Maluangnont, Tosapol

Preferred name

Alternative Name

Maluangnont, T.

Main Affiliation

Integrated Innovative Technology

tosapol.ma@kmitl.ac.th

Now showing 1 - 10 of 62

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Titanate Nanosheets/Cellulose Composite Showing Improved Crystallinity and Decreased Water Wettability by Gamma-Irradiation
(2025-11-25)
Tariwong, Yaowaluk
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Pulphol, Phieraya
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Sangtawesin, Tanagorn
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Seriwattanachai, Chaowaphat
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Kanjanaboos, Pongsakorn
While molecularly thin nanosheets have been increasingly studied as functional coatings, their use as a hydrophobic and γ-irradiation-tolerant component in biologically derived matrices is to be demonstrated. Herein, simple dip-coating was employed to fabricate titanate nanosheets/cellulose composites, which were subjected to γ-irradiation up to 50 kGy. Their surface chemistry was evaluated by water contact angle (WCA) measurements and X-ray photoelectron spectroscopy (XPS). Upon irradiation, the WCA of all samples nonmonotonically increased in three stages from ∼29 to 50° (noncoated) and ∼46 to 80° (composite, optimized at ∼1.2 wt %Ti loading, or 0.2 mg·cm–2). The titanium content and the 4+ valence did not change with the dose, suggesting the radiolytic stability. The dual surface modification occurs while cellulose fiber morphology and nanoscale mechanical properties are preserved. The increased WCA at the cellulose-part is explained by the γ-irradiation-induced crystallization according to the increased crystallinity index and improved thermal stability. At the other component, nanosheet coating results in increased surface roughness and diminished water–surface interactions. The latter is deduced from DSC measurements of water evaporation from pristine and 50 kGy-irradiated Cs<inf>0.7</inf>Ti<inf>1.825</inf>O<inf>4</inf>layered crystal-a nanosheet precursor. Our work suggests further exploration of nanosheets with diverse structures and compositions as coatings or fillers, which could find applications in γ-irradiation-sterilized barrier films.
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Tailoring charge affinity, dielectric property, and band gap of bacterial cellulose paper by multifunctional Ti2NbO7 nanosheets for improving triboelectric nanogenerator performance
(2023-02-01)
Sriphan, Saichon
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Pharino, Utchawadee
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Charoonsuk, Thitirat
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Pulphol, Phieraya
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Pakawanit, Phakkhananan
Transparent, flexible, and high-performance triboelectric nanogenerator (TENG) from nature-derived materials are required for sustainable society development. However, low triboelectricity from natural material is generally observed. Tunable electronic band diagram (EBD) through facile manipulation is one of the efficient methods to promote the TENG output, requiring fundamental, in depth understanding. Herein, we employed the high quality, single crystal-like Ti<inf>2</inf>NbO<inf>7</inf> nanosheets (NSs) with dual dielectric and semiconducting properties as filler for bacterial cellulose (BC)-based TENG. Several techniques including X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), ultraviolet—visible (UV—vis) absorption, energy dispersive X-ray spectroscopy (EDS), and synchrotron radiation X-ray tomographic microscopy (SRXTM) were applied to characterize the long-range structure, microstructure, optical properties, elemental composition, and three-dimensional (3D) distribution of components in the composites. The semi-transparent and flexible 5 vol.% Ti<inf>2</inf>NbO<inf>7</inf> NSs/BC preserved the integrity of cellulose, contained well-dispersed nanosheets, reduced optical band gap (4.20 vs. 5.75 eV for BC), and increased surface roughness. The dielectric permittivity and conductivity increased with nanosheets content. Adding negatively-charged Ti<inf>2</inf>NbO<inf>7</inf> NSs could regulate the charge affinity of BC composite via shifting of Fermi energy over that of Al. It is found that adding 5 vol.% NSs into the BC film improved electrical outputs (~ 36 V and ~ 8.8 µA), which are 2–4 times higher than that of pure BC, even when paired with Al which lies adjacent in triboelectric series. Our work demonstrated the method to enhance BC-based TENG performance through EBD regulation using multifunctional Ti<inf>2</inf>NbO<inf>7</inf> NSs. [Figure not available: see fulltext.]
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Electrical and dielectric properties of barium titanate–polydimethylsiloxane nanocomposite with 0-3 connectivity modified with carbon nanotube (CNT)
(2019-01-02)
Nawanil, Chanisa
