Jitender Jindal

Bio: Jitender Jindal is an academic researcher from Maharshi Dayanand University. The author has contributed to research in topics: Luminescence & Anodizing. The author has an hindex of 6, co-authored 19 publications receiving 156 citations.

S-, N- and C-doped ZnO as semiconductor photocatalysts: A review

Abstract: In the past few decades, many novel non-metal doped ZnO materials have developed hasty interest due to their adaptable properties such as low recombination rate and high activity under the solar light exposure. In this article, we compiled recent research advances in non-metal (S, N, C) doped ZnO, emphasizing on the related mechanism of catalysis and the effect of non-metals on structural, morphological, optical and photocatalytic characteristics of ZnO. This review will enhance the knowledge about the advancement in ZnO and will help in synthesizing new ZnO-based materials with modified structural and photocatalytic properties.

Synthesis and Charcterization of Coupled ZnO/SnO2 Photocatalysts and Their Activity towards Degradation of Cibacron Red Dye

Abstract: A series of coupled ZnO-SnO2 photocatalyst was successfully synthesized in the Zn:Sn molar ratio of 20:1, 10:1, 5:1 and 2:1 via co-precipitation method followed by calcination at different temperatures. The synthesized materials were characterized by X-ray diffraction, diffuse reflectance spectra, scanning electron microscope and transmission electron microscope. Photocatalytic activitiy of synthesized materials was applied for the degradation of cibacron red dye in aqueous solution under UV-A light irradiation. Experimental results revealed that the coupled ZnO-SnO2 photocatalyst with Zn:Sn molar ratio 10:1, calcined at 600oC for 1 h was the most efficient photocatalyst among synthesized samples for the degradation of cibacron red. Superoxide anion radical (•O2–) was found to be the prominent active species responsible for degradation comparative to hole (h+), hydroxyl radical (•OH).

Carbon materials as CO2 adsorbents: a review

Abstract: Environmental pollution is a serious issue with the rapid development of urbanization, industrialization and vehicle traffic. In particular, fossil fuel pollution increases atmospheric CO2 levels. To alleviate this problem, various carbon capture and storage technologies have been developed, yet they are actually limited by cost and energy requirements. Alternatively, adsorption appears as a promising technique for carbon capture due to its low cost, low energy requirement and applicability over a wide range of temperature and pressure. Here, we review carbonaceous materials such as activated carbon, activated carbon nanofibers, hollow carbon spheres and biochar for CO2 capture, and we discuss factors controlling CO2 adsorption. CO2 adsorption primarily depends upon micropore volume and surface area which in turn are controlled by carbonization and activation temperature, activating agent and its impregnation ratio, activation time and presence of moisture. Additionally, introduction of basic functional groups such as N-containing functional groups into the adsorbent enhances the adsorption capacities. We discuss possible modifications for cost-effective and commercially viable carbon materials as CO2 adsorbents.

Luminescence Properties of Eu2+/Eu3+ Activated Barium Aluminate Phosphors with Gd3+ Concentration Variation

Abstract: BaAl2O4:Eu2+/Eu3+ (1 mol %) co-doped with varying concentrations of Gd3+ (1, 2, 5 and 10 mol%) were prepared by combustion synthesis method at 600°C. All the compositions were investigated for their structural and photoluminescence properties. Samples prepared in open atmosphere showed the presence of both Eu3+ and Eu2+ states which indicates the reduction of Eu3+ to Eu2+ during the preparation of these compounds. The prepared materials at 600°C showed high intense broad peaks around 498 nm corresponding to Eu2+ and small peaks in the red region which are attributed to the presence of Eu3+. In the 1000°C annealed compounds, the intensity of the peak at 498 nm got increased. The intensity of this broad band for BaAl2O4:Eu2+/Eu3+(1 mol%):Gd3+(1 mol%) was three times than that of BaAl2O4:Eu2+/Eu3+(1 mol%). Thus second rare earth ion (Gd3+) acted as a good sensitizer and enhanced the photoluminescence intensity. The XRD spectra revealed the presence of hexagonal phase of BaAl2O4 as main phase and a small amou...

A Review of Microwave Synthesis of Zinc Oxide Nanomaterials: Reactants, Process Parameters and Morphologies

Abstract: Zinc oxide (ZnO) is a multifunctional material due to its exceptional physicochemical properties and broad usefulness. The special properties resulting from the reduction of the material size from the macro scale to the nano scale has made the application of ZnO nanomaterials (ZnO NMs) more popular in numerous consumer products. In recent years, particular attention has been drawn to the development of various methods of ZnO NMs synthesis, which above all meet the requirements of the green chemistry approach. The application of the microwave heating technology when obtaining ZnO NMs enables the development of new methods of syntheses, which are characterised by, among others, the possibility to control the properties, repeatability, reproducibility, short synthesis duration, low price, purity, and fulfilment of the eco-friendly approach criterion. The dynamic development of materials engineering is the reason why it is necessary to obtain ZnO NMs with strictly defined properties. The present review aims to discuss the state of the art regarding the microwave synthesis of undoped and doped ZnO NMs. The first part of the review presents the properties of ZnO and new applications of ZnO NMs. Subsequently, the properties of microwave heating are discussed and compared with conventional heating and areas of application are presented. The final part of the paper presents reactants, parameters of processes, and the morphology of products, with a division of the microwave synthesis of ZnO NMs into three primary groups, namely hydrothermal, solvothermal, and hybrid methods.

C-,N- and S-Doped TiO2 Photocatalysts: A Review

Abstract: This article presents an overview of the reports on the doping of TiO2 with carbon, nitrogen, and sulfur, including single, co-, and tri-doping. A comparison of the properties of the photocatalysts synthesized from various precursors of TiO2 and C, N, or S dopants is summarized. Selected methods of synthesis of the non-metal doped TiO2 are also described. Furthermore, the influence of the preparation conditions on the doping mode (interstitial or substitutional) with reference to various types of the modified TiO2 is summarized. The mechanisms of photocatalysis for the different modes of the non-metal doping are also discussed. Moreover, selected applications of the non-metal doped TiO2 photocatalysts are shown, including the removal of organic compounds from water/wastewater, air purification, production of hydrogen, lithium storage, inactivation of bacteria, or carbon dioxide reduction.

CO2 Capture at Medium to High Temperature Using Solid Oxide-Based Sorbents: Fundamental Aspects, Mechanistic Insights, and Recent Advances.

Abstract: Carbon dioxide capture and mitigation form a key part of the technological response to combat climate change and reduce CO2 emissions. Solid materials capable of reversibly absorbing CO2 have been the focus of intense research for the past two decades, with promising stability and low energy costs to implement and operate compared to the more widely used liquid amines. In this review, we explore the fundamental aspects underpinning solid CO2 sorbents based on alkali and alkaline earth metal oxides operating at medium to high temperature: how their structure, chemical composition, and morphology impact their performance and long-term use. Various optimization strategies are outlined to improve upon the most promising materials, and we combine recent advances across disparate scientific disciplines, including materials discovery, synthesis, and in situ characterization, to present a coherent understanding of the mechanisms of CO2 absorption both at surfaces and within solid materials.