph transition and crystal-amorphous phase transition is crucial for exploring the potential of In2Se3 in resistive memory storage. By monitoring the growth of beta-In(2)Se(3 )layer by layer during molecular beam epitaxy (MBE), we observed a cyclic order-disorder transition where the material exhibited a glassy-like metastable subunit cell film with n < 5 sublayers and highly crystalline beta-In2Se3 at n = 5 layers. The alternating behavior between the indium-cluster layer and In-Se solid solution suggests the diffusion, aggregation, and intermixing of In and Se atoms. These dynamic properties contribute to a defect-driven memory resistive behavior different from the ferroelectric switching of alpha-In2Se3.
It is important to understand the polymorph transition and crystal-amorphous phase transition in In2Se3 to tap the potential of this material for resistive memory storage. By monitoring layer-by-layer growth of beta-In(2)Se(3 )during molecular beam epitaxy (MBE), we are able to identify a cyclical order- disorder transition characterized by a periodic alternation between a glassy-like metastable subunit cell film consisting of n < 5 sublayers (nth layers = the number of subunit cell layers), and a highly crystalline beta-In2Se3 at n = 5 layers. The glassy phase shows an odd-even alternation between the indium-cluster layer (n = 1, 3) and an In-Se solid solution (n = 2, 4), which suggests the ability of In and Se atoms to diffuse, aggregate, and intermix. These dynamic natures of In and Se atoms contribute to a defect-driven memory resistive behavior in current-voltage sweeps that is different from the ferroelectric switching of alpha-In2Se3 .
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