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Makcharoen, Worawut
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Khaosa-Ard, Krittanat
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Maluangnont, Tosapol
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Vittayakorn, Wanwilai
This study explored the preparation and electrical properties of 0–3 barium titanate/polydimethylsiloxane nanocomposites by dispersing barium titanate nanoparticles (BaTiO<inf>3</inf>; BT) into the polydimethylsiloxane (PDMS) matrix phase. The effect of barium titanate nanoparticles on electrical properties has been investigated systematically, and the relative permittivity of nanocomposites was found to increase significantly with increasing barium titanate content. Different theoretical models were used to predict the dielectric constant of these composites and compare their experimental value with the theoretical value in order to find an appropriate equation. The result indicated that the dielectric properties of composites are influenced not only by relative permittivity of the components but also dependence on interactions between ceramics and polymers. Furthermore, the preparation and dielectric properties of BT/PDMS nanocomposites modified with carbon nanotube (CNT) were also studied. The dielectric results demonstrate that adding CNT can enhance the relative permittivity of the BT/PDMS composite via improvement of dispersion and distribution of the BT nanoparticles in the PDMS matrix phase. Moreover, the electrical outputs from the BT/PDMS/CNT nanocomposites generator were measured under periodic knocking. The nanocomposites innovatively expand the feasibility of self-powered energy systems for smart sensor and energy harvesting applications.
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Highly Flexible Tribovoltaic Nanogenerator Based-on P-N Junction Interface: Comparative Study on Output Dependency Dominated by Photovoltaic Effect in Freestanding-Mode
(2023-10-18)
Sriphan, Saichon
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Worathat, Supakarn
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Pharino, Utchawadee
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Chanlek, Narong
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Pakawanit, Phakkhananan
The emergence of tribovoltaic nanogenerators (TVNGs) paves the way for developing a new kind of semiconductor-based energy harvester that overcomes the restriction of low output current in a conventional approach. The traditional TVNG generally depends on the frictional pair between two rigid semiconductors (or metal-semiconductor), limiting the practicability of flexible and portable electronics. Recent developments require the fundamental understanding of charge generation in diverse operating modes and structures. Here, a flexible TVNG based on the p-Cu<inf>2</inf>O/n-g-C<inf>3</inf>N<inf>4</inf> interface is presented. Operating in a freestanding mode, the proposed TVNG can generate a stable signal in any optical conditions including UV illumination, dark, and ambient. Under UV illumination, the electrical outputs of the TVNG reach 0.43 V and 2.1 µA cm−2, which are significantly larger than those obtained from dark and ambient conditions. The results demonstrate the coupling effect of three phenomena: tribovoltaic, photovoltaic, and triboelectric effects, and the unique mechanism to the observed signal is proposed. Additionally, the TVNG shows the practical feasibility of energy harvesting with capacitor charging and charge-boosting circuits. This study showcases the unique concept with potential for developing a novel flexible nanogenerator in many aspects, including material, structure, and fundamental mechanism.
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Strain engineering and thermal conductivity of a penta-BCN monolayer: A computational study
(2021-09-01)
Dabsamut, Klichchupong
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Thanasarnsurapong, Thanasee
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Maluangnont, Tosapol
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T-Thienprasert, Jiraroj
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Jungthawan, Sirichok
Two-dimensional (2D) pentagonal nanostructures have been caught research attention down to their electronic, optical, mechanical and thermal transport properties. Among them, the newly proposed ternary penta-BCN monolayer shows a great potential for piezoelectric materials according to intrinsic piezoelectricity and spontaneous polarization. Nevertheless, the effect of strain toward these properties of the penta-BCN has not been elucidated. In this study, using density-functional theory with the Perdew-Burke-Ernzerhof (PBE) functional, we have investigated the impact of a uniform biaxial strain on the electronic structure and the thermal conductivity of the semiconducting penta-BCN single sheet. The strain-free penta-BCN monolayer is mechanically and dynamically stable with an indirect band gap of 1.70 eV. The sheet is rather soft as judged from the low in-plane Young's moduli. The pentagonal structure is preserved up to the yielding point of 18.4%, beyond this point the irreversible transition into the dynamically unstable, honeycomb-like system is observed. In contrast, the penta-BCN has dynamically instability under the compressive strain as small as -4%. The PBE band gap of the penta-BCN monolayer could be tuned within a range of 1.36-1.70 eV, falling into the infrared spectrum. The calculated lattice thermal conductivity of penta-BCN is around 97 W m-1 K-1 at temperature of 300 K, and decreases with increasing temperature.
