MXenes constitute a rapidly growing family of 2D materials that are promising for optoelectronic applications because of numerous attractive properties, including high electrical conductivity. However, the most widely used titanium carbide (Ti3C2T
3D continuous mesoscale architectures of nanomaterials possess the potential to revolutionize real‐time electrochemical biosensing through higher active site density and improved accessibility for cell proliferation. Herein, 3D microporous Ti3C2TXMXene biosensors are fabricated to monitor antibiotic release in tissue engineering scaffolds. The Ti3C2TX‐coated 3D electrodes are prepared by conformal MXene deposition on 3D‐printed polymer microlattices. The Ti3C2TXMXene coating facilitates direct electron transfer, leading to the efficient detection of common antibiotics such as gentamicin and vancomycin. The 3D microporous architecture exposes greater electrochemically active MXene surface area, resulting in remarkable sensitivity for detecting gentamicin (10–1 m
- Award ID(s):
- 1757371
- PAR ID:
- 10482861
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Advanced Materials Technologies
- Volume:
- 9
- Issue:
- 4
- ISSN:
- 2365-709X
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract x ) MXene transparent conductive electrode exhibits insufficient environmental stability and work function (WF ), which impede practical applications Ti3C2Tx electrodes in solution‐processed optoelectronics. Herein, Ti3C2Tx MXene film with a compact structure and a perfluorosulfonic acid (PFSA) barrier layer is presented as a promising electrode for organic light‐emitting diodes (OLEDs). The electrode shows excellent environmental stability, highWF of 5.84 eV, and low sheet resistanceR Sof 97.4 Ω sq−1. The compact Ti3C2Tx structure after thermal annealing resists intercalation of moisture and environmental contaminants. In addition, the PFSA surface modification passivates interflake defects and modulates theWF . Thus, changes in theWF andR Sare negligible even after 22 days of exposure to ambient air. The Ti3C2Tx MXene is applied for large‐area, 10 × 10 passive matrix flexible OLEDs on substrates measuring 6 × 6 cm. This work provides a simple but efficient strategy to overcome both the limited environmental stability and lowWF of MXene electrodes for solution‐processable optoelectronics. -
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Abstract 2D early transition metal carbide and nitride MXenes have intriguing properties for electrochemical energy storage and electrocatalysis. These properties can be manipulated by modifying the basal plane chemistry. Here, mixed transition metal nitride MXenes, M‐Ti4N3Tx(M = V, Cr, Mo, or Mn; Tx= O and/or OH), are developed by modifying pristine exfoliated Ti4N3TxMXene with V, Cr, Mo, and Mn salts using a simple solution‐based method. The resulting mixed transition metal nitride MXenes contain 6–51% metal loading (cf. Ti) that exhibit rich electrochemistry including highly tunable hydrogen evolution reaction (HER) electrocatalytic activity in a 0.5
m H2SO4electrolyte as follows: V‐Ti4N3Tx> Cr‐Ti4N3Tx> Mo‐Ti4N3Tx> Mn‐Ti4N3Tx> pristine Ti4N3Txwith overpotentials as low as 330 mV at −10 mA cm−2with a charge‐transfer resistance of 70 Ω. Scanning electrochemical microscopy (SECM) reveals the electrochemical activity of individual MXene flakes. The SECM data corroborate the bulk HER activity trend for M‐Ti4N3Txas well as provide the first experimental evidence that HER results from catalysis on the MXene basal plane. These electrocatalytic results demonstrate a new pathway to tune the electrochemical properties of MXenes for water splitting and related electrochemical applications. -
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x ) MXene encapsulated in parylene‐C. Ti3C2Tx is a 2D nanomaterial with excellent electrical, electrochemical, and mechanical properties, which forms colloidally stable aqueous dispersions, enabling safe, scalable solutions‐processing. Leveraging the excellent combination of metallic conductivity, high pseudocapacitance, and ease of processability of Ti3C2Tx MXene, the fabrication of gel‐free, high‐density EMG arrays is demonstrated, which are ≈8 µm thick, feature 16 recording channels, and are highly skin conformable. The impedance of Ti3C2Tx electrodes in contact with human skin is 100–1000× lower than the impedance of commercially available electrodes which require conductive gels to be effective. Furthermore, the arrays can record high‐fidelity, low‐noise EMG, and can resolve muscle activation with improved spatiotemporal resolution and sensitivity compared to conventional gelled electrodes. Overall, the results establish Ti3C2Tx ‐based bioelectronic interfaces as a powerful platform technology for high‐resolution, noninvasive wearable sensing technologies. -
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Abstract To advance the MXene field, it is crucial to optimize each step of the synthesis process and create a detailed, systematic guide for synthesizing high‐quality MXene that can be consistently reproduced. In this study, a detailed guide is provided for an optimized synthesis of titanium carbide (Ti3C2T
x ) MXene using a mixture of hydrofluoric and hydrochloric acids for the selective etching of the stoichimetric‐Ti3AlC2MAX phase and delamination of the etched multilayered Ti3C2Tx MXene using lithium chloride at 65 °C for 1 h with argon bubbling. The effect of different synthesis variables is investigated, including the stoichiometry of the mixed powders to synthesize Ti3AlC2, pre‐etch impurity removal conditions, selective etching, storage, and drying of MXene multilayer powder, and the subsequent delamination conditions. The synthesis yield and the MXene film electrical conductivity are used as the two parameters to evaluate the MXene quality. Also the MXenes are characterized with scanning electron microscopy, x‐ray diffraction, atomic force microscopy, and ellipsometry. The Ti3C2Tx film made via the optimized method shows electrical conductivity as high as ≈21,000 S/cm with a synthesis yield of up to 38 %. A detailed protocol is also provided for the Ti3C2Tx MXene synthesis as the supporting information for this study. -
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