Low Sheet Resistance Research Articles

Modification of RuO2 nanosheet microstructure via hydrogen plasma treatment for transparent electrode applications

Although monolayer RuO2 nanosheets exhibit semiconducting characteristics, their conductivity must be improved to enable application in transparent electrodes. In this study, RuO2 nanosheet microstructures are modified through H2 plasma treatment to reduce sheet resistance without deteriorating the optical characteristics necessary for flexible transparent electrode applications. Microstructural and chemical changes in the RuO2 nanosheets are observed using monochromator Cs-corrected high-resolution transmission electron microscopy combined with electron energy loss spectroscopy. Single-crystalline RuO2 nanosheets are transformed into nanometer-sized polycrystalline nanosheets. The phase-transformed polycrystalline RuO2 nanosheets contain newly formed defects such as grain boundaries and O vacancies, which result in lower sheet resistances because these defects provide leakage-current paths in the semiconducting RuO2 nanosheets. These defects are located parallel to the direction of light transmission. Consequently, transparency and haze do not significantly deteriorate after H2 plasma treatment. These results indicate that the H2 plasma creates a more stable O-vacancy row which alters the microstructure of the RuO2 nanosheets. Our results demonstrate that H2 plasma treatment can be widely used to fabricate two-dimensional material-based transparent electrodes.

Development of transparent AZO-Ag-AZO electrodes using Xenon flash lamp annealing and application of transparent OLED

Transparent conductive oxide (TCO) is widely used as an electrode in various electronic devices as well as in the semiconductor and display industries. Among TCOs, indium tin oxide (ITO) is distinguished by its excellent transmittance and low resistivity, and it accounts for 90% of the material used in the TCO industry. However, it is plagued by the continuously increasing cost of indium, poor mechanical strength, and the need for a post-annealing process exceeding 250 ℃.The current study has produced an AZO-Ag-AZO multilayer electrode with high conductivity and transmittance by depositing Ag between the AZO layers as a substitute for ITO. Additionally, to enhance the electro-optical characteristics of the manufactured multilayer electrode, Xenon flash lamp annealing (Xe-FLA) was employed as a post-annealing technique. By selecting optimal Ag thickness, flash lamp voltage, and radiant energy density conditions, an exceptional transparent AZO-Ag-AZO with a low sheet resistance of 10.1 Ω/sq and a high transmittance of 92.63 % was successfully created. Furthermore, to explore the feasibility of using the AZO-Ag-AZO electrode under optimal conditions as an Organic Light-Emitting Diode (OLED) anode, a transparent RED OLED device was fabricated by depositing organic, cathode, and CPL layers on the AZO-Ag-AZO.

Synergistic role of Cl- and Br- ions in growth control and mechanistic insights of high aspect ratio silver nanowires for flexible transparent conductive films.

Silver nanowires (AgNWs) with high aspect ratios are pivotal for the production of flexible transparent conductive films (TCFs). The growth of AgNWs is significantly influenced by the strong affinity of halogen ions for silver ions. This affinity plays a crucial role in the controlled deposition of silver along the nanowire axis. By precisely controlling the concentrations of Cl- and Br- ions, we have successfully synthesized AgNWs with remarkable lengths of 96 μm and diameters of 40 nm, achieving an impressive aspect ratio of 2400. Utilizing density functional theory and molecular dynamics simulations, we investigate the impact of these ions on the growth of AgNWs. Our findings reveal that halogen ions strongly adsorb onto the Ag (100) plane in the radial direction, with Cl- ions promoting anisotropic growth and Br- ions effectively limiting the nanowire diameter, thus achieving high aspect ratio AgNWs. The resulting TCFs exhibit a high transmittance of 95.0% at 550 nm and a low sheet resistance of 14.7 Ω sq-1. Moreover, when integrated into a flexible transparent heater, these TCFs demonstrate a high heating rate of 12.1 °C s-1. The development of AgNWs is poised to significantly enhance the performance and versatility of flexible TCFs.

