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介观氧化石墨烯器件中负微分电阻的观测

Observation of negative differential resistance in mesoscopic graphene oxide devices.

作者信息

Rathi Servin, Lee Inyeal, Kang Moonshik, Lim Dongsuk, Lee Yoontae, Yamacli Serhan, Joh Han-Ik, Kim Seongsu, Kim Sang-Woo, Yun Sun Jin, Choi Sukwon, Kim Gil-Ho

机构信息

Samsung-SKKU Graphene Center, Sungkyunkwan Advanced Institute of Nanotechnology (SAINT) and School of Electronics and Electrical Engineering, Sungkyunkwan University, Suwon, 16419, Korea.

Manufacturing Engineering Team, Memory Division, Samsung Electronics Co, Hwasung, 18396, Korea.

出版信息

Sci Rep. 2018 May 8;8(1):7144. doi: 10.1038/s41598-018-22355-0.

Abstract

The fractions of various functional groups in graphene oxide (GO) are directly related to its electrical and chemical properties and can be controlled by various reduction methods like thermal, chemical and optical. However, a method with sufficient controllability to regulate the reduction process has been missing. In this work, a hybrid method of thermal and joule heating processes is demonstrated where a progressive control of the ratio of various functional groups can be achieved in a localized area. With this precise control of carbon-oxygen ratio, negative differential resistance (NDR) is observed in the current-voltage characteristics of a two-terminal device in the ambient environment due to charge-activated electrochemical reactions at the GO surface. This experimental observation correlates with the optical and chemical characterizations. This NDR behavior offers new opportunities for the fabrication and application of such novel electronic devices in a wide range of devices applications including switches and oscillators.

摘要

氧化石墨烯(GO)中各种官能团的比例与其电学和化学性质直接相关,并且可以通过热、化学和光学等各种还原方法进行控制。然而,一直缺少一种具有足够可控性来调节还原过程的方法。在这项工作中,展示了一种热加热和焦耳加热过程的混合方法,通过该方法可以在局部区域实现对各种官能团比例的逐步控制。通过对碳氧比的精确控制,由于在GO表面发生的电荷激活电化学反应,在环境条件下的两终端器件的电流-电压特性中观察到了负微分电阻(NDR)。这一实验观察结果与光学和化学表征相关。这种NDR行为为这类新型电子器件在包括开关和振荡器在内的广泛器件应用中的制造和应用提供了新的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbae/5940784/952755f9cb61/41598_2018_22355_Fig1_HTML.jpg

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