Patterning (Electro)chemical Treatment-Free Electrodes with a 3D Printing Pen

电极 制作 纳米技术 玻璃碳 化学修饰电极 电极阵列 熔丝制造 电化学 微流控 材料科学 化学 3D打印 工作电极 光电子学 循环伏安法 复合材料 替代医学 物理化学 病理 医学
作者
Lauro A. Pradela‐Filho,William B. Veloso,Débora N. Medeiros,Renato Soares de Oliveira Lins,Bruno Ferreira,Mauro Bertotti,Thiago R. L. C. Paixão
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:95 (28): 10634-10643 被引量:20
标识
DOI:10.1021/acs.analchem.3c01084
摘要

A simple fabrication method to make electrochemical sensors is reported. The electrodes were fabricated with a commercial filament based on polylactic acid and carbon black (PLA/CB). They were engineered with a three-dimensional (3D) printing pen and poly(methyl methacrylate) template. The optimization parameters included the thickness and diameters of the electrodes. The electrode diameter was restricted by the 3D printing pen's nozzle dimension, and larger diameters generated small cracks on the electrode surface, compromising their analytical signal. The electrode thickness can increase the electrical resistance, affecting their electrochemical response. The fabrication showed reproducibility (RSD = 4%). The electrode surface was easily renewed by sanding the electrodes, making them reusable. Additionally, the proposed sensor provided comparable electrochemical responses over traditional glassy carbon electrodes. Moreover, no (electro)chemical surface treatment was required for sensing applications due to the compromise between the thickness and diameters of the electrodes, effectively translating the filaments' electrical properties to resulting materials. The electrodes' analytical performance was shown for organic and inorganic species, including paraquat, Pb2+, and caffeic acid. As proof of concept, the analytical applicability was demonstrated for total polyphenolic quantification in tea samples. Therefore, this work provides an alternative to fabricating miniaturized electrodes, bringing valuable insights into PLA/CB 3D-printed sensors and opening possibilities for designing electrode arrays. Moreover, the proposed electrodes are promising platforms for paper-based microfluidic systems.
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