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  1. Fulltext Free standing zirconia nanotubes formation and their photocatalytic properties
    Syahriza Ismail, Nurul Izza Soaid, Suriyati Mohamed Ansari, Nurulhuda Bashirom, Monna Rozana, Tan, Wai Kian, et al.
    Malaysian Journal of Microscopy, 2016;12(1):20-23.
    MyJurnal
    In the formation of ZrO2 (zirconia) nanotubes (ZNTs) by anodisation of zirconium, a balance between chemical etching at the surface of the nanotubes and inward growth inside the nanotubes is required. This can be achieved by using fluorinated organic electrolyte like ethylene glycol with the addition of small volume of oxidant. In this work, carbonate was selected as the oxidant and NH4F as the source of fluoride for chemical etching process. Two sets of electrolytes were studied EG/fluoride/Na2CO3 and EG/fluoride/K2CO3. It appears that in the presence of carbonate evolution of gas at the anode during the anodisation process was rather severe. The gas which is likely to be CO2 was found to weaken the adherence between the oxide film with the underlying Zr foil. This induced the formation of free standing ZNTs. High Resolution Transmission Electron Microscope (HRTEM) was used to investigate the crystallinity of the nanotubes where the majority crystal phase of ZNTs was tetragonal/cubic. The ZNTs were used as photocatalysts to oxidize methyl orange dye.
  2. Anodic Ag/TiO2 nanotube array formation in NaOH/fluoride/ethylene glycol electrolyte as a photoanode for dye-sensitized solar cells
    Nyein N, Tan WK, Kawamura G, Matsuda A, Lockman Z
    Nanotechnology, 2016 Sep 02;27(35):355605.
    PMID: 27456036 DOI: 10.1088/0957-4484/27/35/355605
    Self-organized, 23 μm-thick anodic TiO2 nanotube (TNT) arrays were formed in sodium hydroxide/fluoride/ethylene glycol (EG) electrolyte at 60 V for 60 min. The presence of sodium hydroxide (NaOH) in the fluoride/EG electrolyte accelerates the formation of the TiO2 nanotube arrays. The anodic film was then decorated with silver nanoparticles (Ag NPs) by the photodeposition process and used as a photoanode in a rear-side-illuminated dye-sensitized solar cell. The Ag NPs decorated TNT arrays, with the former having diameters of 10-30 nm formed from 0.2 M of Ag-precursor solution and exhibiting the highest photoconversion efficiency (η) of 3.7% and a short-circuit current density of 12.2 mA cm(-2) compared to η = 3% and short-circuit current density of 9.1 mA cm(-2) for a sample without Ag NPs. The increase in η is thought to be due to the surface plasmon resonance and excess electrons from the nanoparticles.
  3. Facile Fabrication of Plasmonic Enhanced Noble-Metal-Decorated ZnO Nanowire Arrays for Dye-Sensitized Solar Cells
    Tan WK, Muto H, Ito T, Kawamura G, Lockman Z, Matsuda A
    J Nanosci Nanotechnol, 2020 Jan 01;20(1):359-366.
    PMID: 31383179 DOI: 10.1166/jnn.2020.17223
    Novel decoration of high aspect ratio zinc oxide nanowires (ZnO NWs) with noble metals such as Ag and Au nanoparticles (NPs) was demonstrated in this work. A facile method of chemical deposition with good controllability, as well as good homogeneity would be a huge advantage towards large scale fabrication. The highlight of this work is the feasibility of multiple component decoration such as a hybrid (co-exist) Ag-Au NPs decorated ZnO NWs formation that could be beneficial towards the development of nanoarchitectured materials with the most desired properties. The local surface plasmon effect (LSPR) of Ag and Au NPs were confirmed using extinction spectra and significant photoelectrochemical conversion efficiency (PCE) enhancement of dye-sensitized solar cells (DSSCs) was achieved. The Ag-NPs and hybrid Ag-Au NPs decorated ZnO NWs marked an impressive 125 and 240% efficiency improvement against pure ZnO NWs. The improved dye light extinction resulted from the LSPR effect that had enabled greater electron generation leading to improved PCE. As the complex design of oxides' nanoarchitectures have reached a point of saturation, this novel method would enable further enhancement in their photoelectrochemical properties through decoration with noble metals via a simple chemical deposition route.
  4. Nanoporous anodic Nb2O5 with pore-in-pore structure formation and its application for the photoreduction of Cr(VI)
    Alias N, Hussain Z, Tan WK, Kawamura G, Muto H, Matsuda A, et al.
