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Tailoring ZnO Nanostructures through Precursor Concentration and Hydrothermal Duration: A Pathway to Efficient Solar Water Splitting
(2026-11-10)
Borklom, Phanlapa
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Khemasiri, Narathon
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Jessadaluk, Sukittaya
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Rattanawarinchai, Prapakorn
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Kayunkid, Navaphun
This work investigated the formation of ZnO nanostructures on ITO substrates prepared by self-seeding hydrothermal synthesis for photoelectrochemical ( PEC) water splitting applications. The hydrothermal parameters, precursor concentration and hydrothermal time, were varied to explore their influences on ZnO crystallinity, morphology, and PEC performance. The combinations of X-ray diffraction and field emission scanning electron microscopy revealed highly oriented ZnO nanostructures with diverse morphologies, including small granules, nanorods, dense films, and hexagonal platelets. Topographic profiling of the morphological parameters revealed complex relationships between synthesis conditions and nanostructure characteristics, highlighting the importance of considering aggregation phenomena in substrate-based growth. This aggregation led to deviations from conventional crystal growth theory predictions, particularly for grain density and diameter evolution. PEC performance evaluation identified ZnO nanorods as the optimal morphology, exhibiting a photocurrent density of 0.182 mA/cm² at 0 V vs. Ag/AgCl. Further enhancement was achieved by decorating ZnO nanorods with CdS nanoparticles, resulting in a six-fold increase in photocurrent density (1.2 mA/cm²). This improvement is attributed to expanded light absorption and improved charge separation at the CdS/ ZnO interface. Our findings demonstrate the potential of rationally designed ZnO-based nanostructures in the advancement of solar-driven water splitting technologies and provide valuable insights for optimizing PEC systems through precise control of hydrothermal synthesis parameters, consideration of substrate-induced aggregation, and strategies for photoelectrochemical (PEC) water splitting applications.
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Growth window and metal-insulator transition behavior of VO2 thin films deposited by pulsed laser deposition for thermal switch applications
(2026-05-01)
Jessadaluk, Sukittaya
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Rahong, Sakon
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Kayunkid, Navaphun
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Khemasiri, Narathon
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Rangkasikorn, Adirek
Vanadium dioxide (VO<inf>2</inf>) is a strongly correlated transition metal oxide that exhibits a sharp and reversible metal-insulator transition (MIT) near room temperature, making it a promising material for thermal switching and adaptive electronic applications. In this study, VO<inf>2</inf> thin films were deposited on single-crystalline Si, thermally grown SiO<inf>2</inf>, and fused quartz substrates by pulsed laser deposition, and the influence of substrate temperature and oxygen partial pressure on phase formation, structural properties, and MIT behavior was systematically investigated. By optimizing deposition conditions within a narrow oxygen pressure window, phase-pure monoclinic VO<inf>2</inf>(M) thin films with high crystalline quality were achieved while suppressing the formation of over-oxidized vanadium oxide phases. Structural and chemical analyses using X-ray diffraction, Raman spectroscopy, and X-ray photoelectron spectroscopy confirmed the stabilization of the V4+ oxidation state and uniform film stoichiometry. Temperature-dependent electrical measurements revealed a pronounced and reproducible MIT characterized by an abrupt change in resistance and a clear thermal hysteresis. In-situ temperature-dependent X-ray diffraction further demonstrated a direct correlation between the monoclinic-rutile structural transformation and the electronic transition. Importantly, the MIT behavior was consistently observed across all investigated substrates, indicating robust film growth and substrate tolerance. These results provide insight into the structure-property relationships governing VO<inf>2</inf> thin films and highlight their potential for integration into thermal switch and thermally adaptive device architectures.
