Crystallite Surface Research Articles

Plants-extracts mediated CuS nanoparticles: An effective antibacterial agent

Antibacterial activity of plant-mediated synthesized CuS nanoparticles against gram-positive Bacillus subtilis and gram negative Pseudomonas putida is studied in this presented work. A facile hydrothermal approach was followed to synthesize spherical shaped CuS nanoparticles using flowers extract of Tagetes patula (S1), leaves extract of Azadirachta indica (S2), and bark extract of Terminalia arjuna (S3). Crystal phase identification, average crystallites size, surface morphology, absorbance spectra and energy band gap analyses of samples were further determined using XRD, SEM, and UV-DRS spectroscopy respectively. Furthermore, under irradiation of visible light, antibacterial activity of marigold flowers mediated (S1), neem leaves mediated (S2), and arjuna bark mediated (S3) CuS samples were studied. XRD data confirmed the marigold mediated CuS sample has relatively smaller crystallites size of 10.67 nm. The estimated band gap energies for respective S1, S2, and S3 samples are 174 eV, 175 eV, and 177 eV. The antibacterial analysis of S1 sample displays its excellent antibacterial activity with the formation of relatively large inhibition zones of 29 mm and 30 mm diameters, against Bacillus subtilis and Pseudomonas putida respectively. The demonstrated antibacterial activity of biocompatible CuS nanoparticles suggests their potential use in biomedical applications.

Carboxymethyl cellulose assisted morphology controlled synthesis of Mn3O4 nanostructures for adsorptive removal of malachite green from water

The physicochemical properties of manganese oxides and their different applications mainly depend upon their crystallite size, morphology, phase structure, and surface properties, which are again dependent on the preparation methods. So, a simple, cost-effective, and versatile synthesis method for such materials is highly desirable. Intending to accomplish this, herein we report the synthesis of Mn3O4 nanostructures by alkaline hydrolysis of the corresponding metal ions in an aqueous medium. The addition of a biodegradable polymer, sodium salt of carboxymethyl cellulose (Na-CMC) assisted the development of specific morphology, which is tunable by varying the concentration of the biopolymer. The spectroscopic, microscopic, and diffractometric analyses of the synthesized Mn3O4 nanostructures confirm that this particular simple technique is very effective in controlling the morphology of the formed nanostructures. These Mn3O4 nanostructures exhibit excellent adsorption capacity in the removal of malachite green (MG) from its aqueous solution under ambient conditions. The adsorption process is exothermic following pseudo-second-order kinetics with a maximum dye adsorption capacity of 489.68 mg g−1 according to the Sips isotherm model. The Mn3O4 nanostructures can be reused for up to five cycles of dye adsorption without significant loss of their adsorption performance.

Enhanced ammonia gas sensing performance at room temperature of binder-free NiO, Cu and Co-doped NiO thin films synthesized via the SILAR method

We have comprehensively analyzed the influence of Cu and Co-doping on the structural, compositional, optical, and ammonia sensing characteristics of NiO thin films. The X-ray diffraction analysis revealed that pure NiO, Cu, and Co-doped NiO thin films possess a cubic structure. Remarkably, the Co-dopant caused a transformation in the crystallite size and surface structure of NiO. This alteration ultimately enhanced the sensing capabilities of Co-doped NiO thin films. The presence of Co decreased the amount of energy needed to activate Co-doped NiO, resulting in enhanced sensing capabilities of the doped samples for detecting 50 parts per million of ammonia with a response time of 20 s and recovery time of 16 s and having a percentage response of 76.25 %. The enhanced sensor responsiveness and selectivity of the Co-doped NiO sensor towards ammonia can be attributed to its increased surface area, smaller crystallite sizes, and superior surface properties. The remarkable results of Co-doped NiO thin films exhibited show a potential for use in the production of highly efficient ammonia gas-detecting devices.

Exploring Biliverdin's Molecular Interactions with Cu- and Fe-Based MOFs: A Unified In Vitro Study with Photoacoustic Analysis.

