A Fully‐Bioresorbable Nanostructured Molybdenum Oxide‐Based Electrode for Continuous Multi‐Analyte Electrochemical Sensing

Author:

Fernandes Catarina1ORCID,Franceschini Filippo2,Smets Jorid3,Deschaume Olivier4,Rusli Nurul1,Bartic Carmen4,Ameloot Rob3,Baert Kitty5,Ustarroz Jon56,Taurino Irene12

Affiliation:

1. Department of Electrical Engineering (Micro‐ and Nano Systems) KU Leuven – University of Leuven Leuven 3001 Belgium

2. Department of Physics and Astronomy (Semiconductor Physics) KU Leuven – University of Leuven Leuven 3001 Belgium

3. Centre for Membrane Separations, Adsorption, Catalysis, and Spectroscopy (cMACS) KU Leuven – University of Leuven Leuven 3001 Belgium

4. Department of Physics and Astronomy (Soft Matter Physics and Biophysics Unit) KU Leuven – University of Leuven Leuven 3001 Belgium

5. SURF‐Research Group Electrochemical and Surface Engineering VUB – Vrije Universiteit Brussel Brussels 1050 Belgium

6. Chemistry of Surfaces, Interfaces and Nanomaterials (ChemSIN) ULB – Université Libre de Bruxelles Brussels 1050 Belgium

Abstract

AbstractBioresorbable electrochemical sensors remain mostly unexplored despite their ability to provide continuous in situ measurements of critical biomarkers. The primary challenge arises from the direct exposure of the electrodes’ thin metal films to biofluids, which poses difficulties in ensuring both proper operational lifetimes and sensing performance. Molybdenum (Mo) presents itself as a promising biometal due to its uniquely gradual dissolution in biofluids, facilitated by the formation of a slower‐dissolving MoOx surface layer. Consequently, carefully engineered MoOx films can endow transient electrochemical sensors with unparalleled stability during extended operational lifetimes. Herein an unprecedented sensor architecture achieved via the unique pairing of sputtered Mo and MoOx thin films, probed as a pH and dissolved oxygen sensor is reported. Compared to a bare Mo electrode, a bilayer Mo+MoOx electrode subjected to post‐deposition annealing (400 °C, 60 min, N2 environment) displayed a largely improved stability (>24 h) in solution and demonstrated predictable functionality during ongoing film dissolution at 37 °C. Collectively, this work establishes a pioneering strategy for the fabrication of reliable and clinically relevant implantable electrochemical sensors.

Publisher

Wiley

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