Eranezhuth Wasan Awin

Bio: Eranezhuth Wasan Awin is an academic researcher from Indian Institute of Technology Madras. The author has contributed to research in topics: Nanocomposite & Ceramic. The author has an hindex of 5, co-authored 12 publications receiving 96 citations.

Dominating role of crystal structure over defect chemistry in black and white zirconia on visible light photocatalytic activity.

Abstract: Nanometric powder particles of white zirconia were synthesized through precursor route by the pyrolysis of zirconium (IV) butoxide at varied temperatures in air ranging from 900–1400 °C and were predominantly monoclinic in nature. To control the defect chemistry, the precursor was also pyrolyzed in a reduced atmosphere at 900 °C, eventually resulting in black zirconia. The stabilization of tetragonal phase and observed color change from white to black in samples pyrolyzed under reduced atmosphere was attributed to the creation of oxygen vacancies and disorder. The black and white zirconia produced delineated the influence of crystal structure and oxygen vacancies on the photocatalytic performance. Furthermore, zirconia synthesized at lower temperatures (600 and 800 °C) in air confirmed the detrimental role of tetragonal phase on the degradation behavior of methylene blue dye. High photocatalytic degradation rate for white zirconia was attributed to the presence of increased density of nano-sized pores and low recombination rate of electron-hole pairs as confirmed by PL measurements. Interestingly, black zirconia exemplified relatively limited activity albeit presence of oxygen vacancies. This negative effect was attributed to the presence of tetragonal phase and possibly, the insufficient creation of new energy states near valence and conduction band towards Fermi energy level.

Novel Precursor-Derived Meso-/Macroporous TiO2/SiOC Nanocomposites with Highly Stable Anatase Nanophase Providing Visible Light Photocatalytic Activity and Superior Adsorption of Organic Dyes

Abstract: Titania (TiO₂) is considered to have immense potential as a photocatalyst, the anatase phase in particular. There have been numerous attempts to push the limits of its catalytic activity to higher wavelengths to harness the visible electromagnetic radiation. Most of the investigations till date have been restricted to fine-tuning the bandgap by doping, control of defect chemistry at the surface and several to first principle simulations either with limited success or success at the cost of complexities in processing. Here, we report a simple and elegant way of preparing ceramics through precursor chemistry which involves synthesis of macroporous and mesoporous nanocomposites with in situ formation of TiO₂ nanocrystals into a robust and protecting SiOC matrix. The in situ nanoscaled TiO₂ is anatase of size 9-10 nm, which is uniformly distributed in an amorphous SiOC matrix forming a new generation of nanocomposites that combine the robustness, structural stability and durability of the SiOC matrix while achieving nanoscaled TiO₂ functionalities. The stabilization of the anatase phase even at temperature as high as 1200 °C was evident. With an average pore size of 6.8 nm, surface area of 129 m²/g (BET) and pore volume of 0.22 cm³/g (BET), mesoporosity was achieved in the nanocomposites. The composites exhibited visible light photocatalytic activity, which is attributed to the Ti-O-C/TiC bonds resulting in the reduction of band gap by 0.2 to 0.9 eV. Furthermore, the heterojunction formed between the amorphous SiOC and crystalline TiO₂ is also expected to minimize the recombination rate of electron-hole pair, making these novel nanocomposites based on TiO₂ extremely active in visible wavelength regime.

Design of nanoscaled heterojunctions in precursor-derived t-ZrO2/SiOC(N) nanocomposites: Transgressing the boundaries of catalytic activity from UV to visible light.

Abstract: In this work, nanocomposites made of nanosized zirconia crystallized in situ in an amorphous silicon oxycarbo(nitride) (SiOC(N)) matrix have been designed through a precursor route for visible light photocatalytic applications. The relative volume fraction of the starting precursors and the pyrolysis temperatures not only influences the phase fraction of zirconia crystallites but also stabilizes the tetragonal crystal structure of zirconia (t-ZrO2) at room temperature. The presence of carbon in interstitial sites of zirconia and oxygen vacancy defects led to drastic reduction in the band gap (2.2 eV) of the nanocomposite. Apart from being a perfect host avoiding sintering of the active phase and providing mechanical stability, the amorphous matrix also reduces the recombination rate by forming heterojunctions with t-ZrO2. The reduction in band gap as well as the formation of heterojunctions aids in harnessing the visible light for photocatalytic activity.

