Nanoparticle Films Research Articles

Ionic Liquid-Assisted Thermal Evaporation of Bimetallic Ag-Au Nanoparticle Films as a Highly Reproducible SERS Substrate for Sensitive Nanoplastic Detection in Complex Environments.

Nanoplastic particles are emerging as an important class of environmental pollutants in the atmosphere that have adverse effects on our ecosystems and human health. While many methods have been developed to quantitatively detect nanoplastics; however, sensitive detection at low concentrations in a complex environment remains elusive. Herein, we demonstrate a greener method to fabricate a surface-enhanced Raman spectroscopy (SERS) substrate consisting of self-assembled plasmonic Ag-Au bimetallic nanoparticle (NP) films for quantitative SERS detection of nanoplastics in complex media. The self-assembly of Ag-Au bimetallic NPs was achieved through thermal evaporation onto a vapor-phase compatible ionic liquid based on deep eutectic solvent over the growth substrate. The finite-difference time-domain simulation revealed that the localized field enhancement is strong in the gaps, which generate uniform SERS "hotspots" in the obtained substrate. Benefiting from highly accessible SERS "hotspots" at the gaps, the SERS substrate exhibits excellent sensitivity for detecting crystal violet with a limit of detection (LOD) as low as 10-14 M and excellent reproducibility (RSD of 5.8%). The SERS substrate is capable of detecting PET nanoplastics with LOD as low as 1 μg/mL and about 100 μg/mL in real samples such as tap water, lake water, diluted milk, and wine. Moreover, we also validated the feasibility of the designed SERS substrate for the practical detection of PET nanoplastics collected from commercial drinking water bottles, and it showed great potential applications for sensitive detection in actual environments.

Gas-Phase Fabrication and Photocatalytic Activity of TiO2 and TiO2-CuO Nanoparticulate Thin Films.

CuO-loaded TiO2 nanomaterials have applications in pollutant degradation via photocatalysis. However, the existing methods of fabricating these nanomaterials involve liquid-phase processes, which require several steps and typically generate liquid waste. In this study, TiO2 and TiO2-CuO nanoparticulate thin films were successfully fabricated through a one-step gas-phase approach involving a combination of plasma-enhanced chemical vapor deposition and physical vapor deposition. The resulting films consisted of small, spherical TiO2 nanoparticles with observable CuO on the TiO2 surface. Upon annealing in air, the TiO2 nanoparticles were crystallized, and CuO was completely oxidized. The photocatalytic activity of TiO2-CuO/H2O2, when introduced into the rhodamine 6G degradation system, was substantially enhanced under both ultraviolet and visible light irradiation. Moreover, this study highlights the influence of pH on the photocatalytic activity; TiO2-CuO/H2O2 exhibited the highest photocatalytic activity at pH 13, with a reaction rate constant of 0.99 h-1 cm-2 after 180 min of visible light irradiation. These findings could facilitate the development of nanoparticulate thin films for enhanced pollutant degradation in wastewater treatment.

Interfacial bonding mechanisms of sintered Cu nanoparticles on different metallization surfaces

Cu nanoparticle sintering bonding is a low-cost die-attach method compared with Ag nanoparticles for power electronic packaging. The joint strength highly depends on the surface metallization of the devices. In present study, the interfacial sintering behavior of copper nanoparticle film (CNF) on different metallizations (Au, Ag, and Cu) was studied. The CNF exhibited a superior shear strength (115 MPa) on Cu substrates when sintered at 250 °C-15 MPa, much higher than that on Ag and Au metallized substrates. The interface connection ratio of bondline-substrate showed the same trend as the shear strength. The neck formation at the bonding interfaces showed no orientation preference. The lateral diffusion of Cu atoms on substrates dominated the sintering bonding, rather than the longitudinal diffusion. The Cu metallization showed much faster lateral diffusion than the Ag and Au metallization, which was confirmed by the neck growth of monolayer nanoparticle sintering and the molecular dynamics (MD) simulation.

Remarkable emission enhancement of CsPbBr3 quantum dots based on an Ag nanoparticle-Ag film plasmonic coupling structure.