Metal-organic frameworks (MOFs) have shown promise in enhancing the stability of biomolecules. Herein, biliverdin (BVD), a photoacoustic (PA) and fluorescent agent, was immobilized within the pores of NH2-MIL-101 (Fe) (FeMOFs) and on the surface of CuBTC crystallites (CuMOFs). MOFs were found to enhance the fluorescence emission and quench the PA intensity of biliverdin. Fluorescence and PA studies, in tandem with DFT simulations, demonstrated that the spectral interactions between MOFs and BVD resulted from interactions between biliverdin and the MOF pores and surfaces in addition to alterations in the HOMO-LUMO energy gap. The MOF internal structure of the MOF played a role in BVD loading, with the FeMOFs enabling greater BVD encapsulation, while CuMOF interactions with BVD primarily took place on the MOF surface. The role of these surface vs pore interactions in the release of biliverdin was explored. This study demonstrates that the effects of the MOF internal structure, surface interactions, and energy interactions should be taken into consideration for biomolecule loading in MOFs.

Supermolecule-opitimized defect engineering of rich nitrogen-doped porous carbons for advanced zinc-ion hybrid capacitors.

Pitch-based porous carbons with adjustable surface chemical property and controllable pore structure are regarded as promising cathode materials for aqueous zinc-ion hybrid capacitors (ZIHCs), while its disordered carbon matrix and microstructure as well as insufficient surface defects often result in low Zn2+-storage capacity and poor rate capability of ZIHCs. Herein, a synergetic strategy of self-assembled supermolecule and enriched defective carbon engineering was developed to achieve ultrahigh edge-nitrogen doping for ZIHCs. The crystallite defects and surface structure of porous carbon could be effectively achieved through grafting electronegative oxygen-containing small molecules and high-level nitrogen-containing functional groups between modified polycyclic aromatic hydrocarbon and supermolecule framework. The optimized three-dimensional carbon structure delivered high capacity of 218 mAh g-1 at 0.2 A g-1, fast charge/discharge capability, enhanced energy density (165.4 Wh kg-1) and superior cycling stability (95% retention after 10000 cycles as cathode of ZIHCs). This provided new insight into the controllable synthesis of carbon cathodes for ZIHCs and expects to prepare functional porous carbon by supermolecules and special precursors.

Ultrasonic-assisted pulse electrodeposition process for producing nanocrystalline nickel films and their corrosion behavior: Competition between mass transport and nucleation

Ultrasonic-assisted pulse electrodeposition of nanocrystalline nickel (NC-Ni) coatings from Watts bath on copper substrate was investigated. Direct (DC), pulsed (PC), and pulse reversed (PRC) current electrodeposition techniques were employed to electrodeposit NC-Ni coatings in the absence and presence of ultrasound wave with a nominal power ranging from 95 W to 200 W and their surface morphology, hardness, and crystalline microstructure were compared. We observed that as the ultrasound power increases, the cathodic efficiency and the microhardness increase, whereas the crystallite size and surface roughness decrease for NC-Ni electrodeposited by the three techniques in the same way. However, the effect of pulse waveform is dominant. The finest crystallite size (24 nm) and highest hardness (585 HV) were achieved for NC Ni coatings PC electrodeposited using an ultrasound with 200 W nominal power. It is believed that the coating produced by PC and PRC techniques develops a preferential orientation in (111) and (100) planes, respectively. The application of ultrasound wave and increasing its nominal power changes the preferential orientation of all obtained coatings to (111) planes. The corrosion behavior of NC Ni coatings, as investigated by potentiodynamic polarization and electrochemical impedance spectroscopy in NaOH solution, demonstrates the effect of nanocrystalline on the passivation and corrosion resistance of NC-Ni coatings.

The impact of the phase composition of bacterial cellulose on the low-temperature mobility of its molecules

We describe the properties of the bacterial cellulose of various origins obtained with the help of XRD, FTIR, and dielectric spectroscopy methods. The samples were produced by Gluconacetobacter bacteria (with Іα phase content of 36%) and a symbiotic culture of bacteria and yeasts present in Kombucha fermented drink (with Іα phase content of 62%). An increase in the Іα phase concentration results in a decrease in the intensity of the low-temperature dielectric relaxation and its shift toward higher temperatures. We demonstrate that this dielectric relaxation occurs primarily due to the reorientation of the methylol groups on the surfaces of the cellulose crystallites. We also report that the concentration of the activated relaxers in Іβ cellulose allomorph exceeds that of the Іα allomorph.