Towards wearable multifunctional cellulose nanofiber/silver nanowire/graphene oxide film: Electromagnetic protection, antibacterial, and motion monitoring

Strong electromagnetic radiation has seriously threatened human body health due to the rapid development of 5G electronic devices towards millimeter wave. The demand for wearable and antibacterial materials with high-performance electromagnetic protection is very urgent, but still lack reasonable structure design to realize multifunctional structure. Here, a wearable and antibacterial cellulose nanofiber/silver nanowire/graphene oxide (CNF-Ag NWs/GO) hybrid film with a multilayer structure is successfully fabricated by a convenient dip-coating method. Such a multilayer structure is constituted by a flexible CNF substrate, electromagnetic shielding blocks of Ag NWs and encapsulation units of GO. Benefiting from the packaging of GO sheets by the hydrogen bond interaction, a dense Ag NWs conductive network is woven. The resulting film shows extremely low sheet resistance of 0.9 Ω/sq and superior electromagnetic shielding performance of 80 dB in the millimeter wave range (26-40 GHz). Meanwhile, an excellent antibacterial property and a motion monitoring ability with high sensitivity are also acquired. The work realizes a multi-functional integration and provides new insight into the development of wearable electromagnetic protection materials.

UV-curable polymer-treated polydimethylsiloxane substrate for ultrahigh-efficient flexible organic light-emitting diodes

Flexible organic light-emitting diodes (FOLEDs) have developed rapidly and have been successfully implemented in the technology of foldable smartphones. As one of the most promising flexible substrates, polydimethylsiloxane (PDMS) suffers from the drawbacks of low thermal stability and weak interfacial adhesion with the low-cost solution-processed poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) film electrodes. In this work, a UV-curable polymer, Norland Optical Adhesive 63 (NOA63), is proposed to enhance the thermal stability and interfacial adhesion, as well as facilitating the light extraction of PDMS substrate. The PEDOT:PSS electrode film on the NOA63 modified PDMS substrate performs a uniform and smooth surface morphology with a low roughness of 3.1 nm, a high transmittance of 94.7 % at 550 nm wavelength, a low sheet resistance of 160 Ω/sq, and superior mechanical durability even after 18,000 bending cycles. The outstanding characteristics of the PDMS/NOA63 substrate enables the fabrication of an ultrahigh-efficient FOLED with a maximum current efficiency, power efficiency and external quantum efficiency of 230.6 cd/A, 144.9 lm/W and 65 %, respectively. This study paves the way to realize high-performance FOLEDs for wearable electronics in the future.

Hybrid Ag-mesh/Ta-doped TiO2 thin film configuration as a visible and near-infrared transparent electrode

This study focuses on the fabrication of a hybrid Ag-mesh/Ta-doped TiO2 (TTO) electrode that has a low sheet resistance and high transparency in the visible and near-infrared region, thereby holding significant commercialization potential. Here, ∼82 nm thick TTO film is deposited on the glass substrate using radio frequency magnetron sputtering technique, over which Ag mesh is carved using the metal aerosol jet printing method. As compared to TTO, sheet resistance of the entire hybrid configuration is found to show a 2-3 order improvement, with the loss of a mere ∼12 % in the visible and ∼8 % in NIR transmittance. The electronic structure of the Ag/TTO interface demonstrates the formation of an ohmic junction, thereby making it suitable for the fabrication of a network-based transparent electrode. Moreover, the overall functionality and preparation route of this electrode makes it more promising as compared to those of the conventional metal mesh and metal-oxide electrodes.

MXene/Bacterial Cellulose Hybrid Materials for Sustainable Soft Electronics.

This work evaluated bacterial cellulose (BC) as a possible biodegradable soft electronics substrate in comparison to polyethylene terephthalate (PET), while also focusing on evaluating hybrid MXene/BC material as potential flexible electronic sensor. Material characterization studies revealed that the BC material structure consists of nanofibers with diameters ranging from 70 to 140 nm, stacked layer-by-layer. BC samples produced are sensitive to post-treatment with isopropanol resulting in a change of structural and mechanical properties. The viscoelastic properties of the BC substrates have been studied experimentally in comparison with the PET film. Aged BC substrate showcased similar viscoelastic properties stability, while exhibiting better properties above 70 °C, with total storage modulus change of -15% and loss modulus change of 21%. MXenes prepared using the Minimally Intensive Layer Delamination (MILD) method were screen-printed onto BC substrates and PET films to form MXene/BC (MX/BC) and MXene/PET (MX/PET) devices. The electrical properties results showcased different resistive behavior on both BC and PET substrate samples with different impedance moduli. MX/PET presented lower sheet resistance of around 156 Ω·sq-1, while MX/BC was 2733 Ω·sq-1. Finally, the MX/BC and MX/PET devices were subjected to repeatable quasi-static load tests and the piezoresistive sensing behavior of the devices has been reported.

