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541.
Mukhtar Ahmad R. Grössinger M. Kriegisch F. Kubel M.U. Rana 《Current Applied Physics》2012,12(6):1413-1420
A series of Al-substituted Co2W hexaferrites BaCo2AlxFe16 ? xO27 (x = 0, 0.2, 0.4, 0.6, 0.8, 1) synthesized by sol-gel autocombustion method have been investigated. The samples were characterized by DTA/TGA analysis, FTIR spectroscopy, X-ray Diffractometer and field emission gun scanning electron microscopy (FEGSEM). Magnetic behavior of a selected sample was examined up to a magnetic field of 9T between a temperature range of 4.2 K–400 K. The values of saturation magnetization were calculated by the law of approach to saturation. The coercivity of the investigated sample has a value of about hundred oersteds at room temperature which is favorable for EM materials. The complex permittivity and complex permeability of a composite sample have been measured in the frequency range of 0.5–13 GHz. Based on the theoretical calculation of re?ection loss; the microwave absorption properties have been investigated. The results indicate that the attenuation peak frequency of these compounds can be tuned for the desired frequency by varying the thickness of the absorber. 相似文献
542.
Dr. Yang Yu Le Wang Dr. Dongqing Lin Dr. Shammi Rana Dr. Kunal S. Mali Prof. Haifeng Ling Prof. Linghai Xie Prof. Steven De Feyter Dr. Junzhi Liu 《Angewandte Chemie (International ed. in English)》2023,62(22):e202303335
Two wide-band gap U-shaped polycyclic aromatic hydrocarbons with/without boron and nitrogen (BN-) doping ( BN-1 and C-1 ) were synthesized to tune the electronic features to suit the performance requirements for organic field-effect transistor memory (OFET-NVM). The chemical structures were characterized by scanning tunneling microscopy and single-crystal diffraction. Owing to the electron-donor effect of N and the high electron affinity of B, the BN-1 -based OFET-NVM displays large ambipolar memory windows and an enhanced charge storage density compared to C-1 and most reported small molecules. A novel supramolecular system formed from BN-1 and PMMA contributes to fabricating uniform films with homogeneous microstructures, which serve as a two-in-one tunnelling dielectric and charge-trapping layer to realize long-term charge retention and reliable endurance. Our results demonstrate that both BN doping and supramolecular engineering are crucial for the charge trapping of OFET-NVM. 相似文献
543.
Bhawna Kaushik Pooja Rana Deepti Rawat Kanika Solanki Pooja Rana Shallu Sachdeva Dhanaji R. Naikwadi Ankush V. Biradar Rakesh K. Sharma 《应用有机金属化学》2023,37(1):e6936
Construction of an effective heterojunction for unimpeded flow of photogenerated charges and their prolonged separation is imperative for environmental photocatalysis. Herein, we have designed an efficient magnetic ZnO/BiVO4 type-II heterostructure, which was employed for proficient degradation of persistent methyl violet dye with an efficiency of 97.6% in 90 min and a hazardous organic pollutant, namely, bisphenol A. UV-DRS and photoluminescence studies demonstrated that the fabricated nanocomposite exhibited effective light absorption and prolonged charge separation, thereby resulting in high photocatalytic efficacy under visible light irradiation. The efficacy of developed magnetic ZnO/BiVO4 was also compared with pristine BiVO4 and undoped magnetic ZnO, which indicated that the constructed heterostructure displayed approximately threefold and sixfold activity in contrast with bare BiVO4 and undoped magnetic ZnO nanoparticles, respectively. Radical trapping studies, ESR analysis along with GC-MS analysis were conducted to elucidate the mechanistic pathway during the photodegradation process. This work provides a rational technical approach and research ideas for photocatalytic degradation of harmful organic pollutants in an environment-friendly manner by employing energy-efficient LEDs. Besides, good recyclability of catalyst makes it a promising candidate for large-scale applications. 相似文献
544.
