Application Of Electrode Research Articles

Hydrothermally synthesised α-MnO2 and β-MnO2 nanorods for pseudocapacitor electrode applications

Hydrothermally synthesised α-MnO2 and β-MnO2 nanorods for pseudocapacitor electrode applications

A Stretchable Conductive Material with High Fatigue Resistance for Strain Sensors.

Intrinsically stretchable conductive materials based on elastic substrates and conductive components play important roles in biomedical applications, such as exercise rehabilitation monitoring and disease prediction. A persistent challenge is to combine high fatigue resistance with excellent mechanical properties in stretchable conductive materials. Herein, we present a stretchable conductive material with both good fatigue resistance and high tensile properties (∼3170%) based on poly(acrylic acid)-phytic acid-trehalose-polypyrrole (denoted as PPTP). The as-prepared PPTP hydrogel electrode showed no obvious cracking or delamination after 400 loading and unloading cycles and maintained good electrical signal transmission function after 1000 cycles. We further collected stable signals for human motion and handwriting using the stretchable hydrogel electrode as a strain sensor, demonstrating the potential application of the PPTP stretchable hydrogel electrode in biomedicine.

Electrochemical Methods for Nutrient Removal in Wastewater: A Review of Advanced Electrode Materials, Processes, and Applications

In response to the increasing global water demand and the pressing environmental challenges posed by climate change, the development of advanced wastewater treatment processes has become essential. This study introduces novel electrochemical technologies and examines the scalability of industrial-scale electrooxidation (EO) methods for wastewater treatment, focusing on simplifying processes and reducing operational costs. Focusing on the effective removal of key nutrients, specifically nitrogen and phosphorus, from wastewater, this review highlights recent advancements in electrode materials and innovative designs, such as high-performance metal oxides and carbon-based electrodes, that enhance efficiency and sustainability. Additionally, a comprehensive discussion covers a range of electrochemical methods, including electrocoagulation and electrooxidation, each evaluated for their effectiveness in nutrient removal. Unlike previous studies, this review not only examines nutrient removal efficiency, but also assesses the industrial applicability of these technologies through case studies, demonstrating their potential in municipal and industrial wastewater contexts. By advancing durable and cost-effective electrode materials, this study emphasizes the potential of electrochemical wastewater treatment technologies to address global water quality issues and promote environmental sustainability. Future research directions are identified with a focus on overcoming current limitations, such as high operational costs and electrode degradation, and positioning electrochemical treatment as a promising solution for sustainable water resource management on a larger scale.

Walnut shell/phenolic resin carbon electrodes via laser sintering and KOH activation

Currently, the application of 3D-printed biomass-based carbon electrodes is hindered by their suboptimal performance. This study utilizes walnut shell powder as a carbon source and employs Selective Laser Sintering (SLS) technology for the efficient 3D printing of a double-helix carbon precursor. High-performance biomass-based carbon electrodes are prepared through carbonization and KOH activation. Comparative studies on the microstructure and electrochemical performance of the carbonized and activated samples were conducted. Experimental results demonstrate that KOH activation significantly enhances the microstructure of the carbon electrodes, leading to marked improvements in their electrochemical performance. During desalination experiments, the carbon electrodes exhibited excellent ion removal efficiency, with a maximum conductivity reduction rate of 0.2 μS/cm·min, confirming their feasibility in seawater desalination applications. This research validates the potential of walnut shell biomass for the preparation of 3D-printed carbon electrodes, addressing bottlenecks in traditional carbon electrode manufacturing processes while promoting efficient biomass utilization and environmental protection.

Ce-doped NiFe-layered-double-hydroxide hierarchical nanocomposite and metal/imidazolate framework carbon nanotube nanocomposite: A bifunctional material for OER electrocatalyst and supercapacitor electrode applications

The development of nanocomposites as electrocatalysts with low cost and high efficiency for OER and as electrode material enhancing the electrochemical performance of supercapacitors are the most popular investigations in this field. Herein, a new bifunctional composite including Ce-doped NiFe-LDH Nanosheets and ZIF-derived carbon base incorporating neodymium and Fe into the structure of Zeolitic Imidazolate Framework is proposed and the construction was through entering Fe-ZIF8@Nd-ZIF67 into the structure of NiFeCe-LDH in different ratios of 10, 20 and 30 %. Various physical and electrochemical tests were conducted to evaluate the nanocomposites. Results indicated that the composite presented a hierarchical porous structure and exhibited outstanding performance for OER and supercapacitor applications. According to the results, the 30 % composite of NiFeCe-LDH/ Fe-ZIF8@Nd-ZIF67 exhibits a superior onset overpotential of 170 mV and an overpotential of 300 mV at a current density of 10 mA·cm−2. Besides, it shows an excellent specific capacitance of 345.36 (F.g−1) at 1 A.g−1. Hence, the synthesized nanocomposite demonstrated outstanding performance in both OER and supercapacitor applications.