Photocatalytic hydrogen production using metal doped TiO2: A review of recent advances

Abstract: Hydrogen (H2) production via photocatalytic water splitting is one of the most promising technologies for clean solar energy conversion to emerge in recent decades. The achievement of energy production from water splitting would mean that we could use water as a fuel for future energy need. Among the various photocatalytic materials, titanium dioxide (TiO2) is the dominant and most widely studied because of its exceptional physico-chemical characteristics. Surface decoration of metal/non-metal on TiO2 nanoparticles is an outstanding technique to revamp its electronic properties and enrich the H2 production efficiency. Metal dopants play a vital role in separation of electron-hole pairs on the TiO2 surface during UV/visible/simulated solar light irradiation. In this paper, the basic principles, photocatalytic-reactor design, kinetics, key findings, and the mechanism of metal-doped TiO2 are comprehensively reviewed. We found that Langmuir-Hinshelwood kinetic model is commonly employed by the researchers to demonstrate the rate of H2 production. Copper (Cu), gold (Au) and platinum (Pt) are the most widely studied dopants for TiO2, owing to their superior work function. The metal dopants can amplify the H2 production efficiency of TiO2 through Schottky barrier formation, surface plasmon resonance (SPR), generation of gap states by interaction with TiO2 VB states. The recent advances and important consequences of 2D materials, perovskites, and other novel photocatalysts for H2 generation have also been reviewed.

Structure and oxygen mobility in mayenite (Ca12Al14O33): a high-temperature neutron powder diffraction study Locality: synthetic Sample: T = 1223 K

Abstract: The structure of mayenite, Ca(12)Al(14)O(33), was investigated by neutron powder diffraction up to 1323 K. It has been described previously as a calcium-aluminate framework, in which 32 of the 33 oxygen anions are tightly bound, containing large cages, 1/6 of them being filled randomly by the remaining 'free' oxygen. At ambient temperature excess oxygen was found, corresponding to the composition Ca(12)Al(14)O(33.5) which was attributed to the presence of hydroxide, peroxide and superoxide radicals in the cages. Above 973 K these are lost under vacuum conditions and the composition becomes stoichiometric. From the refined structural parameters it is concluded that the structure is more adequately described as a relatively stable aluminate framework consisting of eightfold rings of AlO(4) tetrahedra with disordered Ca and 'free' O distributed within. At high temperatures the density of the 'free' oxygen is extremely spread out, with the expansion being related to the high ionic conductivity of this material. Since no continuous density distribution between adjacent cages was found and the 'free' O forms bonds with part of the Ca, the diffusion proceeds via a jump-like process involving exchange of the 'free' oxygen with framework oxygen. The results confirm the recent theoretical predictions of Sushko et al.

Influence of parameters on the heterogeneous photocatalytic degradation of pesticides and phenolic contaminants in wastewater : a short review

Abstract: In recent years, the application of heterogeneous photocatalytic water purification process has gained wide attention due to its effectiveness in degrading and mineralizing the recalcitrant organic compounds as well as the possibility of utilizing the solar UV and visible light spectrum. This paper aims to review and summarize the recently published works on the titanium dioxide (TiO2) photocatalytic oxidation of pesticides and phenolic compounds, predominant in storm and waste water effluents. The effect of various operating parameters on the photocatalytic degradation of pesticides and phenols are discussed. Results reported here suggested that the photocatalytic degradation of organic compounds depends on the type of photocatalyst and composition, light intensity, initial substrate concentration, amount of catalyst, pH of the reaction medium, ionic components in water, solvent types, oxidizing agents/electron acceptors, catalyst application mode, and calcinations temperature in water environment. A substantial amount of research has focused on the enhancement of TiO2 photocatalysis by modification with metal, non-metal and ion doping. Recent developments in TiO2 photocatalysis for the degradation of various pesticides and phenols are also highlighted in this review. It is evident from the literature survey that photocatalysis has shown good potential for the removal of various organic pollutants. However, still there is a need to find out the practical utility of this technique on commercial scale.