Synthesis and characterization of hydrophobic nickel catalyst supported on different oxides for continuous liquid phase catalytic exchange reaction

Hydrophobic Ni catalysts supported on three metal oxides coated with PTFE namely Ni/SiO2/PTFE, Ni/Cr2O3/PTFE, and Ni/Al2O3/PTFE were used in liquid-phase catalytic exchange (LPCE) reactions to enrich hydrogen isotope and produce deuterium oxide (heavy water). Wet impregnation method was employed to prepare the Ni/SiO2, Ni/Cr2O3, and Ni/Al2O3 before PTFE coating. The as prepared catalysts were characterized using different characterization techniques and their performances were evaluated in LPCE reaction using a continuous reactor. The performance evaluation based on the D2O yield can be ranked as Ni/Al2O3/PTFE > Ni/Cr2O3/PTFE > Ni/SiO2/PTFE > Ni/PTFE. The catalysts’ performances are strongly associated with the crystallite size, particle size, hydrophobicity, surface area, pore size, and metal-support interaction. Since isotope exchange requires a dry catalyst surface, the catalyst’s hydrophobicity plays a crucial role. In addition, the catalyst support improves the LPCE reaction efficiency, as the most efficient catalyst, Ni/Al2O3/PTFE, yielded 1220 ppm D2O, compared to 520 ppm for the benchmark catalyst, Ni/PTFE. The characterization results reveal that Ni/Al2O3/PTFE outperformed the other catalysts due to its low crystallite size (D = 23.04 nm), high hydrophobicity (WCA = 139.23°), higher surface area (16.31 m2g−1), small pores (pore size = 6.18 nm), and lowest average Ni particle size (40.89 nm).

Investigation on antioxidant, antimicrobial, anti-inflammatory, and neuropsychiatry potential of phyto-mediated ZnONPs using Colebrookeaoppositifolia

The present study reports the phyto-mediated synthesis of ZnONPs using methanol extracts and n-Butanol fractions from the roots and leaves of C. oppositifolia. The synthesized nanoparticles were characterized using XRD, FE-SEM, HR-TEM, and XPS techniques to determine their crystallite structure, elemental composition, surface topography, and physio-chemical properties. Furthermore, the biological potential of ZnONPs was evaluated for antioxidant, antimicrobial, anti-inflammatory, and in vitro cytotoxic potential on SH-SY5Y neuroblastoma cell lines. Notably, LEME-ZnONPs exhibited exceptional antioxidant activity with an IC50 of 30.200 μg/mL in the DPPH assay. The antimicrobial efficacy was also remarkable, displaying high maximum activity against bacterial strains, evidenced by zones of inhibition (ZOI) measuring 15.67 ± 0.58 mm (E. coli) and 14.67 ± 0.58 mm (S. aureus) for RTME-ZnONPs, attributable to their small crystallite size. Similarly, against antifungal strains, LEBF-ZnONPs (60.94 ± 0.83 %) and RTBF-ZnONPs (60.85 ± 0.74 %) exhibited potency to inhibit both F. oxysporum and R. necatrix due to their small particle size. Furthermore, LEBF-ZnONPs demonstrated superior anti-inflammatory properties, registering an impressive 98.681 %, outperforming Diclofenac sodium (96.835 %). Importantly, the phyto-mediated ZnONPs exhibited minimal cytotoxicity on SH-SY5Y cell lines at 62.5 μg/mL, a concentration employed as an experimental model to assess neuronal function. The multifaceted applications of phyto-mediated ZnONPs extend across various fields, including pharmaceutical sciences, agriculture, and the treatment of neurological diseases.

Roles of different Ni-Si interactions in methane combustion under oscillating temperature conditions

The silicon- modified nickel oxide catalysts with the same compositions but distinct Ni-Si interactions were obtained via different synthesis routes and utilized for methane combustion under conditions of oscillating temperatures. For catalysts prepared by co-grinding, amorphous SiO2 was dispersed on the surface of large NiO crystallites. During high-temperature calcination or reactions, the crystallization of SiO2, coupled with the sintering or decomposition of NiO crystallites, led to the inferior catalytic activity and stability. Interactions between Ni and Si species were enhanced in catalysts synthesized by precipitation. The Si species was incorporated into the NiO lattice to inhibit the growth of NiO crystallites and to generate nickel silicate species under thermal treatments. The small NiO crystallites provided more Ni3+ and active oxygen species for methane activation and oxidation, while the bulk nickel silicate species played a pivotal role in improving thermal stability, conjointly provoking excellent catalytic performance in cyclic heating–cooling tests between 180 and 800 °C. This study offers new insights into the design of metal oxide composites for catalytic applications.