Evaluation of simplified wireless EEG recordings in the neurological emergency room.

In the neurological emergency room (nER), timely electroencephalography (EEG) diagnostic is often crucial in patients with altered state of consciousness as well as in patients presenting with a first seizure. Yet, routine-EEG (rEEG) is often not available, especially during off-hours. We analyzed the value of a commercially available, simplified wireless eight-channel EEG recording (swEEG, CerebAir® EEG headset, Nihon Kohden), applied by non-EEG-specialized medical students, in patients presenting in our nER with (suspicion of) epileptic seizures and/or loss of or altered state of consciousness between 08/2019 and 08/2022. We evaluated the feasibility and validity compared to a standard rEEG (21 electrodes according to the international 10/20 system) and also included the clinical follow-up of the patients. 100 patients were included in our analysis (mean age 57.6 ± 20.4 years; 61 male). Median time of electrode application was 7 minutes (range 4-20 minutes), with significantly longer duration in patients with altered level of consciousness (median 8 minutes, p = 0.035). Electrode impedances also differed according to state of consciousness (p = 0.032), and were higher in females (p<0.001). 55 patients received additional rEEG, either during their acute nER stay (25) and/or during the next days (38). Considering normal EEG findings vs. pathological slowing vs. epileptiform activity, swEEG matched first rEEG results in 48/55 cases (87.3%). Overall, swEEG detected the same or additional pathological EEG patterns in 52/55 cases (94.5%). In 7/75 patients (9.3%) who did not receive rEEG, or had their rEEG scheduled to a later time point during their hospital stay, swEEG revealed important additional pathological findings (e.g. status epilepticus, interictal epileptiform discharges), which would have triggered acute therapeutic consequences or led to further diagnostics and investigations. The introduced swEEG represents a practicable, valuable technique to be quickly applied by non-EEG-specialized ER staff to initiate timely diagnostic and guide further investigations and treatment in the nER. Moreover, it may help to avoid under-diagnostic with potentially harmful consequences caused by skipped or postponed regular 10/20 EEG examinations, and ultimately improve the outcome of patients.

A simple synthesis of bio-based cathode catalyst of microbial fuel cell with bio-oil recovery through pyrolysis of defatted yeast-biomass

Biomass of plant, yeast and bacterial origin is a promising source of activated biochar or carbon for electrode and catalytic material applications, as it is abundant, diverse, and inexpensive. In this work, the defatted biomass of Meyerozyma caribbica, an oleaginous yeast, was used as the feedstock for biochar production. Activated yeast biochar that was synthesized by using KOH in a single-step one-pot process carried out at 700 °C was found to have a honeycomb-like structure with a surface area of around 412 m2/g. The porous activated-biochar exhibited good electrical properties when applied as a cathode-catalyst material of a microbial fuel cell (MFC). Both coulombic and COD removal efficiencies increased by 1.9 and 1.3 times, respectively, as compared to bare carbon-felt as the cathode. In contrast, the internal resistance of the MFC using activated-biochar-based cathode decreased by 2.6-fold as compared to MFC using carbon felt as cathode. The investigation suggested that defatted yeast-based modified bio-charcoal could be a promising carbon-enriched biomaterial for synthesizing cathode catalyst for application in MFCs. This one-pot process of synthesizing cathode catalyst is based on a net zero-discharge approach with concomitant bio-oil recovery.

