Green activation using reducing agents of carbon-based 3D printed electrodes: Turning good electrodes to great

被引:63
|
作者
Redondo, Edurne [1 ]
Munoz, Jose [1 ]
Pumera, Martin [1 ,2 ,3 ,4 ]
机构
[1] Brno Univ Technol, Cent European Inst Technol, Future Energy & Innovat Lab, Purkynova 123, Brno 61200, Czech Republic
[2] Mendel Univ Brno, Dept Chem & Biochem, Zemedelska 1, CZ-61300 Brno, Czech Republic
[3] China Med Univ, China Med Univ Hosp, Dept Med Res, 91 Hsueh Shih Rd, Taichung, Taiwan
[4] Yonsei Univ, Dept Chem & Biomol Engn, 50 Yonsei Ro, Seoul 03722, South Korea
关键词
3D printed electrodes; Additive manufacturing; Polylactic acid; Graphene; Sodium borohydride;
D O I
10.1016/j.carbon.2021.01.107
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
3D printing of carbon-based nanocomposites, which combine the electrical properties of carbon additives with the benefits of thermoplastics, has emerged as a promising route towards rapid and low-cost manufacturing of customised-shaped electronic devices with minimised waste. However, their poor electrical activity in their pristine state makes activation post-treatments mandatory to reduce the amount of insulating polymer. These post-treatments typically involve the use of toxic organic solvents or costly thermal annealing methods. Herein, a simple eco-friendly wet-chemical post-treatment is presented for the quick and general activation of carbon-based 3D printed electronic devices by employing reducing agents like ascorbic acid or sodium borohydride. We tested a range of reducing agents, such as sodium borohydride, lithium aluminium hydride, hydrazine and ascorbic acid, as well as a model oxidising agent like hydrogen peroxide. We found that ascorbic acid and sodium borohydride are the most effective chemicals to achieve electrically active devices while preserving the shape and structure of the 3D printed carbon objects. Thus, this work allows the development of advanced carbon-based 3D printed electrodes by employing an eco-friendly activation approach. (C) 2021 Published by Elsevier Ltd.
引用
收藏
页码:413 / 419
页数:7
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