    Chemosphere, 2021 Nov;283:131231.
    PMID: 34144283 DOI: 10.1016/j.chemosphere.2021.131231
    An anodic film with a nanoporous structure was formed by anodizing niobium at 60 V in fluorinated ethylene glycol (fluoride-EG). After 30 min of anodization, the anodic film exhibited a "pore-in-pore" structure; that is, there were smaller pores growing inside larger pores. The as-anodized film was weakly crystalline and became orthorhombic Nb2O5 after heat treatment. The energy band gap of the annealed nanoporous Nb2O5 film was 2.9 eV. A photocatalytic reduction experiment was performed on Cr(VI) under ultraviolet (UV) radiation by immersing the nanoporous Nb2O5 photocatalyst in a Cr(VI) solution at pH 2. The reduction process was observed to be very slow; hence, ethylenediaminetetraacetic acid (EDTA) was added as an organic hole scavenger, which resulted in 100% reduction after 45 min of irradiation. The photocatalytic reduction experiment was also performed under visible light, and findings showed that complete reduction achieved after 120 min of visible light exposure.
  5. Fulltext Magnetically recoverable magnetite-reduced graphene oxide as a demulsifier for surfactant stabilized crude oil-in-water emulsion
    Yau XH, Khe CS, Mohamed Saheed MS, Lai CW, You KY, Tan WK
    PLoS One, 2020;15(4):e0232490.
    PMID: 32353051 DOI: 10.1371/journal.pone.0232490
    Oily wastewater, especially water-oil emulsion has become serious environmental issue and received global attention. Chemical demulsifiers are widely used to treat oil-water emulsion, but the toxicity, non-recyclable and non-environmental friendly characteristic of chemical demulsifiers had limited their practical application in oil-water separation. Therefore, it is imperative to develop an efficient, simple, eco-friendly and recyclable demulsifiers for breaking up the emulsions from the oily wastewater. In this study, a magnetic demulsifier, magnetite-reduced graphene oxide (M-rGO) nanocomposites were proposed as a recyclable demulsifier to break up the surfactant stabilized crude oil-in-water (O/W) emulsion. M-rGO nanocomposites were prepared via in situ chemical synthesis by using only one type Fe salt and GO solid as precursor at room temperature. The prepared composites were fully characterized by various techniques. The effect of demulsifier dosage and pH of emulsion on demulsification efficiency (ED) has been studied in detailed. The demulsification mechanism was also proposed in this study. Results showed that M-rGO nanocomposites were able to demulsify crude O/W emulsion. The ED reaches 99.48% when 0.050 wt.% of M-rGO nanocomposites were added to crude O/W emulsion (pH = 4). Besides, M-rGO nanocomposites can be recycled up to 7 cycles without showing a significant change in terms of ED. Thus, M-rGO nanocomposite is a promising demulsifier for surfactant stabilized crude O/W emulsion.
  6. Fulltext Formation of Dense and High-Aspect-Ratio Iron Oxide Nanowires by Water Vapor-Assisted Thermal Oxidation and Their Cr(VI) Adsorption Properties
    Budiman F, Tan WK, Kawamura G, Muto H, Matsuda A, Abdul Razak K, et al.
    ACS Omega, 2021 Oct 26;6(42):28203-28214.
    PMID: 34723018 DOI: 10.1021/acsomega.1c04280
    Coral-like and nanowire (NW) iron oxide nanostructures were produced at 700 and 800 °C, respectively, through thermal oxidation of iron foils in air- and water vapor-assisted conditions. Water vapor-assisted thermal oxidation at 800 °C for 2 h resulted in the formation of highly crystalline α-Fe2O3 NWs with good foil surface coverage, and we propose that their formation was due to a stress-driven surface diffusion mechanism. The Cr(VI) adsorption property of an aqueous solution on α-Fe2O3 NWs was also evaluated after a contact time of 90 min. The NWs had a removal efficiency of 97% in a 225 mg/L Cr(VI) solution (pH 2, 25 °C). The kinetic characteristic of the adsorption was fitted to a pseudo-second-order kinetic model, and isothermal studies indicated that the α-Fe2O3 NWs exhibited an adsorption capacity of 66.26 mg/g. We also investigated and postulated a mechanism of the Cr(VI) adsorption in an aqueous solution of α-Fe2O3 NWs.
