Maluangnont, Tosapol

Preferred name

Alternative Name

Maluangnont, T.

Main Affiliation

Integrated Innovative Technology

tosapol.ma@kmitl.ac.th

Now showing 1 - 10 of 10

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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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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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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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Structural, optical, and electrical properties of cellulose/titanate nanosheets composite with enhanced protection against gamma irradiation
(2023-10-01)
Maluangnont, Tosapol
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Kwamman, Tanagorn
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Pulphol, Phieraya
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Pongampai, Satana
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Charoonsuk, Thitirat
Two-dimensional (2D) materials have emerged as a promising functional filler in nanocomposites due to their unique anisotropy and resilience to harsh conditions. We report herein the use of Ti<inf>0.91</inf>O<inf>2</inf> nanosheets as a protective component against γ-irradiation to cellulose paper. The titanate nanosheets were prepared via a sequence of solid-state synthesis of lepidocrocite-type Cs<inf>0.7</inf>Ti<inf>1.825</inf>O<inf>4</inf>, proton exchange to H<inf>0.7</inf>Ti<inf>1.825</inf>O<inf>4</inf>·H<inf>2</inf>O, and exfoliation with tetrabutylammonium hydroxide. The nanosheets were incorporated into the commercial cellulose filter paper by a simple dip coating up to 0.6 mg cm−2, equivalent to 10 wt% TiO<inf>2</inf>. The nanosheets distribution was demonstrated by energy dispersive X-ray (EDX) mapping, synchrotron radiation X-ray tomographic microscopy (SRXTM), and atomic force microscopy (AFM). It is found that γ-irradiation (up to 50 kGy) destroyed the cellulose Iβ crystallinity of uncoated paper, but this is less pronounced in the cellulose/titanate nanosheets composite. This was also confirmed by the lack of a 235 nm-absorption characteristics of irradiation-induced decomposition product(s) in nanosheets-containing papers, which also exhibit UVA shielding property. The coated samples remained white while the uncoated ones were darkened with γ-irradiation. In addition, the nanosheets-coated papers showed dielectric permittivity, loss tangent, and AC conductivity which were invariant of the γ-dose, unlike those from the uncoated ones. Our work demonstrates the use of lead-free Ti<inf>0.91</inf>O<inf>2</inf> nanosheets as a γ-shielding component to slow down/prevent structural, optical, and electrical properties damages in cellulose paper, which could extend to other nature-derived materials.
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The role of γ-C2H5NO2 as a new transient liquid phase in cold sintering process of BaTiO3 composites
(2024-07-01)
Noisak, Jitrawan
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Ieamviteevanich, Pimchanok
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Charoonsuk, Thitirat
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Pakawanit, Phakkhananan
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Pinpru, Nattapong
Dielectric materials, such as barium titanate (BT)-based materials, have excellent dielectric properties but require high temperatures (above 1300 °C) for ceramic fabrication, leading to high costs and energy loss. The cold sintering process (CSP) offers a solution to these issues and is gaining worldwide attention as an innovative fabrication route. In this work, we proposed an alternative organic ferroelectric phase, gamma-glycine (γ-GC), which acts as a transient liquid phase to fabricate high-density composites with barium titanate (BT) at low temperatures through CSP. Our findings show that the density of 15γ-GC/85BT reached 96.7%±1.6% when it was sintered at 120 °C for 6 h under 10 MPa uniaxial pressure. Scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS) mappings of the composite suggested that γ-GC completely underwent the precipitation–dissolution process and, therefore, filled between BT particles. Moreover, X-ray diffraction (XRD) and Fourier-transform infrared spectroscopy (FTIR) confirmed the preservation of γ-GC without undesired phase transformation. In addition, the ferroelectric and dielectric properties of γ-GC/BT composites have been reported. The high dielectric constant (ε<inf>r</inf>) was 3600, and the low dielectric loss (tanδ) was 1.20 at 200 °C and 100 kHz for the 15γ-GC/85BT composite. The hysteresis loop showed a remanent polarization (P<inf>r</inf>) of 0.55 µC·cm-2 and a coercive field (E<inf>c</inf>) of 7.25 kV·cm-1. Our findings reaffirmed that an organic ferroelectric material (γ-GC) can act as a transient liquid phase in a CSP that can successfully and sustainably fabricate γ-GC/BT composites at low temperatures while delivering outstandingly high performance.
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Synergistic Integration of MgAl-LDH Nanosheets into Bacterial Cellulose for High-Performance Triboelectric Nanogenerators
(2025-08-04)
Mohsom, Phitchayaphorn
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Suktep, Natdanai
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Sae-Tang, Chanachot
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Pongampai, Satana
