School Of Basic And Applied Sciences

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    Effects of Dy3+-doping on the band-gap widening and formation of mixed cubic and monoclinic phases of Sm2O3 nanoparticles
    (Springer Science and Business Media Deutschland GmbH, 2023-10-30T00:00:00) Sain, Rachana; Roy, Ayan; Kumar, Ajay; Anu; Deeksha; Kour, Pawanpreet; Singh, Ravi Pratap; Yadav, Kamlesh
    We synthesized Sm2?xDyxO3 (where X = 0.00, 0.03, 0.06, 0.09, and 0.12) nanoparticles using a co-precipitation method and investigated their structural and optical properties. X-ray diffraction (XRD) results reveal that Dy3+-doping in Sm2O3 nanoparticles leads to the formation of a monoclinic polymorphic phase along with the cubic phase of Sm2O3 and its fraction increases with increasing Dy3+-doping concentration. The substitution of Dy3+ at the Sm3+ site converts the cubic Sm2O3 unit cells into distorted monoclinic Sm2?XDyXO3 unit cells. The average crystallite and nanoparticle sizes decrease with increasing Dy3+-doping concentration. Dy3+-ions act as particle size inhibitors, which is attributed to an increase in the segregation of Dy3+-dopant ions at the surface of the nanoparticles with increasing Dy3+-doping content. The peak appearing at 851�cm?1 in the Fourier transform infrared spectroscopy (FTIR) spectra confirms the formation of Sm2O3. Widening of the band gap (Eg) above the band gap of pure cubic Sm2O3 with Dy3+-doping concentration has been observed for X > 0.06, which is due to the Moss-Burstein and quantum size effects. � 2023, The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.
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    Effects of interfacial interactions on structural, optical, thermal degradation properties and photocatalytic activity of low-density polyethylene/BaTiO3 nanocomposite
    (Elsevier Ltd, 2023-04-10T00:00:00) Roy, Ayan; Panda, Sambit; Gupta, Jaya; Anu; Singh, Ravi Pratap; Deeksha; Kour, Pawanpreet; Sharma, M.P.; Yadav, Kamlesh
    Barium titanate (BaTiO3) filled low density polyethylene (LDPE), (LDPE)100?x/(BaTiO3)x (where x = 0, 2, 4, 6 and 10) nanocomposites are prepared via a solvent-free melt-mixing method. The effects of nano-sized BaTiO3 (nBT) on the structural, optical and thermal degradation properties of LDPE are investigated to address the qualitative interfacial interaction effects due to the spatial distribution of nBT particles in the LDPE matrix. X-ray diffraction (XRD) results confirm the uniform dispersion of nBT nano-fillers in the LDPE polymer matrix. The crystallite size of LDPE increases with increasing the nBT content. Fourier transform infrared spectroscopy (FTIR) results indicate the enhancement in interfacial physical interactions between the polymer and nano-fillers with increasing nano-filler content. The band gap energy of the nanocomposites decreases with increasing nano-filler content, which suggests chemical imperfections close to the interfaces. DSC results depict higher Tm values for the composites which is attributed to the heterogeneous nucleating effects of the nBT particles. Thermo-gravimetric analysis (TGA) results indicate an increase in the decomposition temperature (TD), thermal stability and good dispersibility probability of nBT with increasing nBT. The photocatalytic decomposition of MB is highest (73.52%) for the 10% nBT incorporated LDPE nanocomposite sample. These results correlate with the effect of the interfacial interactions between the nBT fillers and the LDPE polymer matrix. � 2023 Elsevier Ltd
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    Effects of Interfacial Interactions and Nanoparticle Agglomeration on the Structural, Thermal, Optical, and Dielectric Properties of Polyethylene/Cr2O3 and Polyethylene/Cr2O3/CNTs Nanocomposites
    (Springer, 2022-11-22T00:00:00) Gupta, Jaya; Kumar, Ajay; Roy, Ayan; Anu; Deeksha; Kour, Pawanpreet; Singh, Ravi Pratap; Yogesh, Gaurav Kumar; Yadav, Kamlesh
