Scanning atmospheric plasma for ultrafast reduction of graphene oxide and fabrication of highly conductive graphene films and patterns

被引:75
作者
Alotaibi, Faisal [1 ,2 ]
Tung, Tran T. [1 ,2 ]
Nine, Md J. [1 ,2 ]
Kabiri, Shervin [1 ,2 ]
Moussa, Mahmoud [1 ,2 ]
Tran, Diana N. H. [1 ,2 ]
Losic, Dusan [1 ,2 ]
机构
[1] Univ Adelaide, Sch Chem Engn, Adelaide, SA 5005, Australia
[2] Univ Adelaide, ARC Res Hub Graphene Enabled Ind Transformat, Adelaide, SA 5005, Australia
基金
澳大利亚研究理事会;
关键词
Plasma; Air-plasma; Graphene film; Conductive film; Reduction of graphene oxide; SUPERCAPACITOR; TEMPERATURE; PRESSURE; NITRITE; NITRATE;
D O I
10.1016/j.carbon.2017.10.075
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A new method based on scanning atmospheric plasma for an ultrafast reduction of graphene oxide (GO) and preparation of highly conductive graphene films and patterns is presented. This simple method is shown to provide a direct and scalable fabrication of graphene films on flexible and shaped substrates with a variety of patterns for broad applications. An effective and ultrafast (similar to 60 s) reduction of GO films into highly conductive graphene films at room temperature is demonstrated by this process that is impossible to achieve by conventional wet chemical and thermal reduction process. The software controlled x-y scanning unit allows fabrication of graphene films with variety of patterns on different substrates including glass, plastic, ceramics and metals with complex shapes required for flexible and wearable electronics and devices. Characterization results confirmed that a thin transparent graphene film can be produced with a surface sheets resistance of 22 k Omega/sq at the transparency of 88%, and a thick film (similar to 25 mu m) with a sheet resistance of 186 Omega/sq. A practical application of plasma fabricated graphene films was demonstrated for a supercapacitor devices able to deliver an outstanding volumetric capacitance of 536.55 F/cm(3) at a current density of 1 A/g. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:113 / 121
页数:9
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