Wongwiriyapan, Winadda

Preferred name

Alternative Name

Wongwiriyapan, W.

Main Affiliation

Integrated Innovative Technology

winadda.wo@kmitl.ac.th

Now showing 1 - 8 of 8

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Hybrid gas sensor based on platinum nanoparticles/poly(methyl methacrylate)-coated single-walled carbon nanotubes for dichloromethane detection with a high response magnitude
(2016-05-01)
Muangrat, Worawut
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Yordsri, Visittapong
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Maolanon, Rungroj
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Pratontep, Sirapat
;
Porntheeraphat, Supanit
A dichloromethane (DCM) sensor with a high response magnitude was successfully fabricated using the integration of single-walled carbon nanotubes (SWNTs), poly(methyl methacrylate) (PMMA) and platinum nanoparticles (Pt NPs). A pristine SWNT network was first formed by drop-casting onto printed circuit board (PCB) substrates. Next, PMMA was coated onto the pre-dropped SWNT network by spin coating using a PMMA-toluene solution, followed by the deposition of Pt NPs by electron-beam evaporation (hereafter referred to as Pt/PMMA/SWNT). The Pt/PMMA/SWNT enabled an approximately 69-fold improvement in DCM detection compared to pristine SWNT. The high response magnitude of the Pt/PMMA/SWNT was successfully achieved because of the incorporation of PMMA and Pt functions. Swelling of the PMMA matrix as a result of DCM adsorption leads to PMMA volume expansion, thereby increasing the SWNT-SWNT distance, which results in an increase in the resistance. Pt NPs promote the dissociation of DCM to CO, and consequently the CO oxidation on the Pt NPs catalyst and electron donation from Pt NPs to SWNTs, resulting in an increase in the resistance. Moreover, a linear relationship was obtained between the sensor response of the Pt/PMMA/SWNT and the concentration of DCM. These results suggest that the integration of SWNTs with PMMA and Pt NPs is a promising approach for improving DCM detection at room temperature.
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Effect of metal catalysts on synthesis of carbon nanomaterials by alcohol catalytic chemical vapor deposition
(2013-12-31)
Muangrat, Worawut
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Porntheeraphat, Supanit
;
Wongwiriyapan, Winadda
Carbon nanomaterials (CNMs) were synthesized by alcohol catalytic chemical vapor deposition (CVD) at atmospheric pressure using different metal catalysts (Ni, Co and Fe) at a growth temperature of 700°C. Ni and Fe acted as active catalysts for multi-walled carbon nanotubes (MWNTs) growth, while Co acted as an active catalyst for bamboo-like MWNTs and carbon nanofibers (CNFs) growth. The CNMs synthesized from Ni catalyst showed the highest crystallinity with a small amount of by-products. These results imply that metal catalyst is a key parameter to the structure, morphology and crystallinity of CNMs. The different effects of metal catalysts on the growth of CNMs can be explained in terms of the difference in the change in Gibbs free energy of metal carbide formation.
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Piezoelectric-Induced Triboelectric Hybrid Nanogenerators Based on the ZnO Nanowire Layer Decorated on the Au/polydimethylsiloxane-Al Structure for Enhanced Triboelectric Performance
(2018-02-21)
Jirayupat, Chaiyanut
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Wongwiriyapan, Winadda
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Kasamechonchung, Panita
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Wutikhun, Tuksadon
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Tantisantisom, Kittipong
Here, we demonstrate a novel device structure design to enhance the electrical conversion output of a triboelectric device through the piezoelectric effect called as the piezo-induced triboelectric (PIT) device. By utilizing the piezopotential of ZnO nanowires embedded into the polydimethylsiloxane (PDMS) layer attached on the top electrode of the conventional triboelectric device (Au/PDMS-Al), the PIT device exhibits an output power density of 50 μW/cm<sup>2</sup>, which is larger than that of the conventional triboelectric device by up to 100 folds under the external applied force of 8.5 N. We found that the effect of the external piezopotential on the top Au electrode of the triboelectric device not only enhances the electron transfer from the Al electrode to PDMS but also boosts the internal built-in potential of the triboelectric device through an external electric field of the piezoelectric layer. Furthermore, 100 light-emitting diodes (LEDs) could be lighted up via the PIT device, whereas the conventional device could illuminate less than 20 LED bulbs. Thus, our results highlight that the enhancement of the triboelectric output can be achieved by using a PIT device structure, which enables us to develop hybrid nanogenerators for various self-power electronics such as wearable and mobile 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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Polymer-coated single-walled carbon nanotubes for ethanol and dichloromethane discrimination