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AC Electrical Properties of a NiFe-Layered Double Hydroxide with an Exceptionally Low Charge Density
(2025-05-08)
Maluangnont, Tosapol
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Sriphan, Saichon
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Chaithaweep, Kanokwan
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Vittayakorn, Naratip
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Wijitwongwan, Rattanawadee Ploy
Single-phase NiFe-layered double hydroxides (LDHs) with low and high charge densities [CD, 0.85 vs 3.23 nm-2; FeIII/(NiII + FeIII) = 0.05 and 0.25] were successfully prepared via urea-assisted coprecipitation in aqueous glycerol under hydrothermal conditions. The low-CD NiFe-LDH showed decreased apparent activation energies of water evaporation and of glycerol thermal decomposition, suggesting diminished intercalate/layer interactions relative to the high-CD one. The alternating current properties of the two samples were investigated on frequency and temperature domains by several formalisms that highlight distinct electrical components. We found that the low-CD NiFe-LDH exhibited smaller static dielectric permittivity and slower relaxation time, and it was less conducting than the high-CD analog. Complex plane analyses revealed the temperature dependence of resistance and capacitance at grain and grain boundary, varying by 7-10 orders of magnitude due to water loss and glycerol loss (∼9.5 and 11.3 wt %, respectively). Our work provides insights into intercalate dynamics in a low charge density LDH, which is difficult to obtain so far, from ambient to elevated temperatures (RT-250 °C) prior to decarbonation and layer collapse.
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AC Conductivity and dielectric properties of lepidocrocite-type alkali titanate tunable by interlayer cation and intralayer metal
(2020-11-02)
Charoonsuk, Thitirat
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Sriphan, Saichon
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Pulphol, Phieraya
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Vittayakorn, Wanwilai
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Vittayakorn, Naratip
The lepidocrocite-type layered alkali titanate AxMyTi2-yO4 has diverse chemical compositions with variation in charge per formula unit x, the interlayer cation A+, and the intralayer metal M. Despite this multivariable nature, the composition dependence of physical properties is not well explored. We report herein the AC conductivity and the complementary dielectric properties of Cs0.7M0.35Ti1.65O4, K0.8M0.4Ti1.6O4 (M = Zn, Ni), and the mixed-interlayer ion Cs0.6K0.1Zn0.35Ti1.65O4. For Cs0.7Zn0.35Ti1.65O4, the total AC conductivity is ~7 × 10-8 to 2 × 10-6 S·cm-1 at 200-350 °C, associating with an activation energy Ea ∼865 meV. Meanwhile, the conductivity of K0.8Zn0.4Ti1.6O4 is higher by 1 order of magnitude at much lower temperature (25-150 °C) and a smaller Ea ∼250 meV. This difference originates from the compositional robustness of the cesium-containing samples, contrasting with the sintering-induced changes in the potassium analogues. For the latter, the loss of the interlayer K+ ion results in (i) generation of carriers due to charge compensation, (ii) reduction of sheet charge density and weakening of electrostatic attraction, and (iii) widening of the interlayer distance, all contributing to a lower Ea in K0.8M0.4Ti1.6O4. The angular frequency dependence of conductivity, dielectric permittivity (up to a colossal value of 109), and dielectric loss follows the universal power law. Our work demonstrates the potential of simple compositional variation for electrical properties tuning, prompting a more in-depth investigation covering a wider range of possible candidates of x, A+, and M in lepidocrocite titanate.
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Towards the preparation of organic ferroelectric composites: fabrication of a gamma-glycine-bacterial cellulose composite via cold sintering process
(2023-07-01)
Noisak, Jitrawan
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Charoonsuk, Thitirat
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Pongampai, Satana
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Pinpru, Nattapong
