ORCID Profile
0000-0002-4354-1857
Current Organisation
Kyungpook National University
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Publisher: Elsevier BV
Date: 08-2016
Publisher: Wiley
Date: 27-02-2007
DOI: 10.1002/APP.25938
Publisher: American Scientific Publishers
Date: 07-2014
Publisher: MDPI AG
Date: 10-11-2020
DOI: 10.3390/MA13225072
Abstract: Titanium dioxide (TiO2), the golden standard among the photocatalysts, exhibits a varying level of photocatalytic activities (PCA) amongst the synthetically prepared and commercially available products. For commercial applications, superior photoactivity and cost-effectiveness are the two main factors to be reckoned with. This study presents the development of simple, cost-effective post-treatment processes for a less costly TiO2 to significantly enhance the PCA to the level of expensive commercial TiO2 having demonstrated superior photoactivities. We have utilized sequential calcination and ball milling (BM) post-treatment processes on a less-costlier KA100 TiO2 and demonstrated multi-fold (nearly 90 times) enhancement in PCA. The post-treated KA100 s les along with reference commercial s les (P25, NP400, and ST01) were well-characterized by appropriate instrumentation and evaluated for the PCA considering acetaldehyde photodegradation as the model reaction. Lattice parameters, phase composition, crystallite size, surface functionalities, titanium, and oxygen electronic environments were evaluated. Among post-treated KA100, the s le that is subjected to sequential 700 °C calcination and BM (KA7-BM) processes exhibited 90-fold PCA enhancement over pristine KA100 and the PCA-like commercial NP400 (pure anatase-based TiO2). Based on our results, we attribute the superior PCA for KA7-BM due to the smaller crystallite size, the co-existence of mixed anatase-srilankite-rutile phases, and the consequent multiphase heterojunction formation, higher surface area, lattice disorder/strain generation, and surface oxygen environment. The present work demonstrates a feasible potential for the developed post-treatment strategy towards commercial prospects.
Publisher: Wiley
Date: 08-07-2007
DOI: 10.1002/APP.26601
Publisher: MDPI AG
Date: 16-09-2020
DOI: 10.3390/NANO10091854
Abstract: Titanium dioxide (TiO2) has been extensively investigated in interdisciplinary research (such as catalysis, energy, environment, health, etc.) owing to its attractive physico-chemical properties, abundant nature, chemical/environmental stability, low-cost manufacturing, low toxicity, etc. Over time, TiO2-incorporated building/construction materials have been utilized for mitigating potential problems related to the environment and human health issues. However, there are challenges with regards to photocatalytic efficiency improvements, lab to industrial scaling up, and commercial product production. Several innovative approaches/strategies have been evolved towards TiO2 modification with the focus of improving its photocatalytic efficiency. Taking these aspects into consideration, research has focused on the utilization of many of these advanced TiO2 materials towards the development of construction materials such as concrete, mortar, pavements, paints, etc. This topical review focuses explicitly on capturing and highlighting research advancements in the last five years (mainly) (2014–2019) on the utilization of various modified TiO2 materials for the development of practical photocatalytic building materials (PBM). We briefly summarize the prospective applications of TiO2-based building materials (cement, mortar, concretes, paints, coating, etc.) with relevance to the removal of outdoor/indoor NOx and volatile organic compounds, self-cleaning of the surfaces, etc. As a concluding remark, we outline the challenges and make recommendations for the future outlook of further investigations and developments in this prosperous area.