(2013-10-29)
Muangrat, Worawut
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Maolanon, Rungroj
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Pratontep, Sirapat
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Porntheeraphat, Supanit
;
Wongwiriyapan, Winadda
Sensor response and pattern recognition of polymer-coated single-walled carbon nanotubes (SWNTs) were investigated. Printed circuit board (PCB) with Cu/Au interdigitated electrode was used as sensor platform. SWNTs network was firstly formed on PCB by drop-casting. For polymer-coated SWNTs preparation, poly(methyl methacrylate) (PMMA) and thiophene were employed as polymers to coat on SWNTs by spin coating; PMMA/SWNTs and thiophene/SWNTs. Raman spectra showed no obvious structure changes of SWNTs after polymer coating. Next, gas sensing test was conducted. Pristine SWNTs, PMMA/SWNTs and thiophene/SWNTs were exposed to vapors of ethanol and dichloromethane at room temperature. From normalized sensor response results, it was found that pristine SWNTs and PMMA/SWNTs showed the highest response to ethanol and dichloromethane vapors, respectively. In order to discriminate vapors between ethanol and dichloromethane, pattern recognition technique was utilized. Principal component analysis (PCA) results showed that pattern recognition of ethanol and dichloromethane vapors can be discriminated by using pristine SWNTs and polymer-coated SWNTs sensors. © (2013) Trans Tech Publications, Switzerland.
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Poly(methyl methacrylate) and thiophene-coated single-walled carbon nanotubes for volatile organic compound discrimination
(2016-02-01)
Muangrat, Worawut
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Chodjarusawad, Thanawee
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Maolanon, Rungroj
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Pratontep, Sirapat
;
Porntheeraphat, Supanit
Poly(methyl methacrylate) (PMMA) and thiophene-coated single-walled carbon nanotubes (SWNTs) were fabricated for use in volatile organic compound (VOC) detection. Pristine SWNTs were separately coated with PMMA (PMMA/SWNTs) and thiophene (thiophene/SWNTs) by spincoating. Pristine SWNTs showed the highest response to methanol, while PMMA/SWNTs enabled 5.4-fold improved dichloromethane detection and thiophene/SWNTs enabled 1.4-fold improved acetone detection compared with pristine SWNTs. The sensor response of PMMA/SWNTs to dichloromethane and that of thiophene/SWNTs to acetone can be attributed to the Hildebrand solubility parameter (HSP). The more similar the HSP, the higher the sensor response. The sensor response of pristine SWNTs to methanol is related to the diffusion coefficient and molecular size. The relationships between the vapor concentration and sensor response of PMMA/SWNTs to dichloromethane and thiophene/SWNTs to acetone are based on Henry's adsorption isotherm, while that of pristine SWNTs to methanol is based on the Henry-clustering model. Principal component analysis (PCA) results show that dichloromethane, acetone, and methanol were successfully discriminated.
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Texture orientation of silver thin films grown via gas-timing radio frequency magnetron sputtering and their SERS activity
(2016-01-01)
Ukahapunyakul, Pongbordin
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Gridsadanurak, Nurak
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Sapcharoenkun, Chaweewan
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Treetong, Alongkot
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Kasamechonchung, Panita
Here we demonstrate a special technique to control a texture orientation of silver (Ag) thin films using gas-timing (GT) rf magnetron sputtering. By utilizing a GT technique, a dense structure and a high ratio of (111)/(200) of Ag films could be obtained without applying additional energy sources. We found that the GT technique not only provides the ability to adjust the number of sputter species from the target, but also generates the self-energy assisted deposition which related to the atomic peening effect. Furthermore, we found that a high (111)/(200) ratio of Ag films strongly affects the SERS activity of the Ag films due to a hot spot effect. Our results highlight that the texture engineering of metal thin films could be accomplished by using a GT technique.
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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.

Wongwiriyapan, Winadda

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