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Oil palm leaf-derived nanoporous carbon via hydrothermal carbonization combined with NaOH microwave activation for tetracycline adsorption
(2025-11-01)
Chanpee, Sirayu
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Apinyakul, Naruemon
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Kaewtrakulchai, Napat
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Khemasiri, Narathon
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Eiad-ua, Apiluck
Generally, the increase in pharmaceutical industrial activities has led to a corresponding rise in water resource contamination. Efforts have been dedicated to addressing the urgent challenge of waste biomass disposal by developing recycling methods capable of producing bio-adsorbents. Adsorption is a promising approach for removing tetracycline contaminants, owing to its simplicity, stability, and cost-effectiveness. In this study, a low-cost activated biochar was successfully developed using oil palm leaf (OPL) via hydrothermal carbonization (HTC) combined microwave-assisted pyrolysis system (MAPS) using sodium hydroxide (NaOH). The HTC and MAPS processes enhanced high mass yield, porosity, energy efficiency, and reduced reaction time. NaOH treatment improved the porosity of the activated biochar derived from OPL, resulting primarily in a mesoporous structure. However, NaOH treatment via the MAPS process increased surface area and porosity. Among the samples tested, OPLC-NaOH-1:1 exhibited the largest surface area and highest porosity, making it the chosen candidate for further TC adsorption tests. The adsorption experiments revealed that the Langmuir isotherm model and the pseudo-second-order kinetic model accurately matched the experimental data, suggesting a mono-layered adsorption mechanism due to micropores and chemisorption interactions. Additionally, thermodynamic analysis indicated an endothermic and spontaneous reaction during the adsorption process. The adsorption of nanoporous carbon for TC was primarily regulated by pore filling, hydrogen bonding, electrostatic effects, and π-π interactions also playing a significant role. Overall, this study highlights the potential of utilizing OPL waste as a sustainable material for producing nanoporous carbon and underscores the effectiveness of nanoporous carbon for adsorbing antibiotics.
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Rational concept for fully designing metal-oxynitride films through reactive gas-timing magnetron sputtering: A case study on zinc oxynitride film
(2025-08-10)
Khemasiri, Narathon
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Chananonnawathorn, Chanunthorn
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Horprathum, Mati
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Pornthreeraphat, Supanit
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Saekow, Bunpot
Amorphous metal-oxynitride films—particularly zinc oxynitride (ZnON)—are emerging as promising materials for next-generation high-speed switching electronics, due to the absence of a potential barrier above the conduction band, unlike metal-doped ZnO. However, conventional reactive magnetron sputtering often face challenges in precisely controlling in an anion ratio, N/(N + O), because of the different reactivities of nitrogen and oxygen gases. In this work, we present a strategy to precisely control both the crystal structure and N/(N + O) ratio in ZnON films using a reactive gas-timing technique. By adjusting the oxygen gas-timing sequence (t<inf>O₂</inf>), we selectively induce different crystalline phases, which are closely related to the nitridation and oxidation of the sputtered Zn atom/cluster. This technique facilitates effective N incorporation into ZnO, enabling a broad range of N/(N + O) ratios from 0.048 to 0.964 and optical band gap variations from 1.49 eV to 3.22 eV. At an optimal t<inf>O₂</inf>, an amorphous phase is formed, attributed to a balanced nitridation and oxidation rate of the sputtered Zn atom/cluster that suppresses crystallization. The resultant amorphous ZnON film exhibits a high carrier mobility of 84.81 cm²/Vs, which is 1.16-fold and 35.89-fold greater than those of the cubic and hexagonal ZnON films, respectively. Our findings highlight the effectiveness of the reactive gas-timing technique as a powerful tool for the rational design of metal-oxynitride films, paving the way for their application in advanced electronic devices.
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Laser-induced graphene electrochemical immunosensors for rapid and sensitive serological detection: A case study on dengue detection platform
(2025-06-01)
Inlumphan, Supawee
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Wongwiriyapan, Winadda
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Khemasiri, Narathon
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Rattanawarinchai, Prapakorn
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Leepheng, Piyawan
Here, we present a diagnostic on a chip platform based on laser-induced graphene (LIG) electrochemical immunosensors for serological detection. The electrochemical immunosensors are fabricated through CO<inf>2</inf> laser induction on polyimide (PI) sheets. Optimal electrochemical activity of LIG electrodes is obtained under optimized conditions of laser fluence. To verify the application, the serological detection platform was demonstrated. After functionalization with dengue virus (DENV) antigen, the LIG electrochemical immunosensors are able to sense the presence of mouse anti-flavivirus monoclonal (4G2) antibody in a wide linear working range of 25–20,000 ng/ml with the limit of detection (LOD) of 17.41 ng/ml. A specific recognition with 4G2 antibodies against with media protein and isotype is confirmed. Furthermore, the reliability of LIG electrochemical immunosensors compared to conventional enzyme-linked immunosorbent assay (ELISA) is verified through the NS1 antibodies identification in human blood serum clinical samples at room temperature. Our results highlight that the LIG-based electrode is a promising platform for electrochemical immunosensors, aimed at developing reliable and practical diagnostic tools for serological detection. These tools enable early diagnosis of infectious diseases, as well as non-invasive and rapid screening.