All-inorganic halide perovskite quantum dots (QDs) have recently received much attention due to their excellent optoelectronic properties. And their emission properties still need to be improved for further applications. Here, we demonstrated a remarkable emission enhancement of the CsPbBr3 QDs based on an Ag nanoparticle-Ag film plasmonic coupling structure. Through precise control of the gap distance between Ag nanoparticle and Ag film, the localized surface plasmon resonance (LSPR) peak was tuned to match the emission wavelength of the CsPbBr3 QDs. We achieved a 30-fold fluorescence intensity enhancement and a lower lasing threshold, which is 25% of that of the CsPbBr3 QDs without plasmonic coupling structure. It is attributed to that the plasmonic coupling structure exhibits an extremely strong local electric field owing to the coupling between LSPR of Ag nanoparticle and surface plasmon polariton of Ag film. This work provides an effective way to enhance the optical emission of perovskite QDs and promotes the further exploration of on-chip light source.

Sol-gel immobilization of lipase enzyme on FTO modified with silica-zirconia and gold nanoparticles films for design of triglyceride impedimetric biosensor

A novel electrochemical sensing platform was created using the formation of a sequence of films, over a conductive fluorine-doped tin oxide glass (FTO), obtained using the sol-gel method and the dip coating technique. Firstly, thin films of silica-zirconia mixed oxides were deposited, in sequence an ionic silsesquioxane film stabilizing and controlling the size of gold nanoparticles (6.5 ± 2.4 nm) was settled, and after the lipase enzyme, obtained from Candida rugosa, was entrapped into a silica film maintaining its operational stability. The films were characterized by scanning electron microscopy (SEM) with EDX, UV–Vis spectroscopy and X-ray photoelectron spectroscopy (XPS). The thickness of each film on the FTO glass was evaluated by optical profilometry. The presence of the enzyme on the platform was confirmed by cyclic voltammetry with the ρ-nitrophenyl palmitate method. This platform was applied successfully as a biosensor for tributyrin (TB) determination by electrochemical impedance spectroscopy EIS, showing low limit of detection (LD) of 1.86 μmol L−1 and high sensitivity of 5.37 μΩ μmol−1 L. The biosensor presented a low KMapp value of 22.69 μmol L− 1 and the Vmaxapp value of 85.57 μmol L−1 min−1 suggesting that the enzyme, immobilized with this method retained activity promoting a fast enzymatic reaction with the TB.

Mesoscale self-organization of polydisperse magnetic nanoparticles at the water surface.

In this study, we investigated the self-ordering process in Langmuir films of polydisperse iron oxide nanoparticles on a water surface, employing in situ x-ray scattering, surface pressure-area isotherm analysis, and Brewster angle microscopy. X-ray reflectometry confirmed the formation of a monolayer, while grazing incidence small-angle x-ray scattering revealed short-range lateral correlations with a characteristic length equal to the mean particle size. Remarkably, our findings indicated that at zero surface pressure, the particles organized into submicrometer clusters, merging upon compression to form a homogeneous layer. These layers were subsequently transferred to a solid substrate using the Langmuir-Schaefer technique and further characterized via scanning electron microscopy and polarized neutron reflectometry. Notably, our measurements revealed a second characteristic length in the lateral correlations, orders of magnitude longer than the mean particle diameter, with polydisperse particles forming circular clusters densely packed in a hexagonal lattice. Furthermore, our evidence suggests that the lattice constant of this mesocrystal depends on the characteristics of the particle size distribution, specifically the mean particle size and the width of the size distribution. In addition, we observed internal size separation within these clusters, where larger particles were positioned closer to the center of the cluster. Finally, polarized neutron reflectometry measurements provided valuable insights into the magnetization profile across the layer.

Domain-Selective Enzymatic Cross-linking and Etching for Shape-Morphing DNA-Linked Nanoparticle Films.

The highly programmable and responsive molecular recognition properties of DNA provide unparalleled opportunities for fabricating dynamic nanostructures capable of structural transformation in response to various external stimuli. However, they typically operate in tightly controlled environments because certain conditions (ionic strength, pH, temperature, etc.) must be met for DNA duplex formation. In this study, we adopted site-specific enzymatic ligation and DNA-based layer-by-layer thin film fabrication to build shape-morphing DNA-linked nanoparticle films operational in a broad range of environments. The ligated films remained intact in unusual conditions such as pure water and high temperature causing dissociation of DNA duplexes and showed predictable and reversible shape morphing in response to various environmental changes and DNA exchange reactions. Furthermore, domain-selective ligation combined with photoinduced interlayer mixing allowed for the fabrication of unusual edge-sealed double-layered films through midlayer etching, which is difficult to realize by other methods.