Publisher: American Scientific Publishers
Date: 07-2014
Publisher: MDPI AG
Date: 04-03-2020
DOI: 10.3390/NANO10030456
Abstract: We report the detailed microstructural, morphological, optical and photocatalytic studies of graphene (G) and manganese (Mn) co-doped titanium dioxide nanowires (TiO2(G–Mn) NWs) prepared through facile combined electrospinning–hydrothermal processes. The as-prepared s les were thoroughly characterized using X-ray diffraction (XRD), transmission electron microscopy, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and diffuse reflectance spectroscopy (DRS). XRD studies reveal the formation of mixed anatase-rutile phases or rutile phase depending on the dopant (Mn) precursor concentrations in the electrospinning dope and calcination temperature. The evaluation of lattice parameters revealed that the incorporation of Mn species and carbon atoms in to the lattice of anatase or rutile TiO2 could occur through substituting the sites of oxygen atoms. XPS results confirm the existence of Mn2+/Mn3+ within the TiO2 NW. Raman spectroscopy provides the evidence for structural modification because of the graphene inclusion in TiO2 NW. The optical band gap of G–Mn including TiO2 is much lower than pristine TiO2 as confirmed through UV-vis DRS. The photocatalytic activities were evaluated by nitric oxide (NOx) degradation tests under visible light irradiation. Superior catalytic activity was witnessed for rutile G–Mn-co-doped TiO2 NW over their anatase counterparts. The enhanced photocatalytic property was discussed based on the synergistic effects of doped G and Mn atoms and explained by plausible mechanisms.
Publisher: Wiley
Date: 31-03-2006
DOI: 10.1002/POLA.21451
Publisher: Springer Science and Business Media LLC
Date: 15-04-2006
Publisher: MDPI AG
Date: 22-02-2021
Abstract: In recent years, there has been a great demand for the rational design and development of novel catalytic materials at the nanoscale (1–100 nm), with a view to more accurately and efficiently control reaction pathways due to their high surface area and intrinsic properties [...]
Publisher: Elsevier BV
Date: 02-2015
DOI: 10.1016/J.JHAZMAT.2014.09.014
Abstract: In this work, a new hybrid nanocatalyst, namely titanium dioxide (TiO2) composite nanowires, encapsulated with graphene (G) and palladium nanoparticles (Pd NPs) (designated as G-Pd@TiO2-CNWs), was prepared. In preparing the nanowires, a combination of electrospinning and hydrothermal approaches was employed. The visible-light-driven photocatalytic performance of G-Pd@TiO2-CNWs was investigated using the reduction of 4-nitrophenol (4-NP) as a model reaction. The results showed that G-Pd@TiO2-CNWs converted nearly 100% of 4-NP under visible light irradiation. The reaction kinetics of the photocatalytic reduction of 4-NP was studied by UV-vis spectrophotometry and the apparent rate constant was determined and compared with those for other supported TiO2 catalysts. Furthermore, the spent G-Pd@TiO2-CNWs could be recovered by simple centrifugation and reused. The work is expected to shed new light on the development of G-incorporated hybrid nanostructures for harvesting light energy and on the development of new photocatalysts for the removal of environmental pollutants.
Publisher: Elsevier BV
Date: 03-2015
Publisher: Elsevier BV
Date: 08-2013
DOI: 10.1016/J.BIOS.2013.02.036
Abstract: A "modular approach" has been demonstrated for the preparation of nanodiamond (ND) based sponges (NS) with entrapped enzyme (horseradish peroxidase, HRP) (ND-NS(HRP)) and utilization as an electrochemical probe for detection of hydrogen peroxide (H₂O₂). ND-NS comprises ND, porous poly(aniline)-poly(2-acrylamido 2-methyl propane sulfonic acid) (PANI-PAMPSA) network and entrapped HRP. Field emission scanning electron microscope image of ND-NS(HRP) reveals sponge like suprastructure comprising interconnected nanospheres with numerous openings inholes/cavities. The entrapped HRP in ND-NS exhibits effective direct electron transfer with an electron transfer rate constant of 1.85 s(-1). ND-NS(HRP) exhibited excellent bioelectrocatalytic reduction of hydrogen peroxide (H₂O₂) with a wide linear concentration range (1-45 mM), quick response (5s), high sensitivity (129.6 μAM(-1)) and low detection limit 59 μM (S/N=3).