Characterization of green-synthesized carbon quantum dots from spent coffee grounds for EDLC electrode applications

This study investigates the green synthesis of carbon quantum dots (CQDs) from spent coffee grounds using a hydrothermal method, offering an eco-friendly, cost-effective, and straightforward approach to nanomaterial production. The synthesized CQDs, with particle sizes ranging from 1.6 to 4.4 nm, exhibited notable fluorescence, achieving quantum yields of 37.0 %, 54.3 %, and 63.3 % depending on the coffee source. Characterization technique, including XRD, FTIR, SEM, TEM, and BET, confirmed their structural suitability of these CQDs for energy storage applications. Their electrochemical performance was evaluated through cyclic voltammetry (CV), galvanostatic charge-discharge (GCD), and electrochemical impedance spectroscopy (EIS). Among the CQDs tested, those derived from spent Liberica coffee ground (medium roasted) demonstrated superior performance, with a discharging specific capacitance of 97.5 F/g, an energy density of 4.3 Wh/kg, and a power density of 130.6 W/kg at a current density of 0.5 A/g. Additionally, they exhibited acceptable internal resistance (Ra = 0.01 kΩ and Rab = 16.9 kΩ), indicating favourable charge transfer characteristics. These results underscore the enhanced energy storage potential of CQDs derived from spent coffee grounds. The findings not only highlight the excellent electrochemical performance but also support the viability of biomass waste as a valuable resource for advanced energy storage applications, promoting sustainable, eco-friendly technologies.

Developing Screen-Printing Processes for Silver Electrodes Towards All-Solution Coating Processes for Solar Cells.

In recent years, third-generation solar cells have experienced a remarkable growth in efficiency, making them a highly promising alternative energy solution. Currently, high-efficiency solar cells often use top electrodes fabricated by thermal evaporation, which rely on high-cost and high energy-consumption vacuum equipment, raising significant concerns for mass production. This study develops a method for fabricating silver electrodes using the screen-printing process, aiming to achieve solar cell production through an all-solution coating process. By selecting appropriate blocking-layer materials and optimizing the process, we have achieved device efficiencies for organic photovoltaics (OPVs) with screen-printed silver electrodes comparable to those with silver electrodes fabricated by thermal evaporation. Furthermore, we developed a method to cure the silver ink using near-infrared (NIR) annealing, significantly reducing the curing time from 30 min with hot air annealing to just 5 s. Additionally, by employing sheet-to-sheet (S2S) slot-die coating, we scaled up the device area and completed module development, successfully verifying stability in ambient air. We have also extended the application of screen-printed silver electrodes to perovskite solar cells (PSCs).

Synthesis of CuS and CuS/C-150 for application in battery type electrode and analysis via electrochemical impedance spectroscopy

Synthesis of CuS and CuS/C-150 for application in battery type electrode and analysis via electrochemical impedance spectroscopy

Biodegradable, Self‐Adhesive, Stretchable, Transparent, and Versatile Electronic Skins Based on Intrinsically Hydrophilic Poly(Caproactone‐Urethane) Elastomer

In biomedical sciences, there is a demand for electronic skins with highly sensitive tactile sensors that have applications in patient monitoring, human–machine interfaces, and on‐body sensors. Sensor fabrication requires high‐performance conductive surfaces that are transparent, breathable, flexible, and easy to fabricate. It is also preferable if the electrodes are easily processable as wastes, for example, are degradable. In this work, the design and fabrication of hydrophilic silanol/amine‐terminated poly(caprolactone‐urethane) (SA‐PCLU) elastomer‐based breathable, stretchable, and biodegradable electrodes are reported. Ag nanowires dispersed in water are sprayed onto the intrinsically hydrophilic electrospun SA‐PCLU that became embedded into the scaffold and formed conformal hydrophilic polyurethane‐based conductive networks (HPCN). The electrodes are used to fabricate capacitive, curvature, and strain sensors, all having monomaterial composition. In addition to displaying particularly good transparencies at low sheet resistances, stretchability, hydrophilicity, and tight and conformal bonding with the target surface, the electrodes also allow the evaporation of perspiration, making them suitable for epidermal sensors for long‐time use. The application of the HPCN electrodes in flexible electronics and bionic skin applications is demonstrated through gesture monitoring experiments and swelling sensors.