    In this report, we have synthesized the binary and ternary phase nanocomposites [(polyethylene (PE)1?X/(Cr2O3)x) and (PE)1?X/(Cr2O3)X/CNTs (where X = 0,�2%, 4%, 6%, 8%, and 10%)] using the melt mixing method and studied the structural, optical, thermal and dielectric properties with an increase in Cr2O3 nanofiller concentration. Our results show an increase in interfacial interactions between Cr2O3 nanofiller and PE matrix with an increase in nanofiller concentration up to X = 6%. After that, the interactions decreased with a further increase in X because of the increase in the size of the Cr2O3 nanoparticle aggregates. Incorporating 2% carbon nanotubes (CNTs) into (PE)1?X/(Cr2O3)X nanocomposites, further decreases the interactions between the Cr2O3 nanofiller and the PE matrix. � 2022, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
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    Bifunctional electrochemical OER and HER activity of Ta2O5 nanoparticles over Fe2O3 nanoparticles
    (Royal Society of Chemistry, 2023-08-23T00:00:00) Ahmed, Imtiaz; Burman, Vishal; Biswas, Rathindranath; Roy, Ayan; Sharma, Rohit; Haldar, Krishna Kanta
    Hydrogen production via electrocatalytic water splitting offers encouraging innovations for sustainable and clean energy production as an alternative to conventional energy sources. The improvement of extraordinarily dynamic electrocatalysts is of great interest for work on the performance of gas generation, which is firmly blocked due to the sluggish kinetics of the oxygen evolution reaction (OER). The development of highly efficient base metal catalysts for electrochemical hydrogen and oxygen evolution reactions (HER and OER) is a challenging and promising task. In the present work, a particle over particles of Fe2O3 and Ta2O5 was successfully produced by hydrothermal treatment. The prepared composite shows promising catalytic performance when used as an electrochemical catalyst for OER and HER in alkaline and acidic electrolytes with low overpotentials of 231 and 201 mV at 10 mV cm?2, small Tafel slopes of 71 and 135 mV dec?1, respectively, and good stability properties. The calculated electrochemical surface area (ECSA) for composites is five times higher than that of the original oxides. The result of the OER is significantly better than that of commercial IrO2 catalysts and offers a promising direction for the development of water-splitting catalysts. � 2023 The Royal Society of Chemistry.
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    NiS/MoS2 Anchored Multiwall Carbon Nanotube Electrocatalyst for Hydrogen Generation and Energy Storage Applications
    (John Wiley and Sons Inc, 2023-04-05T00:00:00) Ahmed, Imtiaz; Biswas, Rathindranath; Iqbal, Muzahir; Roy, Ayan; Haldar, Krishna Kanta
    Although sulfide-based materials are known to be efficient catalysts for oxygen evolution reactions (OER), hydrogen evolution reactions (HER), and supercapacitor applications, improving the catalytic activity of sulfide materials for both electrochemical water splitting and supercapacitors remains a challenging problem. Here, an easy and one-step integrated methodology is implemented to develop NiS/MoS2 anchored multiwall carbon nanotubes (MWCNT/NiS/MoS2) catalysts that can effectively and robustly catalyze both the HER and OER. The MWCNT/NiS/MoS2 hybrid composite offers the lowest overpotential of 201 mV and 193 mV to achieve a current density of 10 mA/cm2 and ?10 mA/cm2 with a small Tafel slope of 58 mV/dec 41 mV/dec for OER and HER, respectively, in alkaline and acidic conditions. The obtained multi-walled carbon nanotubes anchored with intertwined NiS/MoS2 have a significant number of active sites and defects throughout the structure. The hybrid composite electrode delivered a specific capacitance of >371.45 F/g at 2 A/g in a two-electrode system, along with high energy density of 51.63 Wh/kg (ED) along with the power density (PD) of 953.63 W/kg, and good capacitance retention ?82% after 2000 cycles. Therefore, a tandem electron transfer mechanism between NiS and MoS2 (MoS2?NiS) is believed to have an electrical synergistic effect that promotes both HER and OER activity. This research opens a new path for the construction of multi-component, cheap electrocatalysts that are highly effective for overall water splitting and energy storage applications. � 2023 Wiley-VCH GmbH.