Publisher: Institute of Electrical and Electronics Engineers (IEEE)
Date: 08-2013
Publisher: American Scientific Publishers
Date: 09-2007
DOI: 10.1166/JNN.2007.692
Abstract: Poly(ortho-toluidine) (POT)-gold (Au) and palladium (Pd) composite nanospheres were successfully synthesized by the reaction of o-toluidine with the corresponding metal (Au or Pd) colloidal solution through self-assembly process in the presence of dodecylbenzenesulfonic acid (DBSA), which acts as both a dopant and surfactant, and ammonium peroxydisulfate as an oxidizing agent. The composites (POT-DBSA/Au or Pd) were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier transform infrared (FTIR) spectroscopy, UV-Visible (UV-Vis) spectroscopy, and electrical conductivity measurements. TEM images of the nanocomposites reveal that metal (Au or Pd) nanoparticles were well dispersed on POT spheres. TGA and XRD results show that the composites exhibit high thermal stability and are more crystalline compared with pristine POT. It was found that the electrical conductivity of the POT-DBSA/Au or Pd composites is 2 orders of magnitude higher than that of pristine polymer. Also, the POT-DBSA/Pd composite exhibits magnetic property. The formation mechanism of the POT-DBSA/Au or Pd composite nanosphere is discussed.
Publisher: Wiley
Date: 23-08-2006
DOI: 10.1002/PAT.735
Publisher: Royal Society of Chemistry (RSC)
Date: 2014
DOI: 10.1039/C3TA13875E
Publisher: Elsevier BV
Date: 10-2007
Publisher: American Scientific Publishers
Date: 08-2010
Publisher: Elsevier BV
Date: 05-2008
Publisher: Elsevier BV
Date: 10-2014
Publisher: Elsevier BV
Date: 05-2016
DOI: 10.1016/J.BIOS.2015.12.054
Abstract: In this report, titanium nitride (TiN) nanoparticles decorated multi-walled carbon nanotube (MWCNTs) nanocomposite is fabricated via a two-step process. These two steps involve the decoration of titanium dioxide nanoparticles onto the MWCNTs surface and a subsequent thermal nitridation. Transmission electron microscopy shows that TiN nanoparticles with a mean diameter of ≤ 20 nm are homogeneously dispersed onto the MWCNTs surface. Direct electrochemistry and electrocatalysis of cytochrome c immobilized on the MWCNTs-TiN composite modified on a glassy carbon electrode for nitrite sensing are investigated. Under optimum conditions, the current response is linear to its concentration from 1 µM to 2000 µM with a sensitivity of 121.5 µA µM(-1)cm(-2) and a low detection limit of 0.0014 µM. The proposed electrode shows good reproducibility and long-term stability. The applicability of the as-prepared biosensor is validated by the successful detection of nitrite in tap and sea water s les.
Publisher: MDPI AG
Date: 15-03-2021
Abstract: The introduction of toxic chemicals into the environment can result in water pollution leading to the degradation of bio ersity as well as human health. This study presents a new approach of using metal oxides (Al2O3 and SiO2) modified with a plasmonic metal (silver, Ag) nanoparticles (NPs)-based nanofluid (NF) formulation for environmental remediation purposes. Firstly, we prepared the Al2O3 and SiO2 NFs of different concentrations (0.2 to 2.0 weight %) by ultrasonic-assisted dispersion of Al2O3 and SiO2 NPs with water as the base fluid. The thermo-physical (viscosity, activation energy, and thermal conductivity), electrical (AC conductivity and dielectric constant) and physical (ultrasonic velocity, density, refractive index) and stability characteristics were comparatively evaluated. The Al2O3 and SiO2 NPs were then catalytically activated by loading silver NPs to obtain Al2O3/SiO2@Ag composite NPs. The catalytic reduction of 4-nitrophenol (4-NP) with Al2O3/SiO2@Ag based NFs was followed. The catalytic efficiency of Al2O3@Ag NF and SiO2@Ag NF, for the 4-NP catalysis, is compared. Based on the catalytic rate constant evaluation, the catalytic reduction efficiency for 4-NP is found to be superior for 2% weight Al2O3@Ag NF (92.9 × 10−3 s−1) as compared to the SiO2@Ag NF (29.3 × 10−3 s−1). Importantly, the enhanced catalytic efficiency of 2% weight Al2O3@Ag NF for 4-NP removal is much higher than other metal NPs based catalysts reported in the literature, signifying the importance of NF formulation-based catalysis.
