纳米片
材料科学
光探测
锌
成核
外延
紫外线
图层(电子)
离子键合
化学工程
纳米技术
光电子学
光电探测器
化学
离子
有机化学
冶金
工程类
作者
Ryunosuke Matsumura,Yuta Kazama,Hikaru Saito,Takao Yasui,Yasutaka Matsuo,Akira Nasu,Hiroaki Kobayashi,Sayuki Oka,Narathon Khemasiri,Yohei Yomogida,Kazuki Nagashima
标识
DOI:10.1021/acsanm.4c07224
摘要
Zinc oxide (ZnO) nanosheets have shown great promise for ultraviolet (UV) photodetectors due to their excellent optoelectronic properties and atomically thin structure. Surfactant-assisted ionic layer epitaxy (ILE) is a simple and scalable technique for synthesizing monolayered ZnO nanosheets; however, the formation of a byproduct is inevitable and detrimental for optoelectronic device applications. This study demonstrates a rational strategy for the selective growth of ZnO nanosheets in ILE growth without byproduct formation. The detailed investigation revealed that the formation of byproducts originates from surfactant-induced heterogeneous nucleation. We found that increasing the surfactant concentration suppresses the byproduct formation by localizing the zinc precursor at the water–air interface and opens a concentration window for promoting nanosheet growth. By precise control of the zinc precursor concentration within the concentration window, a selective growth of ca. 1-nm-thick ZnO nanosheets was successfully achieved. A device composed of a single ZnO nanosheet demonstrated a fast-response UV photodetection (rise time/recovery time = 12.3 ms/24.7 ms), which is shorter than the previously reported ZnO nanosheet devices.
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