A theoretical model to predict the Curie and Neel temperatures of Ni and Fe3O4 nanostructured magnetic materials

A simple and unified model, based on size, shape, and surface effect is reported to estimate the magnetic properties of Ni and Fe3O4 nanomaterials. The relaxation factor, which is the ratio of dangling bonds to an atom's total bonds, is reported in the theory to estimate the properties of magnetic nanomaterials. The Curie temperature is projected to decrease with the decrement in particle size. The particle shape influences the Curie temperature of Ni and Fe3O4 nanoparticles and this effect becomes prominent with the reduction in particle size. The model is extended on the same ground to analyze the Neel temperature of Ni and Fe3O4 nanomaterials. Neel temperature also decreases as particle size decreases. The variation of Curie temperature and Neel temperature is projected for spherical, cubic, wire, and film shaped nanoparticles. It is also observed that the effect of size is more appreciable when the shape changes from cubic to the film of nanoparticles. Although, model predictions are valid throughout the size range of nanoparticles, but more noticeable up to the size of 20 nm. Moreover, the reported model is valid for all conducting and semiconducting crystalline nanostructured materials. Our theoretical calculations are in agreement with the standing experimental data and the simulation results for nanoparticles in varying shapes and sizes.

Gamma Ray-Induced Changes in Polyvinyl Alcohol/Carboxymethyl Cellulose/Cadmium Selenide Nanocomposite Films: Optical Analysis for Optoelectronic Devices

In order to create nanocomposite films (NC) of polyvinyl alcohol, carboxymethyl cellulose and cadmium selenide nanoparticles (PVA/CMC/CdSe), thermolysis and ex-situ casting techniques were used. The microstructure and shape of the CdSe nanoparticles (NP) were characterized with the Rietveld method and transmission electron microscopy (TEM). Rietveld refinement of the x-ray data showed that the prepared CdSe NP had the cubic zinc blend structure with a lattice parameter 6.057 Å. The TEM showed the formation of the dotted shape of CdSe with a particle size around 2 nm, confirming the quantum dot size of the mother phase CdSe. Samples from the prepared PVA/CMC/CdSe films were irradiated with γ radiation doses of 20−150 kGy. The resultant effects of the γ ray irradiation on the optical and color properties of the prepared films were investigated using UV–vis spectroscopy and the International Commission on Illumination (CIE) color difference technique. When the γ dose was increased to 150 kGy, the maximum dose used, the direct and indirect optical band gaps (Eg) decreased. We attribute this decrease to the domination of crosslinking that destroyed the ordered structure and thus increased the amorphous regions. In addition, we used the optical dielectric loss (ε”) to identify the type of microelectronic transition for the PVA/CMC/CdSe NC samples, which was found to be a direct allowed transition. The effect of γ ray irradiation on the absorbance, extinction coefficient, refractive index, dielectric parameters and optical conductivity of the NC samples were studied. The enhancement in the optical properties indicated that the γ radiation is a useful tool that allows the use of the resulting PVA/CMC/CdSe NC in optoelectronic devices. Finally, the color differences between the pristine and irradiated films were estimated. The irradiated PVA/CMC/CdSe NC film exhibited significant color differences relative to the pristine films.

Investigation of biosensing properties in magnetron sputtered metallized UV-curable polymer microneedle electrodes

Direct management and assessment of metal film properties applied to polymer microneedle (MN) biosensors remains difficult due to constraints inherent to their morphology. By simplifying the three-dimensional structure of MNs and adjusting the deposition time, different thicknesses of Au films were deposited on the UV-cured polymer planar and MN substrates. Several properties relevant to the biosensing of the Au films grown on the polymer surfaces were investigated. The results demonstrate the successful deposition of pure and stable Au nanoparticles onto the surface of UV-curable polymer materials. Initially, Au islands formed within the first minute of deposition; however, as the sputtering time extended, these islands transformed into Au nanoparticle films and disappeared. The hydrophilicity of the surface remains unchanged, while the surface resistance of the thin film decreases with increasing thickness, and the adhesion to the substrate decreases as the thickness increases. In short, a sputtering time of 5–6 min results in Au films with a thickness of 100–200 nm, which exhibit exceptional comprehensive biosensing performance. Additionally, MNs made of Au/UV-curable polymers and produced using magnetron sputtering maintain their original shape, enhance their mechanical characteristics, and gain new functionalities. The Au/UV-curable polymer MNs exhibited remarkable electrode performance despite being soaked in a 37 °C PBS solution for 14 days. These discoveries have important implications in terms of decreasing the dependence on valuable metals in MN biosensors, lowering production expenses, and providing guidance for the choice and design of materials for UV-curable polymer MN metallization films.

