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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‐Cu2O/n‐g‐C3N4 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. [ABSTRACT FROM AUTHOR]

Triboelectric nanogenerators (TENGs) are crucial for applications such as smart sensors and bio-electronics. In the current work, we aimed for improved performance of TENGs with incorporation of BaTiO3 powder, which is known for its strong ferroelectric properties, combining it with epoxy resin to improve the flexibility of our devices. We observed that our TENGs can operate for over 24 000 cycles with no degradation of function. Additionally, we improved the electrical performance of the TENGs by incorporating various aluminum concentrations that change the electronic properties in the form of mixed epoxy resin, BaTiO3, and Al nanopowders. To identify the optimum conditions for the best performance, we analyzed the electrical characteristics and material properties by employing scanning electron microscopy, energy dispersive x-ray spectroscopy, and x-ray diffractometry characterization techniques. Our findings suggest that this innovative combination of materials and optimization techniques can significantly improve the performance of TENGs, making them ideal for practical applications in various fields, such as low-power electronics, environmental monitoring and healthcare. Moreover, these enhanced TENGs can serve as sustainable and dependable energy sources for various applications. [ABSTRACT FROM AUTHOR]

Triboelectric nanogenerators (TENG) with great performance and biodegradability are desired for the expansion of novel medical devices and wearable electronics. The present study aims at the preparation of natural silk in the form of silk fibroin (SF) film for utilization in TENG and further improving its output efficiency by embedding organic-piezoelectric gamma-glycine (γ-gly) amino acid to be a hybrid-organic piezoelectric/triboelectric nanogenerator (HO-P/TENG). The attenuated total reflectance infrared spectroscopy (ATR-IR) results demonstrated the N-H, C = O, and C-N bonding for SF and SF/γ-gly, confirming its dominant effect with a strong electron-donating tendency from those amino groups. The scanning electron microscope (SEM) and synchrotron radiation X-ray tomographic microscopy (SR-XTM) images show good dispersibility of incorporated γ-gly on the surface and also inside the SF matrix relating to its content to improve the electrical performance homogeneously. By fabricating the device in the vertical contact-separation mode, the present SF/γ-gly HO-P/TENG at 15 wt% provides the maximum output voltage (VOC) and current (ISC) of 81 V and 121 μA with a maximum output power (Pmax) of 205 μW at the external load resistance of 5 MΩ. This SF-based HO-P/TENG has the advantage of being cost-effective with simple fabrication, demonstrating great promise for practical uses. [ABSTRACT FROM AUTHOR]

Surface charge density is a key factor that greatly enhances the performance of a natural-based triboelectric nanogenerator (TENG), which is essential for future sustainable sensing and harvesting devices. This work introduced a conductive interlayer between a main frictional layer and electrode. This approach can suppress the charge recombination rate and improve the amount of charges produced during the triboelectrification process. Bacterial cellulose (BC) film was selected as a main frictional layer for the TENG. A conductive nanomaterial, i.e. silver flake, was incorporated into the BC film as an intermediate layer for enhancing TENG performance. As firstly reported, the maximum electrical outputs for the multi-layer BC structure could be found when using silver flake/BC composite (ratio 1:5) as an intermediate layer, which has 122 V and 8.2 µA of output voltage and current, respectively. This is higher than the output voltage and current of a single layer BC TENG by approximately 3 and 8 times, respectively. The maximum output power of ∼440 µW is achieved by connecting with a load resistor of ∼10 MΩ. This demonstrates an efficient strategy for designing a high performance energy harvester by adding an intermediate layer for the target of practical purposes in sustainable systems. [ABSTRACT FROM AUTHOR]

Polydopamine/Ag (PDA/Ag) nanoparticles were synthesized for methylene blue (MB) removal from aqueous solution as a model dye. These particles were prepared in a modified literature procedure in which polydopamine (PDA) nanoparticles were first prepared via the oxidative polymerization of dopamine (DA) under alkaline conditions in the presence of oxygen. Subsequently, nanoparticulate PDA/Ag was accessed from direct reduction of silver precursor [Ag(NH3)2]+ ions by catechol amino groups in the PDA structure to form Ag nanoparticles (AgNPs) fixed on the PDA surface. Confirmation of the formation of the PDA and PDA/Ag nanoparticles, plus characterization of their surface morphologies was achieved. In the MB adsorption studies, the various factors affecting the dye adsorption and thermodynamic parameters were investigated in detail. This adsorption process can be described well by the Langmuir model. In order to gain a deeper molecular insight into this process, we investigated some possible local model structures of PDA/Ag nanoparticles and MB interaction with these structures using density functional theory (DFT) calculations. The results indicated that the adsorption energies (Eads) of MB on the PDA/Ag nanoparticles were higher than the Eads of MB on PDA nanoparticles, which was consistent with the experimental results. Our results provide a significant new finding for the role of Ag nanoparticles in the MB adsorption process on PDA/Ag nanoparticles. Readily accessible nanoparticulate PDA/Ag was shown to be a highly effective adsorbent for MB from aqueous solution and thus has significant potential for applications in wastewater dye removal. [ABSTRACT FROM AUTHOR]