Efficiency Improvement on Indium Tin Oxide Films for Dye-Sensitized Solar Cell Using Oxygen Plasma by Bias-Magnetron RF Sputtering Process

Dye-sensitized solar cells (DSSCs) are among the most widely studied thin-film solar cells because of their cost-effectiveness, low toxicity, and simple fabrication method. However, there is still much scope for replacing current DSSC materials due to their high cost, low volume, and lack of long-term stability. Accordingly, indium tin oxide (ITO)-nanorod films were fabricated by electron (E)-beam evaporation using the glancing angle deposition method in this study. Then, the ITO-nanorod was treated with oxygen plasma via a bias-magnetron radio-frequency (RF) sputtering process to improve the efficiency of DSSCs under a varying gas flow rate of 20, 40, 60, 80, and 100 sccm. The field emission scanning electron microscopy (FE-SEM) investigation of the ITO film structure revealed that the obtained nanorod structures have slightly different diameters. At the same time, an increase in the oxygen flow rate resulted in a rougher film surface structure. In this, the lower sheet resistance was received because of rougher morphology. When comparing the DSSCs efficiency (η) test results, we found that at a gas flow rate of 100 sccm, the highest efficiency value showed 9.5%. On the other hand, the ITO-nanorod without plasma treatment exhibited the lowest η. Hence, plasma technology can be practically applied to improve the η of DSSC devices. This study will be a prototype of a highly advanced solar cell manufacturing method for the solar cell industry.

Damage-free non-mechanical transfer strategy for highly transparent, stretchable embedded metallic micromesh electrodes

Stretchable, flexible, transparent electrodes garner significant research interest as indispensable components of flexible optoelectronic devices. However, frequent mechanical transfers during processing pose a considerable challenge in preparing electrodes of scalable size with superior performance and intact structure. Herein, we present a stretchable embedded metallic micromesh (SEMM) electrode with high optoelectronic and robust mechanical properties. The SEMM electrode is fabricated via a damage-free non-mechanical transfer strategy with the assistance of a bifunctional metal transition layer that serves as both a seed layer during electrodeposition and a sacrificial layer during stripping of the electrode. Consequently, the SEMM electrode features a scalable size and an intact structure. By optimizing the electrodeposition parameters, the SEMM achieves high optical transmittance (∼83 %) and low sheet resistance (0.22 Ω sq−1), with a figure of merit reaching 8600–53 times greater than that of commercial polyethylene terephthalate-indium tin oxide (PET-ITO). Furthermore, the SEMM exhibits excellent mechanical stability, enduring up to 60 % of tensile strain and maintaining almost constant normalized resistance after 20,000 bending cycles. Based on the SEMM, a transparent film heater yields rapid response time, low operating voltage, and fast defogging capability. This non-mechanical transfer strategy offers a compelling approach for enhancing the structural integrity and scalability of stretchable embedded transparent electrodes.

Spray-on electronic tattoos with MXene and liquid metal nanocomposites

Electronic tattoos present appealing forms of wearable devices operated directly on the skin. Although two-dimensional transition metal carbides (MXenes) are promising material choices, their films are susceptible to fracturing when subjected to tensile deformations. This study presents electronic tattoos comprising MXenes and liquid metal microcapsules fabricated by spray deposition onto the skin. The resulting nanocomposite has a low sheet resistance of approximately 2.2 Ω/sq. and can be repetitively deformed to 50 % strain. The enhanced deformability is attributed to the release of liquid metal from the microcapsules upon stretching, facilitating the repair of cracks in the nanocomposite layer. In addition, the nanocomposite conforms to the skin, sticks well, and moves with the body. It is also resistant to friction and sweat, making it suitable for various applications. A bifunctional electronic tattoo has been further developed, showcasing its capability to acquire biopotential signals and deliver electrical stimulation. Our study effectively improves the deformability of MXene-based nanocomposites for electronic tattoos, achieving seamless device integration in the body.