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Selective formations of antimony-dopant for highly sensitive nitrogen dioxide responsive behavior of tin oxide-based chemiresistive sensor
(2025-02-15)
Rattanawarinchai, Prapakorn
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Khemasiri, Narathon
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Rahong, Sakon
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Rangkasikorn, Adirek
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Kayunkid, Navaphun
Here, selective formation of antimony (Sb) dopant species responsible for highly sensitive gas sensors based on tin oxide (SnO<inf>2</inf>) film grown via pulsed laser deposition is presented. By elevating a forming energy through controlling substrate temperature, not only crystallinity of Sb-SnO<inf>2</inf> (ATO) is notably enhanced but the Sb5 + also predominantly replace at Sn4+ site rather than Sb3+ counterpart. Such Sb-species selection plays a crucial role on the density of oxygen vacancy and free electron enabling to rationally design conductive behaviour of ATO film from insulative to degenerated semiconductor. As a practical example, detection of nitrogen dioxide (NO<inf>2</inf>) gas is selected as an application model. We found a narrow window for high NO<inf>2</inf> sensing performance of ATO film which strongly corresponds with the amount of carrier density. At certain window, ATO film exhibits high NO<inf>2</inf> response of 24.65 (10 ppm) and low limit of detection of 0.5 ppm, which is 5-fold higher and 10-fold lower than that of undoped-SnO<inf>2</inf>, respectively. Our finding demonstrates a facile approach to design over the chemical state, defect, and conductivity of the active sensing layer, allowing us to achieve an excellent sensing performance of functional materials conjugated to a nano-electronic platform.
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Low resistance bisphenol-A based polybenzoxazine derived laser-induced graphene (LIG) and its microsupercapacitor application
(2024-11-01)
Luengrojanakul, Panuwat
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Klamchuen, Annop
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Khemasiri, Narathon
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Chotsuwan, Chuleekorn
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Charoensuk, Krittapas
Herein, we demonstrate the use of conventional BA-a based polybenzoxazine as a laser-induced graphene (LIG) forming precursor. The effects of laser power and the engraving speed on formation and properties of LIG are explored. By optimizing the laser fluency related to laser power along with engraving speed, poly(BA-a) derived LIG with high graphitization degree and low sheet resistance (R<inf>s</inf>) of ∼ 2–10 Ω/sq can be acquired. The morphologies and surface area of LIGs in such low R<inf>s</inf> region are then validated through SEM and BET, respectively. The resulting poly(BA-a) derived LIG exhibits a high amount of macropores in the structure with marginal differences in the specific surface area being 27–88 m2/g. In addition, electrochemical performances of the two-electrode based microsupercapacitor (LIG-MSC) of the selected samples in low R<inf>s</inf> region with different specific surface area are evaluated. The LIG-MSC shows a specific capacitance of 1.39 mF/cm2 (0.04 mA/cm2), and good cycling stability of 10,000 cycles with capacitance retention of 92% (0.2 mA/cm2). Our results highlight that poly(BA-a) derived LIG is promising for high performance LIG applications.
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Synthesis of nanoporous carbon from brewer waste by hydrothermal carbonization assisted chemical activation for carbamazepine adsorption
(2024-06-01)
Apinyakul, Naruemon
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Chanpee, Sirayu
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Kaewtrakulchai, Napat
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Khemasiri, Narathon
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Eiad-ua, Apiluck
Nanoporous carbon (NPC) has gained significant attention in wastewater treatment due to its effectiveness. The adsorption process, known for its simplicity, stability, and cost-effectiveness, is widely recognized as an efficient method for removing carbamazepine (CBZ) residues accumulate in the environment. However, the application of NPC is often hindered by challenges in the regeneration process after use, as well as issues related to large surface area, pore size, and functional groups. Fortunately, the samples in this study not only maintained their adsorption efficiency but also demonstrated the ability to be regenerated multiple times. Herein brewery waste was subjected to hydrothermal treatment at 200 °C for 1 h and followed by KOH and NaCl activation with different KOH:NaCl (w/w) ratios of 5:0, 4:1, 3:2, 1:1, 2:3, 1:4, and 0:5 to optimize the properties of malt husk derived nanoporous carbon (NPC). The optimal condition KOH:NaCl ratio of 1:1 had a maximum specific surface area of 906 m2/g with a total pore volume of 0.252 cm3/g. According to the adsorption test, the CBZ adsorption isotherm was well-fitted to the Langmuir model (R2 = 0.976) kinetic data were consistent with the pseudo-second-order model (R2 = 0.995). This suggests that the adsorption mechanism involves monolayer adsorption and chemisorption interaction. The Gibbs free energy and enthalpy of CBZ adsorption by NPC were found to be spontaneous and endothermic. The regeneration test revealed a 95.35% decrease in the adsorption capacity of NPC after 5 repeated cycles. Consequently, the study suggests a potential application of nanoporous carbon from MH as an alternative adsorbent for removing carbamazepine in wastewater.