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 Ti2NbO7 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.% Ti2NbO7 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 Ti2NbO7 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 Ti2NbO7 NSs. [ABSTRACT FROM AUTHOR]

The focus of this study is the fabrication of innovative and sustainable ceramic-based geopolymer with improved low temperatures performances. Kaolin was mixed with liquid sodium silicate (Na2SiO3) and 12M of sodium hydroxide (NaOH) solution using alkali activator ratio of 0.24 and solid-to-liquid ratio of 1:1 to synthesize kaolin geopolymer. The effect of the sintering profile on the microstructure, pore evolution and flexural strength were investigated. The heating exposure aided consolidation and created a fairly uniform microstructure, resulting in a smooth surface texture. In comparison to the unheated geopolymer, 3D pore distribution showed a significant increase in the range size of ~30 µm with the appearance of isolated and intergranular pores. The flexural strength at 1200 °C with a heating rate of 5 °C/min and was increased by 146.4% to 85.4 MPa, as compared to the heating rate of 2 °C/min. The sintering process has an impact on the final microstructure formation thus improving the characteristic of geopolymer-based nepheline ceramic. [ABSTRACT FROM AUTHOR]

Alkali-activated cement (AAC) produced with metakaolin and black rice husk ash was investigated. The characteristics, physical properties, and thermal properties were investigated. Porosity assessments were carried out using synchrotron radiation X-ray tomographic microscopy (XTM). The results revealed that the concentration of NaOH solution and Na2SiO3 solution was the key parameter which affected the morphology and properties of AAC. Particle-structures and prolonged structures were formed when using NaOH as an activator. However, stacked plate-like structures were observed when using Na2SiO3 together with NaOH. The amorphous phases of N-A-S-H gel and geopolymer were formed. XTM profiles showed that the pore volume decreased with increasing NaOH solution concentration and Na2SiO3 contents. The 3D images illustrated that the pore structures were occupied by pores less than 50 µm in size. Pore connections within the range of 0–50 µm were the main parameter which controlled the thermal and physical properties. [ABSTRACT FROM AUTHOR]

This paper elucidates the influence of borax decahydrate addition on the flexural and thermal properties of 10 mm thin fly ash/ladle furnace slag (FAS) geopolymers. The borax decahydrate (2, 4, 6, and 8 wt.%) was incorporated to produce FAB geopolymers. Heat treatment was applied with temperature ranges of 300 °C, 600 °C, 900 °C, 1000 °C and 1100 °C. Unexposed FAB geopolymers experienced a drop in strength due to a looser matrix with higher porosity. However, borax decahydrate inclusion significantly enhanced the flexural performance of thin geopolymers after heating. FAB2 and FAB8 geopolymers reported higher flexural strength of 26.5 MPa and 47.8 MPa, respectively, at 1000 °C as compared to FAS geopolymers (24.1 MPa at 1100 °C). The molten B2O3 provided an adhesive medium to assemble the aluminosilicates, improving the interparticle connectivity which led to a drastic strength increment. Moreover, the borax addition reduced the glass transition temperature, forming more refractory crystalline phases at lower temperatures. This induced a significant strength increment in FAB geopolymers with a factor of 3.6 for FAB8 at 900 °C, and 4.0 factor for FAB2 at 1000 °C, respectively. Comparatively, FAS geopolymers only achieved 3.1 factor in strength increment at 1100 °C. This proved that borax decahydrate could be utilized in the high strength development of thin geopolymers. [ABSTRACT FROM AUTHOR]

Ancient potteries found at Ban Muang Bua, located in northeastern Thailand, associate with Thung Kula Ronghai culture. Most of them are products used in daily life and grave goods. The potsherds were examined using techniques based on X-ray spectroscopy. Elemental composition and morphology were analyzed using proton-induced X-ray emission spectroscopy (PIXE) and scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM-EDS). Three-dimensional analysis was performed using X-ray tomographic microscopy based on synchrotron radiation (SR XTM). Irregular plate-like particles of composites with a wide range of size distribution were found in the potsherds. The major (O, Si, and Al), minor (C, Fe, Ca, and K), and trace elements (P, S, Ti, Na, Mg, and Zn) which were observed can provide the information about raw materials and production of pottery. The 3D tomographic images show the internal feature of these samples. The combination of SEM-EDS, PIXE, and SR XTM is a powerful tool for archaeological research especially in terms of composition and internal structure. The results imply that the raw materials of pottery were sandy soil derived from marine sands, clays, and salt deposits that were mostly iron-rich-kaolin clay. The production was carried out with low firing temperatures (~600–900 °C) in open-air kilns. [ABSTRACT FROM AUTHOR]