Optimization of Contact Pad Design for Silver Nanowire-Based Transparent Heater to Improve Heating Characteristics.

Transparent heaters are gaining significant attention for applications such as antifog glass, smart windows, and smart farm greenhouses. A transparent heater basically consists of transparent conducting materials that serve as a heating area and contact pad electrode to apply power. To fabricate a transparent heater, materials with excellent light transmittance and low sheet resistance are required. Among various transparent conducting materials, such as Indium Tin Oxide (ITO), carbon nanotube (CNT), graphene, and silver nanowires (AgNWs), AgNWs are particularly favored due to their good electrical, optical, and mechanical properties. However, in order to improve the heating characteristics of transparent heaters, research is essential not only on improving the properties of transparent conducting materials but also on the design of contact pad electrodes that can uniformly improve current distribution. Here, we explore various shapes of contact pad electrodes for AgNW-based transparent heaters to improve current distribution. Shapes such as line, spot, twisted, and parallel-type contact pad electrodes are designed and investigated to optimize overall heating characteristics. We analyze the heating properties of these transparent heaters with various contact pad electrodes, demonstrating how their specific shape and size affect heating characteristics and uniformity. We also investigate the optimal shape of the contact pad electrode to minimize transmission loss through UV-VIS spectroscopy. As a result, we confirm that the shape of the contact pad electrode was important for simultaneously achieving high heating characteristics of 120 °C, good heating uniformity, and over 80% transparency in an AgNW-based transparent heater.

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.

Cr2O3–NiO mixed oxides thin films for p-type transparent conductive electrodes

The Cr2O3–NiO mixed oxides’ thin films were formed by means of the layer-by-layer magnetron sputtering deposition of Cr2O3, NiO, and Cr2O3 layers on c-plane sapphire substrates. These thin-film structures, subjected to subsequent annealing, constituted a combination of the monocrystalline (0001) Cr2O3 and nonordered nickel oxide phase, which was a mixture of NiO and Ni2O3. The annealing at 900 and 1000 °С in air facilitated the diffusion of Ni and Cr atoms into the layers. Varying the annealing time allowed us to control the uniformity of the Ni and Cr distribution, the microrelief of the film surface, the transmittance in the visible region, and the sheet resistance of the Cr2O3–NiO thin-film structures. Thus, the films annealed at 900 °C during 30 min were characterized by a uniform distribution, a relatively weakly developed surface, a low sheet resistance, and the highest Haacke's Figure of Merit of 1.49 × 10–9 Ω–1. The formation of mixed Cr2O3–NiO oxides by the proposed approach was found to be an effective way to improve the performances of Cr2O3 based p-type transparent conductive electrodes.

Flexible MXene/CuNWs/tartaric acid composite fabrics constructed by stacking assembly for electromagnetic interference shielding

With the rapid development of modern communication technology, the exploration of flexible wearable shielding fabrics with exceptional electromagnetic interference (EMI) shielding performance has emerged as an utmost priority to safeguard both human beings and electronic devices from the detrimental effects of electromagnetic radiation. Herein, a scalable multilayer stacking assembly method is proposed to prepare uniform MXene/CuNWs/Tartaric Acid (TA) composites-coated fabrics. MXene, as a new type of material, can achieve higher electron and ion transfer rates. However, it is prone to oxidation in air, leading to poor stability. Benefiting from the synergistic effect of tartaric acid, the MXene/CuNWs/TA-coated fabrics exhibit certain oxidation stability and corrosion resistance, while retaining the inherent flexibility and breathability of natural polymer textiles. Furthermore, the multilayer stacking structure works perfectly with the MXene/CuNWs conductive network, enabling multiple reflections and absorptions of electromagnetic waves internally, thus effectively diminishing energy transmission. The modified fabrics exhibit a low sheet resistance of 3.25 ± 0.12 Ω/sq and a good EMI shielding performance of 41.2 dB at X-band. Therefore, MXene/CuNWs/TA fabrics with high shielding performance are expected to reach their potential in wearable electronic products.

Dressing AgNWs with MXenes Nanosheets: Transparent Printed Electrodes Combining High-Conductivity and Tunable Work Function for High-Performance Opto-Electronics.