Publisher: Elsevier BV
Date: 03-2013
Publisher: Elsevier BV
Date: 06-2016
Publisher: MDPI AG
Date: 26-12-2019
Abstract: Copper oxide (CuO) and cerium oxide (CeO2) of various concentrations have been prepared through an ultrasonically assisted dispersion of CuO and CeO2 nanoparticles (NPs) in which water and nanofluids (NFs) were formulated. The morphological properties of the CuO and CeO2 NPs are reported. Few of the physicochemical properties that can influence the photocatalytic activities of the NFs are evaluated, such as viscosity, activation energy, density, thermal conductivity, electrical conductivity, alternating current (AC) conductivity, pH, stability, refractive index and optical band gap of the CuO and CeO2 NFs. Viscosity studies have been made at four different temperatures (303 K, 308 K, 313 K and 318 K) and the activation energy is calculated and compared between the CuO and CeO2 NFs. The thermal conductivity of the two NFs is calculated and compared. Electrical conductivity is measured for CuO and CeO2 NFs using an impedance analyzer at different frequencies at 303 K. The dielectric constant and AC conductivity were studied. The electrical conductivity and pH of the prepared NFs are measured and the results are compared. The stability of the NFs is determined from Zeta potential values obtained from dynamic light scattering measurements. UV-Visible diffuse reflectance measurements were used to deduce the optical bandgap of the respective metal oxide NPs in the NFs. The photocatalytic efficiencies of the CuO NFs and CeO2 NFs were evaluated using methylene blue (MB) as the model dye. The rate constant for the photodegradation of MB was higher for CuO NF as compared CeO2 NF and also higher than simple NPs-based photocatalysts. A plausible explanation for the role of NFs over the simple NPs-based photocatalytic solution is presented.
Publisher: Royal Society of Chemistry (RSC)
Date: 2013
DOI: 10.1039/C3JA30300D
Publisher: MDPI AG
Date: 11-02-2019
DOI: 10.3390/CATAL9020170
Abstract: The quest for developing highly efficient TiO2-based photocatalysts is continuing and, in particular, evolving a new strategy is an important aspect in this regard. In general, much effort has been devoted to the anatase TiO2 modifications, despite there being only a few recent studies on rutile TiO2 (rTiO2). To the best of our knowledge, studies on the preparation and characterization of the photocatalysts based on the intentional inclusion of graphene (G) into rTiO2 nanostructures have not been reported yet. Herein, we develop a new type of TiO2-based photocatalyst comprising of G included pure rTiO2 nanowire (abbreviated as rTiO2(G) NW) with enhanced visible light absorption capability. To prepare rTiO2(G) NW, the G incorporated titanate electrospun fibers were obtained by electrospinning and subsequently heat treated at various temperatures (500 to 800 °C). Electrospinning conditions were optimized for producing good quality rTiO2(G) NW. The rTiO2(G) NW and their corresponding s les were characterized by appropriate techniques such as X-ray diffraction (XRD), scanning electron microscopy, high-resolution transmission electron microscopy and UV-vis diffuse reflectance spectroscopy to ascertain their material characteristics. XRD results show that the lattice strain occurs upon inclusion of G. We present here the first observation of an apparent bandgap lowering because of the G inclusion into TiO2 NW. While anatase TiO2 NW exhibited poor visible light photocatalysis towards NOx removal, the rTiO2(G) NW photocatalyst witnessed a significantly enhanced (~67%) photocatalytic performance as compared to anatase TiO2(G) NW. We concluded that the inclusion of G into rTiO2 nanostructures enhances the visible light photoactivity. A plausible mechanism for photocatalysis is suggested.