Silver diamine nitrate (SDN) is expected to help control caries similar to silver diamine fluoride (SDF). The aim of this study was to determine the mineral precipitation in demineralized dentin and the cytotoxicity of SDN and SDF to dental pulp cells. Demineralized dentin specimens were prepared, and SDF, SDN, or water (control) was applied. The specimens were then remineralized in simulated body fluid for 2 weeks. The mineral precipitation in the specimens was examined using FTIR-ATR, SEM-EDX, and synchrotron radiation X-ray tomographic microscopy (SRXTM). Additionally, the cytotoxicity of SDF and SDN to human dental pulp stem cells was analyzed using an MTT assay. The increase in FTIR spectra attributable to apatite formation in demineralized dentin in the SDF group was significantly higher compared to the SDN and control groups (p < 0.05). Dentinal tubule occlusion by the precipitation of silver salts was detected in both SDF and SDN groups. The mineral density as shown in SRXTM images and cytotoxicity of both SDN and SDF groups were comparable (p > 0.05). In conclusion, SDF demonstrated superior in vitro apatite formation compared to SDN. However, the degree of mineral precipitation and cytotoxic effects of both were similar. [ABSTRACT FROM AUTHOR]

Owing to their structural advantages over bulk polymers, porous 3D substrates possess immense potential in triboelectric energy generation. This work reports the effective effort to fabricate the porous structure of polydimethylsiloxane, also known as the sponge-PDMS, by a simple template method. The sodium chloride salt from commodity product is used to create the 300 μm size of pores within the PDMS elastomeric layers, turning affects to the mechanical deformability of the triboelectric nanogenerator (TENG). The inner face of those pores is composited with the PVDF-HFP particles as a piezoelectric fillers. The presence of those fillers can be confirmed and their distribution within porous PDMS is 3D visualized by the synchrotron radiation X-ray tomography. The spatial distribution of the PVDF-HFP made it possible to fabricate the piezo-embedded macroporous TENG with high output power of 7.84 μW, giving over 2-fold enhancement, compared with the sponge-PDMS and even more when compared with the flat PDMS film under the same mechanical force. [ABSTRACT FROM AUTHOR]

This research investigated the physicochemical properties, bioactive compounds, and microstructure of brown rice (BR) and non-parboiled and parboiled germinated brown rice (GBR and PGBR). The GBR and PGBR were treated by sun, hot-air oven, or infrared irradiation (IR) drying. The results showed that IR drying enhanced the bioactive compounds of non-parboiled GBR, including γ-aminobutyric acid, α-tocopherol, and total phenolic compounds, while γ-oryzanol and antioxidant activity were comparable to BR. Meanwhile, IR drying significantly improved the head rice yield (HRY) of PGBR while reducing fissured grains. Parboiling also affected the color values of rice grains, suggesting the diffusion of husk color into endosperm and the formation of brown polymers by the Maillard reaction. In addition, IR drying altered the internal structure of rice grains, resulting in abundant intercellular voids. Specifically, the IRdried non-parboiled GBR significantly enhanced essential bioactive compounds and improved HRY while maintaining the color of standard BR. [ABSTRACT FROM AUTHOR]

Local structure of lead zinc niobate (PZN) ceramic, synthesized via B-site oxide precursor route in atmospheric pressure, was investigated using synchrotron x-ray absorption spectroscopy (XAS) technique. The x-ray absorption near-edge structure (XANES) simulation was first carried out. The XANES simulation results indicate that the PZN ceramic is in pyrochlore phase having Zn2+ substituted on Nb5+ site. Afterwards, the extended x-ray absorption fine structure (EXAFS) analysis was performed to extract the bond length information between Zn2+ and its neighboring atoms. From the EXAFS fitting, the bond length between Zn2+ and Pb2+ in the pyrochlore phase was found to be longer than the previously reported bond length in the perovskite phase. Further, with the radial distribution information of Zn2+'s neighboring atoms, the formation energies along the precursor-to-pyrochlore and precursor-to-perovskite reaction paths were calculated using the density functional theory (DFT). The calculated results show that the formation energy of the perovskite phase is noticeably higher than that of the pyrochlore phase, which is influenced by the presence of energetic Pb2+ lone pair, as the perovskite phase has shorter Zn2+ to Pb2+ bonding. This therefore suggests the steric hindrance of Pb2+ lone pair and the mutual interactions between Pb2+ lone pair and Zn2+ are main causes of the instability of lead zinc niobate in the perovskite structure and confirm the efficacy of XAS and DFT analysis in revealing local structural details of complex pyrochlore materials. [ABSTRACT FROM AUTHOR]

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 Ti0.8O2 nanosheets (Ti0.8O2 NSs) and conducting Ag nanoparticles (Ag NPs) is prepared by a simple dip coating method. The incorporation of dielectric Ti0.8O2 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. [ABSTRACT FROM AUTHOR]