Debraj Gangopadhyay

Bio: Debraj Gangopadhyay is an academic researcher from University of Lucknow. The author has contributed to research in topics: Raman spectroscopy & Hydrogen bond. The author has an hindex of 8, co-authored 23 publications receiving 145 citations. Previous affiliations of Debraj Gangopadhyay include Banaras Hindu University & Academy of Sciences of the Czech Republic.

In vitro concentration dependent detection of creatinine: a surface enhanced Raman scattering and fluorescence study

Abstract: An attempt has been made to detect the concentration of creatinine in a very dilute aqueous solution in vitro on the basis of the Jaffe reaction, the commonly used reaction for clinical determination of creatinine concentration in blood serum or urine. For this various spectroscopic techniques viz. Raman spectroscopy, surface enhanced Raman scattering, UV-visible and fluorescence spectroscopy have been used. As a result of the Jaffe reaction using aqueous solutions of creatinine at different concentrations and picric acid and NaOH as reagents, a reddish orange colored Jaffe complex is produced. The concentration dependent SERS spectra of the Jaffe complex show gradual decrease in the intensity of ring deformation mode of creatinine on decreasing creatinine concentration. The concentration dependent absorption spectra of the Jaffe complex show changes in intensity in one of the absorption peaks characteristic of creatinine. The concentration dependent fluorescence emission spectra of the Jaffe complex show a blue shift in emission maxima on reducing the concentration of creatinine in the solution. The observed results suggest the possibility to detect the concentration of creatinine in a very dilute solution in vitro by SERS and fluorescence techniques and the application of these techniques in vivo might aid in a more specific and accurate determination of creatinine in serum or urine.

Low-Temperature In Situ Amino Functionalization of TiO2 Nanoparticles Sharpens Electron Management Achieving over 21% Efficient Planar Perovskite Solar Cells.

Abstract: Titanium oxide (TiO2 ) has been commonly used as an electron transport layer (ETL) of regular-structure perovskite solar cells (PSCs), and so far the reported PSC devices with power conversion efficiencies (PCEs) over 21% are mostly based on mesoporous structures containing an indispensable mesoporous TiO2 layer. However, a high temperature annealing (over 450 °C) treatment is mandatory, which is incompatible with low-cost fabrication and flexible devices. Herein, a facile one-step, low-temperature, nonhydrolytic approach to in situ synthesizing amino-functionalized TiO2 nanoparticles (abbreviated as NH2 -TiO2 NPs) is developed by chemical bonding of amino (-NH2 ) groups, via TiN bonds, onto the surface of TiO2 NPs. NH2 -TiO2 NPs are then incorporated as an efficient ETL in n-i-p planar heterojunction (PHJ) PSCs, affording PCE over 21%. Cs0.05 FA0.83 MA0.12 PbI2.55 Br0.45 (abbreviated as CsFAMA) PHJ PSC devices based on NH2 -TiO2 ETL exhibit the best PCE of 21.33%, which is significantly higher than that of the devices based on the pristine TiO2 ETL (19.82%) and is close to the record PCE for devices with similar structures and fabrication procedures. Besides, due to the passivation of the surface trap states of perovskite film, the hysteresis of current-voltage response is significantly suppressed, and the ambient stability of devices is improved upon amino functionalization.

Phase Transition Enthalpy Measurements of Organic and Organometallic Compounds and Ionic Liquids. Sublimation, Vaporization, and Fusion Enthalpies from 1880 to 2015. Part 2. C11–C192

Abstract: The second part of this compendium concludes with a collection of phase change enthalpies of organic molecules inclusive of C11–C192 reported over the period 1880–2015. Also included are phase change enthalpies including fusion, vaporization, and sublimation enthalpies for organometallic, ionic liquids, and a few inorganic compounds. Paper I of this compendium, published separately, includes organic compounds from C1 to C10 and describes a group additivity method for evaluating solid, liquid, and gas phase heat capacities as well as temperature adjustments of phase changes. Paper II of this compendium also includes an updated version of a group additivity method for evaluating total phase change entropies which together with the fusion temperature can be useful in estimating total phase change enthalpies. Other uses include application in identifying potential substances that either form liquid or plastic crystals or exhibit additional phase changes such as undetected solid–solid transitions or behave ani...

A hybrid LIBS–Raman system combined with chemometrics: an efficient tool for plastic identification and sorting

Abstract: Classification of plastics is of great importance in the recycling industry as the littering of plastic wastes increases day by day as a result of its extensive use. In this paper, we demonstrate the efficacy of a combined laser-induced breakdown spectroscopy (LIBS)–Raman system for the rapid identification and classification of post-consumer plastics. The atomic information and molecular information of polyethylene terephthalate, polyethylene, polypropylene, and polystyrene were studied using plasma emission spectra and scattered signal obtained in the LIBS and Raman technique, respectively. The collected spectral features of the samples were analyzed using statistical tools (principal component analysis, Mahalanobis distance) to categorize the plastics. The analyses of the data clearly show that elemental information and molecular information obtained from these techniques are efficient for classification of plastics. In addition, the molecular information collected via Raman spectroscopy exhibits clearly distinct features for the transparent plastics (100% discrimination), whereas the LIBS technique shows better spectral feature differences for the colored samples. The study shows that the information obtained from these complementary techniques allows the complete classification of the plastic samples, irrespective of the color or additives. This work further throws some light on the fact that the potential limitations of any of these techniques for sample identification can be overcome by the complementarity of these two techniques.