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Pakawanit, Phakkhananan
The cold sintering process (CSP) has emerged as a revolutionary technique for low-temperature processing of ceramics and composites, enabling high-density fabrication at low temperatures. In this study, we demonstrated the implementation of CSP in fabricating the γ-glycine (γ-G)-bacterial cellulose (BC) composite and evaluated the effect of sintering temperature and holding time on the microstructure and electrical properties. Our findings revealed that an increase in sintering temperature and holding time leads to grain growth, as the transient solvent (water) facilitates the closely-packed microstructure. Moreover, the addition of BC as a filler into the γ-G matrix leads to a composite with a 10% increase in hardness when BC was uniformly distributed in γ-G. The composite with a relative density of 97% was successfully obtained at 120 °C/24 h, preserving the γ polymorph of glycine without the unwanted transformation commonly observed with traditional sintering. We also reported the dielectric and ferroelectric properties of the γ-G-BC composite, exhibiting a remanent polarization of 0.004 μC/cm2 and a coercive field of 1.201 kV/cm. Our findings suggest that CSP is a promising approach for low-temperature processing and fabrication of ceramics, especially when incorporating structurally sensitive filler such as organic ferroelectric, to achieve high-performance composites.
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An architected silk fibroin-lignin multilayer with deep-level trapping states for high-output triboelectric nanogenerators
(2026-03-01)
Suktep, Natdanai
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Sae-tang, Chanachot
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Ukasi, Sirinya
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Pakawanit, Phakkhananan
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Supansomboon, Supitcha
Biopolymer-based triboelectric nanogenerators (B-TENGs) are promising power sources for sustainable and flexible electronics, but their performance is often limited by severe charge recombination at the triboelectric interface. To overcome this critical bottleneck, we report an architected multilayer B-TENG featuring a silk fibroin (SF)/MgAl LDH composite as the charge-generating layer and, to our knowledge, for the first time, a lignin-functionalized SF film as a dedicated charge-trapping layer. The strategic incorporation of lignin, an abundant and sustainable biopolymer, introduces deep-level electronic trapping states originating from its abundant aromatic moieties. That effectively suppresses interfacial charge recombination and prolongs charge lifetime. By optimizing the contents of MgAl LDH and lignin, the device achieves a measured open circuit output voltage ( V <inf> OC </inf>) and current density ( J <inf> SC </inf>) of 96 V and 6.56 μA/cm3, with a maximum output power ( P <inf> max </inf>) of 205 μW, corresponding to a power density of 22.7 μW/cm2. We also propose a mechanistic linking of deep-level traps to prolonged charge lifetime and increased net transferable charge. The interface-engineering strategy demonstrated here paves the way for developing high-performance and sustainable biopolymer-based TENGs and motion sensors.
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Theoretically proposed stable polymorph of two-dimensional pentagonal β-PdPSe
(2023-01-04)
Dabsamut, Klichchupong
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Chatratin, Intuon
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Thanasarnsurapong, Thanasee
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Maluangnont, Tosapol
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Boonchun, Adisak
The theoretical discovery of new and stable 2D penta materials based on first-principles calculations has stimulated technological advances due to the anticipated exotic properties of such structures, which include the α and β phases of penta-NiPS. Inspired by the similarity between the theoretically proposed penta-NiPS and the experimentally synthesized (α phase) of penta-PdPSe, we propose herein the β phase of penta-PdPSe as a new penta-2D material. Comprehensive analyses indicated that β phase penta-PdPSe is thermodynamically, dynamically, mechanically, and thermally stable, similar to its NiPS analogue. It was found that β penta-PdPSe is a wide band gap semiconductor with an indirect band gap of 1.58 eV, significantly lower than 2.15 eV for the α phase. Moreover, the two polymorphs of penta-PdPSe are soft materials with 2D Young's modului of E<inf>a</inf> = 151 N m−1 and E<inf>b</inf> = 123 N m−1 for the β phase, compared with E<inf>a</inf> = 155 N m−1 and E<inf>b</inf> = 113 N m−1 for the α phase. The calculated absorption coefficient showed that β phase penta-PdPSe is acceptable for electronic and optical nanodevices.

Maluangnont, Tosapol

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