High-work function transparent electrodes (HWFTEs) are key for establishing Schottky and Ohmic contacts with n-type and p-type semiconductors, respectively. However, the development of printable materials that combine high transmittance, low sheet resistance, and tunable work function remains an outstanding challenge. This work reports a high-performance HWFTE composed of Ag nanowires enveloped conformally by Ti3C2Tx nanosheets (TA), forming a shell-core network structure. The printed TA HWFTEs display an ultrahigh transmittance (>94%) from the deep-ultraviolet (DUV) to the entire visible spectral region, a low sheet resistance (<15 Ωsq-1), and a tunable work function ranging from 4.7 to 6.0eV. The introduction of additional oxygen terminations on the Ti3C2Tx surface generates positive dipoles, which not only increases the work function of the TA HWFTEs but also elevates the TA/Ga2O3 Schottky barrier, resulting in a high self-powered responsivity of 18mAW-1 in Ga2O3 diode DUV photodetectors, as demonstrated via experimental characterizations and theoretical calculations. Furthermore, the TA HWFTEs-based organic light-emitting transistors exhibit exceptional emission brightness of 5020cd m-2, being four-fold greater than that in Au electrodes-based devices. The innovative nano-structure design, work function tuning, and the revealed mechanisms of electrode-semiconductor contact physics constitute a substantial advancement in high-performance optoelectronic technology.

Flexible and transparent leaf-vein electrodes fabricated by liquid film rupture self-assembly AgNWs for application of heaters and pressure sensors

The leaf veins with hierarchically interconnected network structures have great potential as self-assembly templates for transparent and flexible electrodes. In this paper, a liquid membrane ruptured assisted AgNWs self-assembly method was adopted to obtain conductive veins, which show a low sheet resistance of 3.6Ω/□ and a high transparency of 79 % at a minimal materials waste. The figure of merit of conductive veins was as high as 433Ω-1 and can be further increased by increasing the number of soaking because the light transmittance is nearly immune to the AgNWs layer number. The veins maintained a good electrical conductivity even after bending 10,000 times at a 2 mm radius of curvature and exhibited a good corrosion resistance under harsh conditions. Heaters based on the conductive veins are shown as application examples. A high temperature of 104 °C was achieved at a low voltage of 2 V, which is enough to heat cold water. They still have good heating properties even in the bending state or tensile state. Furthermore, pressure sensors based on the conductive veins were fabricated as examples of wearable devices. The sensor exhibits a high sensitivity of 3.8 kPa−1 in the low-pressure range (0–15 kPa) and 17.4 kPa−1 in the high pressure range (15–50.96 kPa). It can monitor human actions such as finger bending, finger taping, throat swallowing and wrist pulse in real-time, which has promising potential for motion monitoring and information encryption applications.

Highly durable and conductive Korea traditional paper (Hanji) embedded with Ti3C2Tx MXene for Hanji-based paper electronics

Lightweight, low-cost, eco-friendly, and mechanically flexible Ti3C2Tx (MXene) electrodes require for paper electronics. We develop a highly durable and conductive traditional Korean paper (Hanji) covered with MXene for Hanji-based paper electronics. The effective networking of MXene on the cellulose structure of Hanji leads to a highly conductive and flexible Hanji which acts as a multi-functional paper for Hanji-based paper electronics. Owing to the synergetic combination of Hanji and MXene, the as-prepared Hanji/MXene exhibits a low sheet resistance of 0.62 Ohm square−1, and outstanding mechanical stability without breaking the Hanji fibers. To further evaluate the potential of our Hanji/MXene composite, its performance in electromagnetic interference (EMI) shielding, interconnectors, heaters, supercapacitors, and temperature sensor applications is investigated. Shielding and heater paper samples employing Hanji/MXene-based electrodes show an EMI shielding efficiency (EMI SE) of 43.3 dB and saturation temperature of 76 °C at a low voltage of 3 V. Moreover, the Hanji/MXene-based supercapacitors exhibit a capacitance of 139.6 mF cm−2 at a current density of 1 mA cm−2. Furthermore, the Hanji/MXene-based temperature sensors exhibit an effective sensing performance over a wide temperature range. Overall, the successful operation of Hanji-based EMI shielding devices, interconnectors, heaters, supercapacitors, and temperature sensors indicates that Hanji/MXene serves as a promising conductive paper substrate for multi-functional paper electronics.