Application of Recycled Battery-Graphite Electrode Decorated with Polyglutamic Acid/Au Nanoparticles for Detection of Nalbuphine Drug Abuse

Abstract We report a highly-uniform nanocomposite of polyglutamic acid (PGA) and gold nanoparticles (AuNPs) electrodeposited on a recycled battery graphite electrode (BGE) for the detection of Nalbuphine (NB), a semi-synthetic opioid. The sensor was optimized and characterized morphologically (via scanning electron microscopy, atomic force microscopy, and energy dispersive X-ray analysis) and electrochemically (via cyclic voltammetry, differential pulse voltammetry, and electrochemical impedance spectroscopy). Under optimized conditions, the PGA/AuNPs/BGE revealed two linear ranges, 2.5×10-8 to1.0×10-6 M, and 2.0 × 10-6 to 1.0 × 10-4 M for Nalbuphine (NB), that is equivalent to 9.825×10-3 to 0.393 µg/mL and 0.786 to 39.30 µg/mL, with R2 = 0.995 and 0.994, respectively, and showed good catalytic activity for the determination of nalbuphine in the presence of tramadol and the oxidation potential of these opioid analgesic drugs were separated. The sensor was successfully applied for the detection of NB in its pharmaceutical formulations, spiked urine, and human plasma samples, without applying any sample pretreatment, at a recovery range of 99±0.03 to102±0.02% and thus, the developed can be considered as a promising approach for NB abuse testing in clinical and forensic agencies.

Computational Design of Hydrogenated Monolayer Pyrite for Enhanced Energy Storage

AbstractIn the search for clean energy technologies, it is crucial to develop low‐cost batteries with enhanced performance, and 2D materials are promising for electrode applications owing to their high surface area where fast ionic diffusion can occur. In this work, density functional theory calculations that demonstrate the great potential of recently synthesized 2D pyrite as a battery electrode are reported. An extensive analysis of its performance toward Li‐ion batteries and post‐lithium technologies (Na, K, Mg, Ca, Zn, Al), as well as how point defects can be leveraged to engineer its electronic properties are reported. First, the results explain that the main drawback of the unmodified material, namely its voltammetric peaks at high voltages, is due to the overly strong adsorption of lithium ions. Second, it is demonstrated that hydrogenation of the material leads to milder open‐circuit voltages without compromising the capacity of the anode, and lowers the diffusion barrier to only 0.06eV for both Li and K ions. With a capacity as high as 1317 mAh g−1 for Al‐ion, hydrogenated monolayer pyrite is demonstrated to be a promising material for energy storage applications.

Enhanced Oxidation Resistance and Interface Stability of Atomic-Layer-Deposited MoNx Electrodes via TiN Passivation for DRAM Cell Capacitor Applications.

The continuous miniaturization of dynamic random-access memory (DRAM) capacitors has amplified the demand for electrode materials featuring specific characteristics, such as low resistivity, high work function, chemical stability, excellent interface quality with high-k dielectrics, and superior mechanical properties. In this study, molybdenum nitride (MoNx) films were deposited using a plasma-enhanced atomic layer deposition (PEALD) employing bis(isopropylcyclopentadienyl)molybdenum(IV) dihydride and NH3 plasma for DRAM capacitor electrode applications. Depending on the deposition temperatures of the PEALD MoNx films ranging from 200 to 400 °C, the Mo/N ratio and crystal structure varied, transitioning from the cubic NaCl-B1-type MoN phase with Mo/N ratio of 1.4 to the cubic γ-Mo2N phase with Mo/N ratio of 1.9. Notably, MoNx films grown at 400 °C exhibited low resistivity (435 μΩ·cm), a high work function (5.28 eV), and superior mechanical hardness (11.3 GPa) compared to ALD TiN films. Despite these excellent properties, the PEALD MoNx electrode demonstrated insufficient chemical stability, particularly in terms of oxidation resistance and interface quality with ALD HfxZr1-xO2 (HZO) films. This resulted in poor morphology and the formation of significant oxygen-deficient HZO layers (such as HfO2-x), leading to considerable degradation in the electrical performance of metal-insulator-metal (MIM) capacitors. To mitigate this issue, a thin (2.5-14 nm) ALD TiN layer was introduced as a passivation layer between the MoNx bottom electrode and HZO dielectric. The TiN-passivated MoNx (TiN/MoNx) electrode showed substantially enhanced oxidation resistance and reduced interfacial reactions with the HZO dielectric. Consequently, MIM capacitors with TiN/MoNx bottom electrodes demonstrated outstanding electrical performance, including excellent dielectric properties, low leakage current density, and high mechanical strength. Hence, this study proposes a promising candidates for storage nodes in the next-generation DRAM capacitors.

