The Role of Acid Concentration on Band Gap Shrinkage in Cellulose Nanocrystals Fabricated from Water Hyacinth

In this study, the fingerprint of the acid concentration during the hydrolysis process on the optical band gap of cellulose nanocrystals (CNCs) has been systematically studied. The CNCs have been prepared using hydrochloric acid at a hydrolysis temperature of 50°C and at a constant hydrolysis time of 4 hours but with varying hydrochloric cid concentrations of 5%, 10% and 15%. The crystalline structure and phase identification of the CNCs have been studied using XRD technique. UV-Vis Spectroscopy has been done and the optical band gap energy calculated by performing the Tauc’s plot. From the study, the grain size has been found to decrease with acid concentration while the band gap energy has been found to increase with increasing acid concentration. Further, the optical band gaps of the CNCs have been found to decrease with the increase in crystallite size. This shrinkage of the band gap has been attributed to the increased impurity concentration leading to the narrowing of the band gap due to the emerging of the impurity band formed by the overlapped impurity states

Enhancing the Optical Properties of Chitosan, Carboxymethyl Cellulose, Sodium Alginate Modified with Nano Metal Oxide and Graphene Oxide

The solution casting method was utilized to synthesize nanocomposite films of chitosan (Cs)/CuO, Cs/graphene oxide (GO), carboxymethyl cellulose (CMC)/TiO2, CMC/GO, sodium alginate (Na Alg)/TiO2, and Na-Alg/GO owing to their various applications. The influence of CuO, TiO2 and GO concentration on the optical properties of Cs, CMC and Na-Alg films was studied by UV-Vis Spectroscopy. The absorbance of Cs, CMC and Na-Alg increased with increasing the filler content, thus reflecting the dependence of Cs, CMC, and Na-Alg properties on the nanofiller content, and confirming the interactions between individual polymers and CuO, TiO2 and GO nanoparticles. The obtained absorbance values were then used to calculate the absorption coefficient and, hence, the optical band gap values. The characteristic absorption bands of CuO and TiO2 underwent a redshift by increasing the filler content. The results showed that the optical band gap of Cs, CMC, and Na-Alg decreased with filler content, and they possessed 1, 2 and 2 band gaps respectively. The obtained results recommended that Cs, CMC, and Na-Alg nanocomposites can be used in optoelectronic devices.

Influence of Nano Filler (ZrO2) on Optical and Thermal Studies of Potassium Doped Polyethylene Oxide Solid Polymer Electrolytes

Solid polymer electrolyte films made with potassium doped Polyethylene oxide using ZrO2 as nanofiller (70PEO-30KBF4-x ZrO2 where x = 1, 2.5, 5, 7.5, & 10 wt% ­­) were prepared by solution casting technique. Optical and thermal properties of polymer electrolyte films were studied by using Optical absorption and DSC techniques. From Optical absorption spectra, it is observed that fundamental absorption edge is shifted towards the higher wavelength side (range 259- 297 nm) with increase of nano filler (ZrO­2) concentration (1-10 wt %). Optical band gap for all electronic transitions (p=1/2, 2, 2/3 and 1/3) are found to be increased as incorporation of nano filler (ZrO2) which confirms the structural rearrangements takes place in polymer electrolyte films. Optical band gap for indirect allowed transitions (p=1/2) are found to be in the range of 1.93-3.34eV. Decrease in Urbach energy (4.8eV- 1.4eV) is associated with decrease in defect formation in host polymeric matrix (PEO-KBF4) as a result of embedded nano filler (ZrO2). DSC spectra analysis of polymer electrolytes has showed melting temperatures in the range 63.63-73.71°C and highest crystallinity is found to be 85 % (10 wt % ZrO­2). Enthalpy values are elevated with increase in nanofiller composition (ZrO2) in the present polymer electrolyte films.Keywords: PEO based polymer electrolytes, Solid polymer electrolytes, Optical and Thermal studies.

Structure and photophysics of rubrene-tetracene blends

The application potential of singlet fission (SF), describing the spontaneous conversion of an excited singlet into two triplets, underlines the necessity to independently control SF rates, energetics and the optical band gap. Heterofission, whereby the singlet splits into triplets on chemically distinct chromophores, is a promising approach to control the above-mentioned parameters, but its details are not yet fully understood. Here, we investigate the photophysics of blends of two prototypical SF chromophores, tetracene (TET) and rubrene (RUB) using time-resolved photoluminescence spectroscopy and time-correlated single photon counting (TCSPC) to explore the potential for heterofission in combinations of endothermic SF chromophores.