石墨烯
材料科学
塔菲尔方程
晶体管
场效应晶体管
光电子学
纳米技术
阈值电压
电化学
切换时间
电压
电极
电气工程
化学
物理化学
工程类
作者
Shaorui Li,Chenglin Yu,Yongchao Wang,Ke Zhang,Kaili Jiang,Yayu Wang,Jinsong Zhang
标识
DOI:10.1021/acsami.2c10640
摘要
Graphene field-effect transistors (FETs) have attracted tremendous attention owing to the single-atomic-layer thickness and high electron mobility for potential applications in next-generation electronics. With regards to switching methodology, the electric-field-induced metal-insulator transition offers a new strategy to produce a large on/off current ratio through reversible electrochemical hydrogenation of the graphene channels. Therefore, the performance of such electrochemical graphene FETs greatly relies on the kinetics of hydrogenation reaction. Here, we show that the switching time can be systemically controlled by the applied gate voltages and geometries of graphene channels. The turn-on and turn-off time display an exponential dependence on the gate voltages, manifesting the dominated Tafel-form kinetics of hydrogenation reaction in a two-dimensional limit. Moreover, the turn-off time is inversely proportional to the channel width but independent of the length, while the turn-on time relies on both the width and length, as well as the off-state gate voltage and duration. Our work improves the response time to the magnitude of tens of microseconds and advances the application of graphene-based electronic devices.
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