Morphological and structural defect optimization in CsPbBr3 nanoparticle films for light-emitting electrochemical cells

Crystalline and morphological defects in the perovskite film affect the operation of light-emitting devices. Thus, advanced and scalable fabrication techniques can improve device properties. In this work, we use slot-die coating at ambient conditions, followed by hot air drying, to produce CsPbBr3 light-emitting electrochemical cells. We compare this method to spin-coating and analyze film morphology and optical properties. We reveal that annealing the film on a hot plate increases PLQY and Shockley-Read-Hole lifetime, but worsens film morphology. In contrast, hot air drying during deposition improves morphology but reduces photoluminescence. The slot-die coating shows better results for device fabrication. With InGa and Al top electrodes, we achieve luminance 8100 cd m−2 and 2900 cd m−2 at a 5 V bias, respectively.

3D hotspot engineering and analytes strategy enabled ultrasensitive SERS platform for biosensing of depression biomarker

Nowadays, the diagnose of depression mainly relies on clinical examination while impossible to accurately evaluate the occurrence of depression. Chemical approaches are captivating to analyze stress biomarkers for feedbacking body's endocrine response to stress stimuli. However, it remains challenging in exploring accurate, reliable and sensitive approaches. Herein, we rationally design a newly SERS platform with integrated hotspots engineering and analyte strategy to achieve highly sensitive analysis for estrogen, a typical depression biomarker in adolescent female. On the one hand, the 3D micro/nano plasmonic substrate containing Au–Ag Alloy Nanourchins (AAA-NUs) and arrays-based monolayer films of Au nanoparticles (Au NSs) was constructed to achieve high density and availability of hotspots. On the other hand, the analyte strategy was designed via rapid azotizing reaction to further enhance the scattering cross-section of estrogen in the form of azido compounds. With the synergism of them, the proposed SERS platform displayed high sensitivity for estrogen with a limit of detection down to 10−11 mg/mL. More importantly, the blood estrogen levels of depressed patients were evaluated via the proposed SERS platform and presented high consistence with clinical diagnostic results. This integrated SERS platform paves the way for universal and ultrasensitive biosensing and possess great potential for applying in multi-target detection and disease prediction.

Boosted photothermoelectric effect in silver nanoparticles decorated carbon nanotube films for infrared detection and actuation

Photothermoelectric (PTE) effect provides a platform for utilization both photon and thermal energy, giving rise to high-performance photodetector and radiation energy harvester. Carbon nanotube (CNT)/metal heterojunction has been demonstrated to be capable of boosting power generation based on PTE effect, and yet the responsivity and detectivity are inferior to those based on conventional optoelectronic effect. Herein, CNT films decorated by Ag nanoparticles (NPs) forming Ag/CNT heterojunctions have been investigated, showing both excellent photothermal and power conversion capability under infrared (IR) illumination. Ultrahigh ΔT of 196.4 K, maximum output voltage of 15.74 mV and power of 9.94 μW have been achieved under IR laser illumination at power density of 7.65 W/cm2, which are superior to reported photodetectors based on PTE effect. CNT@Ag NPs film possesses competitive photodetection performance as well, with responsivity and detectivity of 107 mV/W and 947.68 MHz1/2/W, respectively. Furthermore, when integrated with polydimethylsiloxane, an IR laser actuated movement function mimicking caterpillar has been realized. Our study thus expands the diverse functions of CNT-based films utilizing PTE effect toward applications in IR detection, radiation energy harvesting and soft actuation.

