基于 CdSe 量子点/In-Ga-Zn-O 混合通道的可见光刺激突触光电晶体管

IF 4.703 3区 材料科学 Nanoscale Research Letters Pub Date : 2022-10-27 DOI:10.1186/s11671-022-03739-8
En-bo Fu, Yu Liu, Xiang-Rui Hou, Ye Feng, Chun-lei Yang, Yan Shao
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引用次数: 0

摘要

光刺激突触设备具有独特的性能,包括宽带宽、低功耗和卓越的并行性,因此是开发人工智能系统的理想候选设备。开发这类设备的关键是在其中实现光电突触行为。本研究提出了基于硒化镉量子点(CdSe QD)/非晶 In-Ga-Zn-O 混合通道的可见光刺激突触晶体管。这种设计不仅能提高光生载流子的电荷分离效率,还能引起光电流的延迟衰减。电荷分离效率的提高显著增强了光电特性,而光电流的延迟衰减则促成了光电突触行为的实现。这种简单高效的光刺激光电晶体管制造方法可能会为人工智能系统的开发带来新的研究进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Visible-Light-Stimulated Synaptic Phototransistors Based on CdSe Quantum Dot/In–Ga–Zn–O Hybrid Channels

Light-stimulated synaptic devices are promising candidates for the development of artificial intelligence systems because of their unique properties, which include broad bandwidths, low power consumption, and superior parallelism. The key to develop such devices is the realization of photoelectric synaptic behavior in them. In this work, visible-light-stimulated synaptic transistors based on CdSe quantum dot (CdSe QD)/amorphous In–Ga–Zn–O hybrid channels are proposed. This design can not only improve the charge separation efficiency of the photogenerated carriers, but also can induce delayed decay of the photocurrent. The improved charge separation efficiency enhances the photoelectric properties significantly, while the delayed decay of the photocurrent led to the realization of photoelectric synaptic behaviors. This simple and efficient method of fabricating light-stimulated phototransistors may inspire new research progress into the development of artificial intelligence systems.

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来源期刊
Nanoscale Research Letters
Nanoscale Research Letters NANOSCIENCE & NANOTECHNOLOGY-MATERIALS SCIENCE, MULTIDISCIPLINARY
CiteScore
15.00
自引率
0.00%
发文量
110
审稿时长
2.5 months
期刊介绍: Nanoscale Research Letters (NRL) provides an interdisciplinary forum for communication of scientific and technological advances in the creation and use of objects at the nanometer scale. NRL is the first nanotechnology journal from a major publisher to be published with Open Access.
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