  7. Fulltext Characterization of Fungal Foams from Edible Mushrooms Using Different Agricultural Wastes as Substrates for Packaging Material
    Majib NM, Sam ST, Yaacob ND, Rohaizad NM, Tan WK
    Polymers (Basel), 2023 Feb 10;15(4).
    PMID: 36850157 DOI: 10.3390/polym15040873
    Agricultural wastes and leaves, which are classified as lignocellulosic biomass, have been used as substrates in the production of fungal foams due to the significant growth of the mushroom industry in recent years. Foam derived from fungi can be utilized in a variety of industrial applications, including the production of packaging materials. Here, white oyster mushrooms (Pleurotus florida) and yellow oyster mushrooms (Pleurotus citrinopileatus) were cultivated on rice husk, sawdust, sugarcane bagasse, and teak leaves. Fungal foams were produced after 30 days of incubation, which were then analyzed using scanning electron microscopy (SEM), thermal analysis (TGA), and chemical structure using Fourier-transform infrared spectroscopy. Mechanical testing examined the material's hardness, resilience, and springiness, and water absorption tests were used to determine the durability of the fungal foams. Our findings demonstrated that fungal foams made from rice husk and teak leaves in both mycelium species showed better mechanical properties, thermal stability, and minimal water absorption compared to the other substrates, and can thus have great potential as efficient packaging materials.
  8. Photoreduction of Cr(VI) in wastewater by anodic nanoporous Nb2O5 formed at high anodizing voltage and electrolyte temperature
    Alias N, Hussain Z, Tan WK, Kawamura G, Muto H, Matsuda A, et al.
    Environ Sci Pollut Res Int, 2022 Aug;29(40):60600-60615.
    PMID: 35426025 DOI: 10.1007/s11356-022-20005-7
    In this study, nanoporous anodic film was produced by anodization of niobium, Nb in a fluoride ethylene glycol electrolyte. The effect of anodization voltage and electrolyte temperature was studied to find an optimum condition for circular, ordered, and uniform pore formation. The diameter of the pores was found to be larger when the applied voltage was increased from 20 to 80 V. The as-anodized porous film was also observed to comprise of nanocrystallites which formed due to high field-induced crystallization. The nanocrystallites grew into orthorhombic Nb2O5 after post-annealing treatment. The Cr(VI) photoreduction property of both the as-anodized and annealed Nb2O5 samples obtained using an optimized condition (anodization voltage: 60 V, electrolyte temperature: 70 °C) was compared. Interestingly, the as-anodized Nb2O5 film was found to display better photoreduction of Cr(VI) than annealed Nb2O5. However, in terms of stability, the annealed Nb2O5 presented high photocatalytic efficiency for each cycle whereas the as-anodized Nb2O5 showed degradation in photocatalytic performance when used continually.
  9. Fulltext Ag nanoparticle-deposited TiO2 nanotube arrays for electrodes of Dye-sensitized solar cells
    Kawamura G, Ohmi H, Tan WK, Lockman Z, Muto H, Matsuda A
    Nanoscale Res Lett, 2015;10:219.
    PMID: 26019696 DOI: 10.1186/s11671-015-0924-1
    ABSTRACT: Dye-sensitized solar cells composed of a photoanode of Ag nanoparticle (NP)-deposited TiO2 nanotube (TNT) arrays were fabricated. The TNT arrays were prepared by anodizing Ti films on fluorine-doped tin oxide (FTO)-coated glass substrates. Efficient charge transportation through the ordered nanostructure of TNT arrays should be carried out compared to conventional particulate TiO2 electrodes. However, it has been a big challenge to grow TNT arrays on FTO glass substrates with the lengths needed for sufficient light-harvesting (tens of micrometers). In this work, we deposited Ag nanoparticles (NPs) on the wall of TNT arrays to enhance light-harvesting property. Dye-sensitized solar cells with these Ag NP-deposited TNT arrays yielded a higher power conversion efficiency (2.03 %) than those without Ag NPs (1.39 %).

    PACS CODES: 06.60.Ei Sample preparation, 81.05.Bx Metals, Semimetals, Alloys, 81.07.De Nanotubes.

  10. Fulltext Degradation of Diazo Congo Red Dye by Using Synthesized Poly-Ferric-Silicate-Sulphate through Co-Polymerization Process
    Zainudin NF, Sam ST, Wong YS, Ismail H, Walli S, Inoue K, et al.
    Polymers (Basel), 2023 Jan 03;15(1).