Decoding Excimer Formation in Covalent-Organic Frameworks Induced by Morphology and Ring Torsion.

A thorough and quantitative understanding of the fate of excitons in covalent-organic frameworks (COFs) after photoexcitation is essential for their augmented optoelectronic and photocatalytic applications via precise structure tuning. The synthesis of a library of COFs having identical chemical backbone with impeded conjugation, but varied morphology and surface topography to study the effect of these physical properties on the photophysics of the materials is herein reported. The variation of crystallite size and surface topography substantified different aggregation pattern in the COFs, which leads to disparities in their photoexcitation and relaxation properties. Depending on aggregation, an inverse correlation between bulk luminescence decay time and exciton binding energy of the materials is perceived. Further transient absorption spectroscopic analysis confirms the presence of highly localized, immobile, Frenkel excitons (of diameter 0.3-0.5nm) via an absence of annihilation at high density, most likely induced by structural torsion of the COF skeletons, which in turn preferentially relaxes via long-lived (nanosecond to microsecond) excimer formation (in femtosecond scale) over direct emission. These insights underpin the importance of structural and topological design of COFs for their targeted use in photocatalysis.

Metal Substitutions (M = Al, Ga, In; Sn, Ge; and Mn, Fe, Co) in ZnS: Sphalerite versus Wurtzite Formation.

A series of Zn1-xMxS polycrystalline samples were synthesized via a solid-state reaction in closed vessels to examine the solubility of foreign M cations within the wurtzite ZnS structure, employing quenching or slow cooling processes to favor specific polymorphs. X-ray diffraction (XRD) and transmission electron microscopy (TEM) analyses revealed diverse structural behaviors across different cations. Group 13 elements (Al and Ga) formed solid solutions with a wurtzite structure, while In showed complex layer stacking defects. For 3d magnetic cations (Mn, Fe, and Co), a broad solubility range in the hexagonal structure was noted for Mn, whereas Fe and Co more readily formed cubic structures, with solubilities similar to Mn in the sphalerite form. Despite structural differences, magnetic susceptibilities and spin freezing temperatures for Fe and Co were comparable. Group 14 elements showed varied behaviors: Sn was insoluble in ZnS, as attested by unchanged unit cell parameters and surface crystallite Sn, whereas Ge only formed in the cubic phase with a solubility limit of x ≈ 0.2. The study discusses these variations in solubility and structure in terms of oxidation states, ionic-covalent radius, and coordination preferences in sulfides.

Influence of carbon black surface characteristics on CB-NR interfacial interaction: Molecular simulation and experimental study

Carbon black (CB) is the most widely used reinforcing filler in rubber industry, but the effects of CB surface characteristics on interfacial interaction of CB-filled rubber composites are still not fully described. Combined the experimental and molecular simulation techniques, the aim of this study is to individually investigate the influence of various CB surface characteristics, such as surface area, surface crystallite size, roughness and surface energy, on CB-natural rubber (NR) interfacial interaction to obtain a deep interpretation on the properties of rubber composites. Experimental results showed that the specific surface area is the primary factor affecting overall CB-NR interaction, followed by filler network. Meanwhile, CB surface model with different roughness based on experimental parameters were constructed, and the simulation results revealed that CB-NR interfacial interaction mainly occurred at the interface 2–3 nm. The binding energy distribution on CB surface was analyzed, and rough region is weaker than crystal region and amorphous region. The strongest binding sites are located at the junction of rough region and amorphous region. The results in this study are expected to provide a theoretic guide for optimizing the CB characteristics and developing new rubber-grade CB.