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Pakawanit, Phakkhananan
A novel nanocomposite design is presented in which magnesium aluminum layered double hydroxide (MgAl-LDH) nanosheets are synergistically integrated with bacterial cellulose (BC) to fabricate a flexible triboelectric nanogenerator (TENG). Utilizing a facile solution synthesis combined with a casting process, composite films with controlled MgAl-LDH loadings (0.25–5% v/v) were developed. The optimal composite, containing 1.5% v/v MgAl-LDH, exhibits an open-circuit voltage (V<inf>OC</inf>) of 88.5 V, a short-circuit current (I<inf>SC</inf>) of 87.7 μA, and a maximum output power (P<inf>max</inf>) of 1250 μW (power density ≈138 μW/cm2), which is > 35 times higher than that of pristine BC. Notably, this performance corresponds to a superior filler efficiency metric, demonstrating a highly effective use of the nanosheet additive compared to other reported systems. This performance enhancement is attributed to the multifunctional role of MgAl-LDH nanosheets in increasing the dielectric constant through improved interfacial conductivity and the formation of parallel microcapacitors under an induced electric field. Finite element simulations corroborate the proposed mechanism, and practical demonstrations show the nanocomposite powering 200 LEDs as well as functioning as a self-powered sensor for finger movement monitoring. These findings advance the development of high-performance, flexible energy-harvesting devices.
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A Kirigami-Engineered “Skeletal Framework” Composite for Ultralow Hysteresis and Highly Stable Strain Sensors
(2025-11-24)
Pongampai, Satana
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Chaithaweep, Kanokwan
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Pakawanit, Phakkhananan
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Charoonsuk, Thitirat
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Bongkarn, Theerachai
Wearable strain sensors are pivotal for next-generation human–machine interfaces, yet achieving high fidelity, robustness, and sustainability in a single platform remains a significant challenge. A primary obstacle is the inherent viscoelasticity of soft materials, which leads to signal drift and hysteresis. Here, we report a highly stretchable and ultrastable strain sensor fabricated through a synergistic integration of Kirigami-based structural engineering and nanocomposite material design. By introducing titanium dioxide nanotubes (TNTs) into a bacterial cellulose (BC) matrix, we create a composite with a unique internal “skeletal framework”. This framework substantially reduces viscoelastic losses, resulting in an exceptionally low hysteresis of 0.6% and ensuring robust performance with 99.4% signal stability over >10 000 cycles. Concurrently, the Kirigami-patterned structure enhances stretchability to ∼235% while the framework amplifies sensitivity 5.8-fold. The practical viability of this high-fidelity sensor is demonstrated through the precise and repeatable control of a robotic arm, where ultralow hysteresis proves more critical than raw sensitivity. The sensor’s eco-friendly, water-based fabrication aligns high-fidelity sensing with sustainable processing, presenting a clear design paradigm for engineering reliable and eco-conscious wearable electronic devices.
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Multifunctional Nanomaterials Modification of Cellulose Paper for Efficient Triboelectric Nanogenerators
(2020-05-01)
Sriphan, Saichon
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Charoonsuk, Thitirat
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Maluangnont, Tosapol
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Pakawanit, Phakkhananan
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Rojviriya, Catleya
There is a need to develop inexpensive, lightweight, and flexible high-performance triboelectric nanogenerators (TENGs) from renewable resources. Here, a multifunctional cellulose filter paper (CFP)-based TENG consisting of dielectric Ti<inf>0.8</inf>O<inf>2</inf> nanosheets (Ti<inf>0.8</inf>O<inf>2</inf> NSs) and conducting Ag nanoparticles (Ag NPs) is prepared by a simple dip coating method. The incorporation of dielectric Ti<inf>0.8</inf>O<inf>2</inf> NSs onto the CFP significantly improves charge generation, while the inclusion of Ag NPs provides an electrically conductive path for charge transportation. The presence of these fillers can be deduced from XRD, SEM, EDS, X-ray photoelectron spectroscopy, and Raman spectroscopy. Their distribution is visualized in 3D by synchrotron radiation X-ray tomography. The present CFP-based TENG provides an output voltage and current density of ≈42 V and ≈1 µA cm−2, respectively with the power density of ≈25 µW cm−2. It is capable of lighting up 40 light-emitting diode bulbs and charging a 0.22 µF capacitor to 8 V in only 5 s. The developed TENG is also capable of detecting simple human motions, i.e., finger tapping, finger rubbing, and foot trampling. This work offers a facile design of low cost yet efficient paper-based TENG by dual modification with multifunctional nanomaterials, and also demonstrates its use as a feasible power source that not only drives small electronics, but also scavenges energy from human actions.

Maluangnont, Tosapol

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