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Filter, Flip, and Fabricate: A Wax-Assisted Stamp-Transfer Approach for Flexible Ti3C2Tx MXene Electrochemical
Zaheer Ud Din Babar1,2,3, Andy Bruno1,4, Gabriel Maroli1
1Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and BIST, Campus UAB, Bellaterra, Barcelona 08193, Spain.
Abstract:
Combining additive-free solution processing of MXenes with template-assisted transfer represents an innovative approach for the fabrication of electrochemical sensors. Herein, we introduce a wax-assisted templating and stamp-transfer (WAST) approach to fabricate monolithic MXene transducers. To this end, two configurations were developed: (A) MXene-at-all electrodes, where the working, counter, and reference electrodes were entirely composed of MXene, and (B) MXene working electrodes combined with an Ag/AgCl pseudoreference and carbon counter electrodes. Additive-free MXene inks, at different concentrations and volumes, were filtered onto wax-templated PVDF membranes to form stampable patterns. Voltammetric characterization revealed consistent anodic and cathodic peak currents (Ipa and Ipc) and steady peak-to-peak separation (ΔEp) across three independent batches, indicating excellent reproducibility with Ipa = 87.9 ± 1.7 μA, Ipc = -81.3 ± 1.5 μA, and ΔEp = 255.9 ± 4.6 mV for configuration A, and Ipa = 43.8 ± 0.6 μA, Ipc = -62.8 ± 1.2 μA, with a 3-fold lower peak separation (ΔEp = 87.6 ± 0.9 mV) in the case of configuration B (mean ± SE, n = 15). Primary benchmarking with similar commercial systems signifies the efficacy of WAST-produced transducers to mimic commercial electrode performance and provides a robust alternative to conventional deposition methods. In addition, a proof-of-concept experiment for Hg2+ ion sensing validated its potential for practical applications. The WAST method offers a robust fabrication, configuration choice, and tool-light patterning that can accelerate lab-scale prototyping of stand-alone flexible electrochemical devices.
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