Synthesis and fabrication of proto-type microstrip patch antenna by using microwave dielectric ceramic nanocomposite material for C-band application

The microwave dielectric properties of Zn(1-x)TixAl2O4 (ZTA) ceramic nanomaterials were investigated with a focus towards their use as wireless antennas. The ZTA nanoparticles were prepared using the sol-gel technique at 700 °C for one hour. The inclusion of titanium decreased the nanomaterials' crystallite size and surface shape, which influenced their dielectric permittivity (εr). Based on the tested material and microwave antenna theory, ZTA was used to fabricate wireless patch antennas, which were then examined using a PNA series network analyzer. The measured results reveal that the return loss and impedance bandwidths of the antenna were −44.83 dB simulated and −34.88 dB measured, and 240 MHz for simulated and 220 MHz for measured, respectively. At 5.1 GHz operating frequency, the Zn0.94Ti0.06Al2O4-based patch antenna demonstrated an exceptional combination of return loss (-34.88 dB), compact size (9.3× 6.3 mm2), and broad bandwidth (220 MHz) as well as VSWR<2. Ultimately, the fabricated antenna showcases a gain of 4.24 decibels and a directivity of 5.97 decibels.

Phosphate uptake is an essential process for rapid bone mineralization during early diagenesis – evidence from bone alteration experiments

Bones and teeth are often the only fossil remains of vertebrates that are preserved over geological time in sedimentary rocks. They render valuable archives for geochemical proxies which are commonly used for paleo-reconstructions. However, the fossilization mechanisms of bone are not yet well understood. Crucial processes are the transformation of bioapatite into and the replacement of collagen by thermodynamically more stable apatite phases, such as fluorapatite. In the present study, aqueous alteration experiments on cortical bone samples were performed under simulated early diagenetic conditions in order to investigate whether and how an external phosphate (PO4) source affects post mortem bone mineralization. Additionally, abiotic oxygen isotope exchange mechanisms between bioapatite and aqueous solutions were assessed by using either 18O-enriched water or PO4 as a tracer. The presence of an external sedimentary 18O-labeled PO4 source led to a rapid formation of new fluorapatite crystallites at the sample’s margin that was highly enriched in 18O. Meanwhile, in the interior of the samples carbonate-poor hydroxylapatite formed through a dissolution-precipitation process without incorporating significant amounts of the 18O tracer. These two processes appear to act independently from each other. In samples exposed to 18O-labeled aqueous solutions lacking a PO4 source, no newly grown apatite crystallites were found, however in the interior of these samples, nano-crystalline carbonate-poor or -free hydroxylapatite precipitated. A comparatively low but uniform 18O-enrichment was measured from the sample’s margin towards its interior, which is assumed to have resulted from the adsorption of H218O onto crystallite surface sites and collagen. Overall, our results suggest that a fast incorporation of 18O-doped PO4 from the sediment source accelerated bone mineralization and consequently changed the oxygen isotope composition of the PO4 group in the bone mineral phase more rapidly and to a greater extent than in a diagenetic setting lacking additional external PO4. Dissolved PO4 from the taphonomic setting thus seems to be an important factor fostering bone fossilization and preservation as well as oxygen isotope alteration.

Correlation between the micro-shot peening coverage and surface microstructural evolution and fluoride-induced corrosion behavior in Monel 400 alloy

This study examines the influence of micro-shot peening (MSP) on Monel 400 alloy, focusing on surface microstructural evolution and fluoride-induced corrosion behavior compared to its solution annealed (SAed) counterpart. MSP treatments were conducted at various surface coverages (100%, 200%, 500%, 1000%, 1500%, and 2000%). Characterization encompassed microhardness, surface roughness, grazing incidence x-ray diffraction (GI-XRD), field emission scanning electron microscopy (FE-SEM) with electron backscatter diffraction (EBSD), and transmission electron microscopy (TEM). With increasing the MSP coverage to 2000%, the surface crystallite size decreased from approximately ∼30 µm in the SAed sample to 60 nm. TEM analysis emphasized dislocation slip and formation of dislocation structures as the primary mechanisms for the grain refinement. However, the 2000% coverage exhibited microcrack formation, compromising its hydrofluoric (HF) corrosion resistance. Electrochemical tests revealed severe localized corrosion in all MSP-treated samples except the 1500% coverage, which exhibited a minimum passive current density of 0.2–1.0 µA/cm2. Inductively coupled plasma optical emission spectroscopy (ICP-OES) of immersion solutions showed lower copper and nickel ion concentrations (<150 ppm) in the 1500% MSP-treated sample, indicating its enhanced corrosion resistance. X-ray photoelectron spectroscopy (XPS) identified NiO, NiF2, CuO, CuF2, and Cu(OH)2 phases in SAed and 1500% MSPed samples, with a higher concentration of copper oxide (CuO) in the corrosion film of the 1500% MSP-treated sample, contributing to its superior corrosion resistance.