Optimizing Lasing Parameters for Fabricating an Efficient Flexible Electrothermal Heater Based on Laser-Induced Graphene

This work involved fabrication of an efficient thin film heater from 100 μm thick polyimide (PI) sheet by scribing it using a carbon dioxide lasing machine through optimizing laser power (P), scanning speed (SS), and pulses per inch (PPI). A 15 mm × 15 mm square pattern was designed using CorelDRAW software and scribed in a rastering mode on top of PI with the help of Universal Control Panel (UCP) software of the laser machine. Laser power of 8 %, SS of 4 % and PPI of 1000 were obtained as optimal parameters for producing laser induced graphene (LIG). This LIG exhibited a low sheet resistance of approximately 16.64 Ω/sq and was thermally stable on the PI substrate even after 30 cycles of repeated heating and cooling. The LIG was found to be highly porous with the aid of scanning electron microscope (SEM) and its structure was crystalline from XRD patterns. FTIR was conducted and showed disappearance of functional groups in PI after treatment with the laser beam. Our developed LIG heater showed great electrothermal performance with maximum temperature of approximately 288.7 °C, rate of temperature rise of 107.06 °Cs-1, and time of 1.85 s to reach 63 % of temperature difference at a low input voltage of 6 V with homogeneous temperature distribution seen in the thermal images taken using FLIR camera. This LIG heating element can be placed in confined spaces because of its flexibility, thinness, and lightness. Additionally, its efficient joule heating effect attracts many applications such as seat warmers, anti-fogging equipment, food shelf displays, etc.

High-Performance Red Transparent Quantum Dot Light-Emitting Diodes via Fully Solution-Processed MXene/Ag NWs Top Electrode.

The integration of high-performance transparent top electrodes with the functional layers of transparent quantum dot light-emitting diodes (T-QLEDs) poses a notable challenge. This study presents a composite transparent top electrode composed of MXene and Ag NWs. The composite electrode demonstrates exceptional transparency (84.6% at 620 nm) and low sheet resistance (16.07 Ω sq-1), rendering it suitable for integration into T-QLEDs. The inclusion of MXene nanosheets in the composite electrode serves a dual role: adjusting the work function to enhance electron injection efficiency and enhancing the interface between Ag NWs and the emissive layer, thereby mitigating the common issue of interfacial resistance in conventional transparent electrodes. This strategic amalgamation results in notable improvements in device performance, yielding a maximum current efficiency of 23.12 cd A-1, an external quantum efficiency of 13.98%, and a brightness of 21,015 cd m-2. These performance metrics surpass those achieved by T-LEDs employing pristine Ag NW electrodes. This study offers valuable insights into T-QLED device advancement and provides a promising approach for transparent electrode fabrication in optoelectronic applications.

One-Dimensional ZnO Nanorod Array Grown on Ag Nanowire Mesh/ZnO Composite Seed Layer for H2 Gas Sensing and UV Detection Applications.

Photodetectors and gas sensors are vital in modern technology, spanning from environmental monitoring to biomedical diagnostics. This paper explores the UV detection and gas sensing properties of a zinc oxide (ZnO) nanorod array (ZNA) grown on silver nanowire mesh (AgNM) using a hydrothermal method. We examined the impact of different zinc acetate precursor concentrations on their properties. Results show the AgNM forms a network with high transparency (79%) and low sheet resistance (7.23 Ω/□). A sol-gel ZnO thin film was coated on this mesh, providing a seed layer with a hexagonal wurtzite structure. Increasing the precursor concentration alters the diameter, length, and area density of ZNAs, affecting their performance. The ZNA-AgNM-based photodetector shows enhanced dark current and photocurrent with increasing precursor concentration, achieving a maximum photoresponsivity of 114 A/W at 374 nm and a detectivity of 6.37 × 1014 Jones at 0.05 M zinc acetate. For gas sensing, the resistance of ZNA-AgNM-based sensors decreases with temperature, with the best hydrogen response (2.71) at 300 °C and 0.04 M precursor concentration. These findings highlight the potential of ZNA-AgNM for high-performance UV photodetectors and hydrogen gas sensors, offering an alternative way for the development of future sensing devices with enhanced performance and functionality.