Publisher: Elsevier BV
Date: 04-2008
Publisher: MDPI AG
Date: 26-01-2018
Publisher: MDPI AG
Date: 09-02-2021
DOI: 10.3390/NANO11020440
Abstract: Magnetic nanoparticles (MNPs) are widely used materials for biomedical applications owing to their intriguing chemical, biological and magnetic properties. The evolution of MNP based biomedical applications (such as hyperthermia treatment and drug delivery) could be advanced using magnetic nanofluids (MNFs) designed with a biocompatible surface coating strategy. This study presents the first report on the drug loading/release capability of MNF formulated with methoxy polyethylene glycol (referred to as PEG) coated MNP in aqueous (phosphate buffer) fluid. We have selected MNPs (NiFe2O4, CoFe2O4 and Fe3O4) coated with PEG for MNF formulation and evaluated the loading/release efficacy of doxorubicin (DOX), an anticancer drug. We have presented in detail the drug loading capacity and the time-dependent cumulative drug release of DOX from PEG-coated MNPs based MNFs. Specifically, we have selected three different MNPs (NiFe2O4, CoFe2O4 and Fe3O4) coated with PEG for the MNFs and compared their variance in the loading/release efficacy of DOX, through experimental results fitting into mathematical models. DOX loading takes the order in the MNFs as CoFe2O4 NiFe2O4 Fe3O4. Various drug release models were suggested and evaluated for the in idual MNP based NFs. While the non-Fickian diffusion (anomalous) model fits for DOX release from PEG coated CoFe2O4, PEG coated NiFe2O4 NF follows zero-order kinetics with a slow drug release rate of 1.33% of DOX per minute. On the other hand, PEG coated NiFe2O4 follows zero-order DOX release. Besides, several thermophysical properties and magnetic susceptibility of the MNFs of different concentrations have been studied by dispersing the MNPs (NiFe2O4, CoFe2O4 and Fe3O4) in the base fluid at 300 K under ultrasonication. This report on the DOX loading/release capability of MNF will set a new paradigm in view that MNF can resolve problems related to the self-heating of drug carriers during mild laser treatment with its thermal conducting properties.
Publisher: American Scientific Publishers
Date: 04-2014
Abstract: Herein, we report an attractive, simple and templateless synthetic method for the formation of anisotropic gold nanostructures. Gold 'mesoflowers' consisting of arrays of nanoplatelets were synthesized by electrochemical gold deposition on/off conditions onto a conducting poly(diphenylamine) (PDPA) support matrix. A possible forming mechanism of anisotropic gold nanostructures is presented. The electronic and electrochemical properties of gold nanoflower decorated PDPA in an assembled diode configuration were evaluated.
Publisher: MDPI AG
Date: 25-10-2019
DOI: 10.3390/CATAL9110888
Abstract: In this study, the fabrication of a metal oxide nanoparticles (NPs) dispersed catalytic electrode is described based on a new alternating current (AC) plasma deposition approach. The fabrication involves the treatment of AC plasma on a precursor solution comprised of metal salts such as CuCl2, FeCl2, and ZnCl2, and a monomer (acrylic acid) in the presence/absence of a cross-linker. Furthermore, the utility of such developed electrodes has been demonstrated for the electrochemical determination of hydrogen peroxide (H2O2). The electrode materials obtained through plasma treatment was characterized by Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscope (SEM), contact angle measurements, energy-dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), and cyclic voltammetry. Among the metal oxide modified electrodes prepared by the AC plasma deposition method, the copper oxide (CuO) NPs catalytic electrode exhibited significant oxidation and reduction peaks for H2O2 in phosphate-buffered saline solution. The catalytic electrode with CuO NPs exhibited a combination of good H2O2 sensing characteristics such as good sensitivity (63.52 mA M−1 cm−2), good selectivity, low detection limits (0.6 µM), fast sensing response (5 s), a wide linear range (0.5–8.5 mM), and good stability over 120 cycles. Based on our results, it is well demonstrated that plasma deposition could be effectively utilized for the fabrication of the catalytic electrode for detection of H2O2 concentrations. Further, the strategy of using AC plasma for fabrication of metal oxide-based modified electrodes could also be extended for the fabrication of other kinds of nanomaterials-based sensors.
Publisher: Elsevier BV
Date: 10-2015
Location: United States of America
No related grants have been discovered for Gopalan Anantha Iyengar.