Corrosion-resistant titanium-based electrodes synergistically stabilized with polymer for hydrogen evolution reaction

The economic and reasonable design of highly stable and corrosion-resistant electrodes is fundamental to achieving the industrial-scale hydrogen productions via water electrolysis, but electrodes’ premature failures are often caused by corrosion and stress damage. Therefore, these challenges are successfully solved by utilizing conductive and crack-resistant polyaniline “stabilizer” with a mild chemical plating process to construct the catalytic electrode on a titanium substrate (15 %PANI-NiB@Ti) in the present work. The 15 %PANI-NiB@Ti catalytic electrodes have been in continuous operation for 350 h at the current density of 200 mA cm−2 with the high efficiency of 98.4 % in a 323.15 K environment. With the high economy and universality, the catalytic electrodes have good catalytic performance and reliability in the extreme industrial environments, such as high temperature, air, and high current density. Except for the above advantages, the 15 %PANI-NiB@Ti catalytic electrodes also have good cracking resistance, which provides a novel and feasible approach to the industrial application of transition metal catalytic electrodes.

Electronic, Optical and Thermoelectric Properties of Two-Dimensional Molybdenum Carbon Mo2C-MXenes

We investigate the structural, electronic, optical, and thermoelectric properties of three compositions of Mo2C-MXenes (Mo2CF2, Mo2C(OH)2, and Mo2CO2) from monolayer to multilayer by first principles calculation within Density Functional Theory (DFT) and Boltzmann transport theory. Firstly, the atomic structures of Mo2C-MXenes are optimized, and their respective structures are created with comparative research. Secondly, their electronic band structures and optical properties are studied in detail. The estimation of the bandgap energy of Mo2C-MXenes with its functionalization reveal that most Mo2CF2 and Mo2C(OH)2 layers are semiconductors, while Mo2CO2 behaves as a metal. The electrical and optical properties can be altered by controlling the on-surface functional groups and the number of layers. Computation of the thermoelectric (TE) properties of Mo2C-MXenes reveals that, upon heating to 600 K, Mo2CF2 and Mo2C(OH)2 exhibit a high Seebeck coefficient and a relatively high electrical conductivity. The Seebeck coefficient reaches ~400 µV K−1 at room temperature for all layers of Mo2CF2 MXenes. Our results prove that Mo2CF2 is considered a promising material for thermoelectric devices, while Mo2CO2 does not possess better thermoelectric performance. Mo2C-MXenes from monolayer to multilayer have outstanding properties, such as flexible bandgap energy and high thermal stability, making them promising candidates for many applications, including energy storage and electrode applications.

Exploring Mo2B MBene as a high-capacity anode material for multi-valent metal-ion batteries: Insights from first-principles calculations

A novel class of 2-dimensional (2D) materials, known as MBenes, has recently been proposed as a promising candidate for electrode applications in metal-ion batteries due to their high conductivity and rich chemistry. In this study, we present a computational investigation into the potential of Mo2B MBene as an anode material for Na-, Mg-, and Al-ion batteries. Using density functional theory (DFT) calculations, we examine the structural, electronic, and electrochemical properties of both H- and T-type configurations of Mo2B. Our findings reveal that Mo2B exhibits metallic behavior and excellent metal adsorption characteristics, with Al exhibiting the strongest binding affinity, followed by Mg and Na. This strong binding, especially with Al, although results in higher diffusion barriers, it enhances layer adsorption leading to increased theoretical capacity. The calculated maximum capacities are significant, with Al (1323 mAh g−1) showing the highest capacity, followed by Mg (923 mAh g−1) and Na (216 mAh g−1). Additionally, the open-circuit voltage (OCV) for all metals ranges between 0.1 and 1.0 V, suggesting the suitability of Mo2B MBene as an anode material that minimizes dendrite formation risks. These results indicate the potential of Mo2B for high-performance multi-valence ion batteries, with particular promise for Al-ion batteries due to their superior capacity. Furthermore, we propose that strain engineering could optimize Mo2B for enhanced performance in Na-ion batteries. Overall, this study suggests Mo2B MBene as a highly promising anode material for next-generation metal-ion batteries, offering significant advantages in terms of capacity, voltage, and safety. Our findings provide insights that could be used for further experimental design of Mo2B-based anodes for energy storage technologies.