Low-temperature iodinated plasmonically tuned Ag@AgI core-shell nanostructured thin films for highly specific ascorbic acid SERS detection at ultra-low concentrations

A simple low temperature iodination route was developed to controllably iodinate silver nanoislands film (Ag) into silver@silver iodide core-shell nanoparticles film (Ag@AgI) as a chemically stable, near infrared active surface enhanced Raman scattering (SERS) substrate. The localised surface plasmon resonance (LSPR) of the core-shell film exhibits a huge red-shift of 100 nm. The formation of Ag core and a complete ultra-thin AgI shell layer on top of the core is confirmed by transmission electron microscope. Selected area electron diffraction reveals the amorphous nature of AgI shell layer. These results are further substantiated by Raman and x-ray diffraction measurements. The enhancement factor of Ag@AgI film estimated with methylene blue is 5 × 106, an order of magnitude higher compared to that of Ag film. It demonstrated excellent chemical stability and unwavering SERS performance for two months since fabrication. The Ag@AgI film fielded as a label-free SERS substrate exhibited a lowest limit-of-detection of 1 × 10−12 M for ascorbic acid and a linear detection range of 1 × 10−6 to 1 × 10−12 M. The ascorbic acid selective signal enhancement of Ag@AgI film at low concentration region offers a practical sample dilution strategy to suppress interference from non-target molecules in biofluids.

THE PREPARATION OF NANOPARTICLE FILMS BASED ON LIGHT WELDING TECHNOLOGY

Continuous improvements in scientific research methods have led to increasingly in-depth technological applications of nanomaterials. Currently, research on nanomaterials is no longer limited to analyzing their physical properties, but also focuses on ways to achieve efficient and low-cost nanomaterial synthesis. Nanoparticle films (NFs) are a type of nanomaterial that can be applied in multiple fields. In this study, we investigated ways to improve the self-assembly technology at the water-vapor interface using light welding (LW) technology in order to enhance the mechanical strength and achieve low-cost nanomaterial preparation of high conductivity and flexible metal NFs. The results showed that the resistance of NFs significantly decreased after improving the self-assembly technology at the water-vapor interface using the LW technology. After 60 minutes of light treatment, the resistance of silver NFs decreased by about 53 Ω and the resistance of the gold NFs decreased by about 9 Ω. After photo-welding treatment, the catalytic activity of the self-supporting porous gold film was the highest with a peak current density of 24.6 μA/cm<sup>2</sup>. The results obtained in this research study can be employed to improve the preparation technology of fluid self-assembled nanomaterials. LW technology can be utilized to achieve low-cost manufacturing of nanomaterials with high strength and expand the application field of NFs.

A changeable critical state for a switchable photocurrent direction via the photo-electrochemical photocurrent polarity switching effect in BiFeO3 nanoparticulate films.

The photoelectrochemical photocurrent switching (PEPS) effect to change the photocurrent direction from cathodic to anodic via external bias is an important phenomenon. Specifically, tuning the critical state or the potential corresponding to a switchable photocurrent direction through easily controllable parameters is crucial for developing efficient photo-electrocatalyst systems. Although the PEPS effect has been reported in quite a few recently published studies, the changeable critical state has not yet been demonstrated. In this study, for the first time, we present a photoelectrochemical (PEC) system based on bismuth ferrite (BiFeO3) nanoparticulate films that demonstrates a changeable critical state controlled via the composition of an electrolyte medium. In particular, the ionic strength (tuned via addition of inert salt) and the concentration of dissolved oxygen in an electrolyte medium are noted to dictate the potential corresponding to the critical state. Importantly, we demonstrate that this potential can be predicted using the Nernst equation by considering electrolyte energy level rearrangement and the kinetic theory of semiconductor electrodes. This study enhances the understanding of carrier transport in PEC activities and enables precise control over the reversal of the photocurrent direction that may pave the way for developing sophisticated multifunctional photoelectric devices and efficient photo-electrocatalyst systems.

Rapid electrodeposition of Cu nanoparticle film on Ni foam as an integrated 3D free-standing electrode for non-invasive and non-enzymatic creatinine sensing.

High cost, inherent destabilization, and intricate fixing of enzyme molecules are the main drawbacks of enzyme-based creatinine sensors. The design of a low-cost, stabilizable, and enzyme-free creatinine sensing probe is essential to address these limitations. In this work, an integrated three-dimensional (3D) free-standing electrode was designed to serve as a non-enzymatic creatinine sensing platform and was fabricated by rapid electrodeposition of a dense copper nanoparticle film on nickel foam (Cu NP film/NF). This low-cost, stable, easy-to-fabricate, and binder-free Cu NP film/NF electrode has abundant active sites and excellent electrochemical performance. Cyclic voltammetry measurements show a wide linear range (0.25-24 mM), low detection limit (0.17 mM), and high sensitivity (306 μA mM-1 cm-2). The developed sensor shows high recovery of creatinine concentration in real urine. Besides, it has better specificity, reproducibility, and robustness in detecting creatinine. These excellent results suggest that a non-enzymatic creatinine sensor based on an integrated 3D free-standing Cu NP film/NF electrode has good potential for non-invasive detection of urinary creatinine.