Crystallization kinetics and structural development of Bi2GeO5 glass-ceramics fabricated by the modified incorporation technique

This study focuses on the fabrication and crystallization kinetics of bismuth germanate (Bi2GeO5) crystals in glass ceramics. Bismuth germanate glass-ceramics were produced from a base glass containing 58.4 mol% Bi2O3, 23.4 mol% GeO2, and 18.2 mol% B2O3 using a modified incorporation technique. Differential thermal analysis was used to determine the crystallization temperature. The X-ray diffraction results showed a dominant peak corresponding to the pure Bi2GeO5 phase, which has an orthorhombic crystal structure. The local Avrami exponent (n(x)) and local crystallization activation energy (Ec(x)) were determined using a non-isothermal method with heating rates ranging from 5 to 20 °C/min. The results indicated that the crystal growth process of the glass-ceramics occurred in all three dimensions, with Avrami exponent values ranging from 1.79 to 2.5. The microstructure also revealed uniform crystallization across the surface and bulk diffusion of crystallites. The modified incorporation method successfully enhanced the crystallization of Bi2GeO5 glass-ceramics, resulting in the transition from one-dimensional needle-like crystals to the desired crystal dimensions.

Efficient biological activity of acridine synthesised by using efficient nano catalyst

A simple and efficient protocol for 9-(4-methoxyphenyl)-3,3,6,6-tetramethyl-3,4,6,7,9,10-hexa hydroacridine-1,8(2H,5H)-dione (MPTH) was synthesised by conventional method by using efficient nano catalyst. The crystallite sizes (L) and surface area (S) of TiO2 are 10.44 nm and 140.32 m2/g. MPTH displayed wide inhibitions on the KB cell appearance with IC50 values 25.06 μg. The IC50 values of the MPTH imply that methoxy substituted compound holds more inhibitory effect against the cancer cells.

Ring-ring equilibration (RRE) of cyclic poly(L-lactide)s by means of cyclic tin catalysts

With 2,2-dibutyl-2-stanna-1,3-dithiolane (DSTL) and 2-stanna-1,3-dioxa-4,5,6,7-dibenzoxepane (SnBiPh) as catalysts ring-expansion polymerizations (REP) were performed either in 2 M solution using three different solvents and two different temperatures or in bulk at 140 and 120 °C. A kinetically controlled rapid REP up to weight average molecular masses (Mẃs) above 300 000 was followed by a slower degradation of the molecular masses at 140 °C, but not at 120 °C Furthermore, a low molecular mass cyclic poly(L-lactide) (cPLA) with a Mn around 16 000 was prepared by polymerization in dilute solution and used as starting material for ring-ring equilibration at 140 °C in 2 M solutions. Again, a decrease of the molecular mass was detectable, suggesting that the equilibrium Mn is below 5 000. The degradation of the molecular masses via RRE was surprisingly more effective in solid cyclic PLA than in solution, and a specific transesterification mechanism involving loops on the surface of crystallites is proposed. This degradation favored the formation of extended-ring crystallites, which were detectable by a “saw-tooth pattern” in their MALDI mass spectra.

Improved ultraviolet photodetector performances using solution-processed nitrogen-doped carbon quantum dots/ZnO hybrid thin films

We fabricated the solution-processed photodetectors using the nitrogen-doped carbon quantum dots/zinc oxide (NCQDs/ZnO) hybrid films and characterized using ultraviolet (UV) spot-light of 365 nm at 1 mW/cm2. The NCQDs adsorbed onto the surface and/or grain boundaries of ZnO crystallites control ZnO particle size (by capping) in the NCQDs/ZnO hybrid thin films, resulting in the improved film quality and decreased the dark current in the devices. The NCQDs to ZnO [%(w/v)] ratio of 1.2 × 10−3 in the hybrid film UV photodetector exhibits the stable and reproducible photoresponses with the highest responsivity & external quantum efficiency (which are ∼3 times higher), and detectivity (∼7.5 times higher) than the pristine ZnO based photodetector, attributed to the effective transfer of photogenerated electrons from NCQDs to ZnO nanoparticles in the hybrid film. The solution-processed NCQDs/ZnO hybrid films will be very much useful to improve the UV photodetector performances for the cost-effective commercial applications.