Selective electro-induced reduction using bionic BC@SA-Nafion particle electrodes in 3D systems and phytotoxicity assessment

Three-dimensional electrode technology (3D technology), featuring dispersed particulate electrodes is rapidly advancing in the separation of pollutants. However, in contrast to the electrochemical oxidation performance, the design of particulate electrodes for electrochemical reduction remains relatively underexplored. This study introduced a bionic particle electrode (BC@SA-Nafion) with high reducibility and selectivity, and integrated it into a 3D system. Specifically, the selective electro-induced reduction capacity of BC@SA-Nafion was examined using Cr(Ⅵ) as a model pollutant. The electrochemical reactivity of BC@SA-Nafion was found to be dependent on the amount of biochar (BC) incorporated. Furthermore, the selectivity for Cr(Ⅵ) could be fine-tuned by adjusting the Nafion content, thereby addressing the efficiency decline at lower Cr(Ⅵ) concentrations. In the 3D system, the Cr(Ⅵ) removal rate reached up to 99 % under optimal conditions (pH 2, 2 V cm−1, 30 min). The density functional theory calculations indicated that the selectivity of BC@SA-Nafion for Cr(Ⅵ) was dependent on the presence of fluorine bonds. The reduction of Cr(Ⅵ) mainly relied on direct electron transfer provided, with superoxide (·O- 2) also playing a role. Post-treatment with the 3D technology resulted in negligible phytotoxicity of the wastewater. This study introduced a novel strategy for enhancing the selectivity of particle electrodes, thereby expanding the application of the particle electrode and advancing sustainable water treatment technologies.

Pr6O11 modification effectively enhancing sodium storage for Na3V2(PO4)3 batteries

Na3V2(PO4)3 (NVP) is one of the most promising cathode materials for sodium-ion batteries (SIBs) due to its robust three-dimensional framework, high tunability, and relatively high Na+ intercalation potentials. However, its utility is generally constrained by low conductivity, inefficient charge transfer, and subpar interface kinetics. This work presents an efficient and simple method to address these issues. We innovatively modified the NVP surface with Pr6O11 nanoparticles, a negative temperature coefficient (NTC) thermosensitive material, to enhance interface compatibility with electrolytes and improve conductivity. This modification significantly enhances the overall sodium-ion storage performance. Specifically, the optimized NVP-2 %Pr6O11 electrode exhibits excellent electrochemical properties with the aid of an optimized conductivity network compared to the unmodified NVP. Cycled at an 8C current density, the NVP-2 %Pr6O11 electrode achieves high specific capacities of 102.6 mAh·g−1 at 27 °C and 95.6 mAh·g−1 at 45 °C. After 1000 cycles, the capacity retention rates are 81.18 % and 78.97 %, respectively, significantly higher than the 20.59 % and 14.99 % of pure NVP. In coin full-battery testing, the NVP-2 %Pr6O11 electrode retains 89.76 % capacity after 500 cycles at 8C. In addition, the assembled The NVP-2 %Pr6O11//HC pouch full battery exhibits better sodium-ion storage and thermal safety performance compared to the NVP-SP//HC battery. This simple modification strategy provides an effective insight into the application of NVP electrodes in energy storage.

Inert Liquid Exfoliation and Langmuir-Type Thin Film Deposition of Semimetallic Metal Diborides.

Graphite is one of only a few layered materials that can be exfoliated into nanosheets with semimetallic properties, which limits the applications of nanosheet-based electrodes to material combinations compatible with the work function of graphene. It is therefore important to identify additional metallic or semimetallic two-dimensional (2D) nanomaterials that can be processed in solution for scalable fabrication of printed electronic devices. Metal diborides represent a family of layered non-van der Waals crystals with semimetallic properties for all nanosheet thicknesses. While previous reports show that the exfoliated nanomaterial is prone to oxidation, we demonstrate a readily accessible inert exfoliation process to produce quasi-2D nanoplatelets with intrinsic material properties. For this purpose, we demonstrate the exfoliation of three representative metal diborides (MgB2, CrB2, and ZrB2) under inert conditions. Nanomaterial is characterized using a combination of transmission electron microscopy, scanning electron microscopy, atomic force microscopy, IR, and UV-vis measurements, with only minimal oxidation indicated postprocessing. By depositing the pristine metal diboride nanoplatelets as thin films using a Langmuir-type deposition technique, the ohmic behavior of the networks is validated. Furthermore, the material decomposition is studied by using a combination of electrical and optical measurements after controlled exposure to ambient conditions. Finally, we report an efficient, low-cost approach for sample encapsulation to protect the nanomaterials from oxidation. This is used to demonstrate low-gauge factor strain sensors, confirming metal diboride nanosheets as a suitable alternative to graphene for electrode materials in printed electronics.