Impact of water solvation on the charge carrier dynamics of organic heterojunction photocatalyst nanoparticle dispersions.

Organic heterojunction nanoparticles (NP) have recently gained significant interest as photocatalysts for visible light-driven hydrogen production. Whilst promising photocatalytic efficiencies have been reported for aqueous NP dispersions, the underlying dynamics of photogenerated charges in such organic heterojunction photocatalysts and how these might differ from more widely studied dry heterojunction films remain relatively unexplored. In this study, we combine transient optical spectroscopies over twelve orders of magnitude in time, using pulsed and continuous light illumination, to elucidate the differences in the charge carrier dynamics of heterojunction NP dispersions, dried NP films, and bulk heterojunction films prepared by spin coating. The ultrafast fast (ps to ns) transient absorption results show efficient charge generation and indistinguishable nanosecond charge recombination decay kinetics of separated charges in all three samples. In contrast, on the slower μs to ms time range, the decay kinetics of heterojunction NP dispersion exhibited up to 15-fold larger amplitude and more than one order of magnitude slower decay of the photogenerated charges than those in films. The analysis of the nanomorphology, NP surfactant, polymer residual metal content and local polar environment suggest that the longer lifetime differences (in ms) in the charge recombination in NP dispersion are mostly associated with a charge carrier stabilisation on a shallow density of states on the NP surface of ∼350 meV by interaction with local water environment, resulting in suppressed charge recombination. The lengthening of NP dispersion charge carrier lifetime is discussed regarding the energetic loss for function and their implications in photocatalysis.

Bismuth-oxide nanoparticles: study in a beam and as deposited.

Bi2O3 is a promising material for solid-oxide fuel cells (SOFC) due to the high ionic conductivity of some phases. The largest value is reached for its δ-phase, but it is normally stable at temperatures too high for SOFC operation, while nanostructured oxide is believed to have more suitable stabilization temperature. However, to manufacture such a material with a controlled chemical composition is a challenging task. In this work, we investigated the fabrication of nanostructured Bi2O3 films formed by deposition of free Bi-oxide nanoparticles created in situ. The particle-production method was based on reactive sputtering and vapour aggregation. Depending on the fabrication conditions, the nanoparticles contained either a combination of Bi-metal and Bi-oxide, or only Bi-oxide. Prior to deposition, the free particles were probed in the beam - by synchrotron-based photoelectron spectroscopy (PES), which allowed assessing their composition "on the-fly". The nanoparticle films obtained after deposition were studied by PES, scanning electron microscopy, transmission electron microscopy, and electron diffraction. The films' chemical composition, grain dimensions, and crystal structure were probed. Our analysis suggests that our method produced Bi-oxide films in more than one polymorph of Bi2O3.

Tailoring the temperature coefficient of resistance of flame-formed carbon nanoparticle thin films by electric field-assisted deposition

The electric-field assisted deposition is successfully proposed as a method for the manufacturing of carbon nanostructured films with tunable properties, benefiting from the superimposition of electric fields on the thermophoretic deposition. Morphology, optical, and thermo-resistive properties of the carbon nanoparticle (CNP) films have been studied by UV–vis Absorption Spectroscopy, Scanning Electron Microscopy, Atomic Force Microscopy, and Current-Voltage analysis. In comparison to thermophoresis alone, the introduction of an electric field results in a six-fold increase in the deposition rate characterized by a non-linear film growth influenced by a three-fold augmentation in surface roughness and polarization effects. Notably, the surface morphology of the CNP films undergoes modification, exhibiting larger grains and a reduced optical band gap energy. Moreover, while maintaining a non-ohmic behaviour, the electric field plays a crucial role in increasing by about two orders of magnitude the electrical conductance of CNP films at ambient temperature. This effect is accompanied by a decrease in temperature sensitivity, attributed to the low and nearly temperature-independent activation energy for the tunneling of electrons in the percolative network. In summary, electric-field assisted deposition is a promising approach to tailor the thermal response of CNP films, which could be beneficial for the development of next-generation sensors.