Dibya Prakash Biswal Dipankar Singha Dr. Jagannath Panda Dr. Malay Kumar Rana 《Chemphyschem》2023,24(21):e202300311
UiO-66-NH2-IM, a fluorescent metal-organic framework (MOF), was synthesized by post-synthetic modification of UiO-66-NH2 with 2-imidazole carboxaldehyde via a Schiff base reaction. It was examined using various characterization techniques (PXRD, FTIR, NMR, SEM, TGA, UV-Vis DRS, and photoluminescence spectroscopy). The emissive feature of UiO-66-NH2-IM was utilized to detect volatile organic compounds (VOCs), metal ions, and anions, such as acetone, Fe3+, and carbonate (CO32−). Acetone turns off the high luminescence of UiO-66-NH2-IM in DMSO, with the limit of detection (LOD) being 3.6 ppm. Similarly, Fe3+ in an aqueous medium is detected at LOD=0.67 μM (0.04 ppm) via quenching. On the contrary, CO32− in an aqueous medium significantly enhances the luminescence of UiO-66-NH2-IM, which is detected with extremely high sensitivity (LOD=1.16 μM, i. e., 0.07 ppm). Large Stern-Volmer constant, Ksv, and low LOD values indicate excellent sensitivity of the post-synthetic MOF. Experimental data supported by density functional theory (DFT) calculations discern photo-induced electron transfer (PET), resonance energy transfer (RET), inner filter effect (IFE), or proton abstraction as putative sensing mechanisms. NMR and computational studies propose a proton abstraction mechanism for luminescence enhancement with CO32−. Moreover, the optical behavior of the post-synthetic material toward analytes is recyclable. 相似文献
545.
Dr. Andreas Hermann Rana Seymen Dr. Lukas Brieger Johannes Kleinheider Dr. Bastian Grabe Prof. Dr. Wolf Hiller Prof. Dr. Carsten Strohmann 《Angewandte Chemie (International ed. in English)》2023,62(25):e202302489
Since its introduction in 2004, Knochel's so called Turbo-Grignard reagents revolutionized the usage of Grignard reagents. Through the simple addition of LiCl to a magnesium alkyl an outstanding increase in reactivity can be achieved. Though the exact composition of the reactive species remained mysterious, the reactive mixture itself is readily used not only in synthesis but also found its way into more distant fields like material science. To unravel this mystery, we combined single-crystal X-ray diffraction with in-solution NMR-spectroscopy and closed our investigations with quantum chemical calculations. Using such a variety of methods, we have gained insight into and an explanation for the extraordinary reactivity of this extremely convenient reagent by determining the structure of the first bimetallic reactive species [t-Bu2Mg ⋅ LiCl ⋅ 4 thf] with two tert-butyl anions at the magnesium center and incorporated lithium chloride. 相似文献
546.
Dr. Supriya Ghosh Dr. Debkumar Rana Dr. Bapi Pradhan Dr. Patrice Donfack Prof. Dr. Johan Hofkens Prof. Dr. Dr. Arnulf Materny 《Chemphyschem》2023,24(21):e202300303
In recent years, there has been an impressively fast technological progress in the development of highly efficient lead halide perovskite solar cells. Nonetheless, the stability of perovskite films and associated solar cells remains a source of uncertainty and necessitates sophisticated characterization techniques. Here, we report low- to mid-frequency resonant Raman spectra of formamidinium-based lead mixed-halide perovskites. The assignment of the different Raman lines in the measured spectra is assisted by DFT simulations of the Raman spectra of suitable periodic model systems. An important result of this work is that both experiment and theory point to an increase of the stability of the perovskite structure with increasing chloride doping concentration. In the Raman spectra, this is reflected by the appearance of new lines due to the formation of hydrogen bonds. Thus, higher chloride doping results in less torsional motion and lower asymmetric bending contributing to higher stability. This study yields a solid basis for the interpretation of the Raman spectra of formamidinium-based mixed-halide perovskites, furthering the understanding of the properties of these materials, which is essential for their full exploitation in solar cells. 相似文献