    PMID: 36616587 DOI: 10.3390/polym15010237
    The ability of poly-ferric-silicate-sulphate (PFSS) synthesized via a co-polymerization process has been applied for the removal of diazo Congo red dye. A novel degradation pathway of diazo Congo red dye by using PFSS is proposed based on LC-MS analysis. Diazo Congo red dye was successfully removed using synthesized PFSS at lower coagulant dosages and a wider pH range, i.e., 9 mg/L from pH 5 to 7, 11 mg/L at pH 9, and 50 mg/L at pH 11. The azo bond cleavage was verified by the UV-Vis spectra of diazo Congo red-loaded PFSS and FTIR spectra which showed disappearance of the peak at 1584 cm-1 for -N=N- stretching vibrations. The synchronized results of UV-Vis spectra, FTIR, and the LC-MS analysis in this study confirmed the significance of the Si and Fe bond in PFSS towards the degradation of diazo Congo red dye. The successfully synthesized PFSS coagulant was characterized by FTIR, SEM, TEM, and HRTEM analysis. From this analysis, it was proven that PFSS is a polycrystalline material which is favorable for the coagulation-flocculation process. Based on all these findings, it was established that synthesized PFSS can be employed as a highly efficient polymeric coagulant for the removal of dye from wastewater.
  11. Formation of grassy TiO2 nanotube thin film by anodisation in peroxide electrolyte for Cr(VI) removal under ultraviolet radiation
    Taib MAA, Alias N, Jaafar M, Razak KA, Tan WK, Shahbudin IP, et al.
    Nanotechnology, 2020 Oct 23;31(43):435605.
    PMID: 32640434 DOI: 10.1088/1361-6528/aba3d8
    Arrays of TiO2 nanotubes (TiO2 NTs) with grassy surfaces were observed on titanium foil anodised at 60 V in fluorinated ethylene glycol (EG) with added hydrogen peroxide (H2O2). The grassy surface was generated by the chemical etching and dissolution of the surface of the TiO2 NTs walls, which was accelerated by the temperature increase on the addition of H2O2 . Upon annealing at 600 °C, the grassy part of the TiO2 NTs was found to consist of mostly anatase TiO2 whereas the bottom part of the anodic oxide comprised a mixture of anatase and rutile TiO2. The TiO2 NTs were then used to reduce hexavalent chromium (Cr(VI)) under ultraviolet radiation. They exhibited a rather efficient photocatalytic effect, with 100% removal of Cr(VI) after 30 min of irradiation. The fast removal of Cr(VI) was due to the anatase dominance at the grassy part of the TiO2 NTs as well as the higher surface area the structure may have. This work provides a novel insight into the photocatalytic reduction of Cr(VI) on grassy anatase TiO2 NTs.
  12. Rapid Nucleation of Reduced Graphene Oxide-Supported Palladium Electrocatalysts for Methanol Oxidation Reaction
    Ng JC, Tan CY, Ong BH, Matsuda A, Basirun WJ, Tan WK, et al.
    J Nanosci Nanotechnol, 2019 Nov 01;19(11):7236-7243.
    PMID: 31039881 DOI: 10.1166/jnn.2019.16717
    Small sized electrocatalysts, which can be obtained by rapid nucleation and high supersaturation are imperative for outstanding methanol oxidation reaction (MOR). Conventional microwave synthesis processes of electrocatalysts include ultrasonication, stirring, pH adjustment, and microwave irradiation of the precursor mixture. Ethylene glycol (EG), which serves as a reductant and solvent was added during the ultrasonication or stirring stage. However, this step and pH adjustment resulted in unintended multi-stage gradual nucleation. In this study, the microwave reduction approach was used to induce rapid nucleation and high supersaturation in order to fabricate small-sized reduced graphene oxide-supported palladium (Pd/rGO) electrocatalysts via the delayed addition of EG, elimination of the pH adjustment step, addition of sodium carbonate (Na₂CO₃), prior microwave irradiation of the EG mixed with Na₂CO₃, and addition of room temperature precursor mixture. Besides its role as a second reducing agent, the addition of Na₂CO₃ was primarily intended to generate an alkaline condition, which is essential for the high-performance of electrocatalysts. Moreover, the microwave irradiation of the EG and Na₂CO₃ mixture generated highly reactive free radicals that facilitate rapid nucleation. Meanwhile, the room temperature precursor mixture increased supersaturation. Results showed improved electrochemically active surface area (78.97 m² g-1, 23.79% larger), MOR (434.49 mA mg-1, 37.96% higher) and stability.
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