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Reusability, Long-Life Storage and Highly Sensitive Zirconium Nitride (ZrN) Surface-Enhanced Raman Spectroscopy (SERS) Substrate Fabricated by Reactive Gas-Timing Rf Magnetron Sputtering
(2023-12-22)
Sucheewa, Nguentra
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Wongwiriyapan, Winadda
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Rattanawarinchai, Prapakorn
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Wuttikhun, Tuksadon
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Sinthiptharakoon, Kittiphat
Transition metal nitrides (TMN) are promising material alternative to replace noble metals in the field of plasmonic applications, especially surface-enhanced Raman spectroscopy (SERS). Here we demonstrate a practical surface enhanced Raman spectroscopy (SERS) substrate using zirconium nitride (ZrN) thin films grown by reactive gas-timing (RGT) rf magnetron sputtering. The tailored properties of ZrN thin film exploited for SERS activity could be achieved to obtain a highly sensitive ZrN thin film SERS substrate with the enhancement factor (EF) of 1.24 × 106 and 4.8 %RSD at 1626 cm-1 toward methylene blue (MB) analyte which are comparable to the optimized Au sputtered thin films (EF=1.18 × 106 and with 5.1%RSD). We find that the spatial plasmonic hotspots on the surface of ZrN SERS substrate controlled by the turn-on timing of Ar:N2 sputtered gas sequence, leading to the discrete conductive surface profile, strongly relates to non-stoichiometric composition and the degree of (200)-oriented texture at the surface of ZrN thin film. Furthermore, ZrN thin film SERS substrates exhibit an excellent recyclability more than 30 cycles with simple cleaning process and a storage time longer than 6 months. The detection and reusability of ZrN SERS substrate on the low concentration of trinitrotoluene (TNT) for homeland security are also performed.
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Influence of Antimony Species on Electrical Properties of Sb-Doped Zinc Oxide Thin Films Prepared by Pulsed Laser Deposition
(2023-06-01)
Jessadaluk, Sukittaya
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Khemasiri, Narathon
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Kayunkid, Navaphun
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Rangkasikorn, Adirek
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Wirunchit, Supamas
This study systematically investigates the influence of antimony (Sb) species on the electrical properties of Sb-doped zinc oxide (SZO) thin films prepared by pulsed laser deposition in an oxygen-rich environment. The Sb species-related defects were controlled through a qualitative change in energy per atom by increasing the Sb content in the Sb<inf>2</inf>O<inf>3</inf>:ZnO-ablating target. By increasing the content of Sb<inf>2</inf>O<inf>3</inf> (wt.%) in the target, Sb3+ became the dominant Sb ablation species in the plasma plume. Consequently, n-type conductivity was converted to p-type conductivity in the SZO thin films prepared using the ablating target containing 2 wt.% Sb<inf>2</inf>O<inf>3</inf>. The substituted Sb species in the Zn site (Sb<inf>Zn</inf>3+ and Sb<inf>Zn</inf>+) were responsible for forming n-type conductivity at low-level Sb doping. On the other hand, the Sb–Zn complex defects (Sb<inf>Zn</inf>–2V<inf>Zn</inf>) contributed to the formation of p-type conductivity at high-level doping. The increase in Sb<inf>2</inf>O<inf>3</inf> content in the ablating target, leading to a qualitative change in energy per Sb ion, offers a new pathway to achieve high-performing optoelectronics using ZnO-based p–n junctions.

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