# Filter, Flip, and Fabricate: A Wax-Assisted Stamp-Transfer Approach for Flexible Ti3C2T x  MXene Electrochemical Transducers

**Authors:** Zaheer Ud Din Babar, Andy Bruno, Gabriel Maroli, Syedah Afsheen Zahra, Bartolomeo Della Ventura, Raffaele Velotta, Vincenzo Iannotti, Ruslán Alvarez-Diduk, Arben Merkoçi

PMC · DOI: 10.1021/acsami.5c24165 · ACS Applied Materials & Interfaces · 2026-01-15

## TL;DR

This paper introduces a new wax-assisted method to create flexible MXene-based electrochemical sensors with high reproducibility and performance.

## Contribution

A novel wax-assisted stamp-transfer (WAST) method for fabricating MXene electrochemical transducers with flexible configurations.

## Key findings

- WAST method produced MXene transducers with consistent anodic and cathodic peak currents and low peak separation.
- Configuration B showed a 3-fold lower peak separation compared to configuration A, indicating improved performance.
- The method successfully mimicked commercial electrode performance and demonstrated Hg2+ ion sensing capability.

## 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 (I
pa and I
pc) and steady peak-to-peak
separation (ΔE
p) across three independent batches, indicating excellent reproducibility
with I
pa = 87.9 ± 1.7 μA, I
pc = −81.3 ± 1.5 μA, and ΔE
p = 255.9 ± 4.6 mV for configuration A,
and I
pa = 43.8 ± 0.6 μA, I
pc
= −62.8 ± 1.2
μA, with a 3-fold lower peak separation (ΔE
p = 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.

## Linked entities

- **Chemicals:** Hg2+ (PubChem CID 26623)

## Full-text entities

- **Diseases:** WAST (OMIM:143470)
- **Chemicals:** argon (MESH:D001128), C (MESH:D002244), polymer (MESH:D011108), heavy metal (MESH:D019216), T (MESH:D014316), O (MESH:D010100), OH (MESH:C031356), PVDF (MESH:C024865), Ag (MESH:D012834), Al (MESH:D000535), F (MESH:D005461), WAX (MESH:D014885), Hydrofluoric acid (MESH:D006858), H2 (MESH:D006859), H2O (MESH:D014867), KCl (MESH:D011189), -Ti (MESH:D014025), TiO2 (MESH:C009495), nitrogen (MESH:D009584), at (MESH:D001246), Pt (MESH:D010984), ruthenium (MESH:D012428), HCl (MESH:D006851), C-Ti (MESH:C096521), LiCl (MESH:D018021), AlC 2 MAX (-), AgCl (MESH:C037548), Cl (MESH:D002713), MXene (MESH:C000723374), PET (MESH:D011093), HF (MESH:D006195), Li+ (MESH:D008094)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12862758/full.md

## References

67 references — full list in the complete paper: https://tomesphere.com/paper/PMC12862758/full.md

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Source: https://tomesphere.com/paper/PMC12862758