Department Of Chemistry

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    Efficient MoS2/V2O5 Electrocatalyst for Enhanced Oxygen and Hydrogen Evolution Reactions
    (Springer, 2023-04-29T00:00:00) Haldar, Krishna Kanta; Ahmed, Imtiaz; Biswas, Rathindranath; Mete, Shouvik; Patil, Ranjit A.; Ma, Yuan-Ron
    Electrochemical (EC) water splitting is a promising approach for the generation of renewable hydrogen (H2) fuels and oxygen (O2) evolution. Composite structured molybdenum disulphide (MoS2)/vanadium pentoxide (V2O5) with low overpotential is a promising electrocatalyst for anodic and cathodic material for an alternative energy source. We fabricated a flower shape MoS2/V2O5 composite via a hydrothermal approach where V2O5grew on the surface of the MoS2 petals. The unique flower-type composite structure alleviates the surface expansion of electrode material. The electrochemical studies show that the composite possesses good stability with low overpotential and smaller Tafel slope compared to its constituents. It has been found that the MoS2/V2O5 composite exhibits a stable rate performance under the current density of 10�mA�cm?2 which indicates that the MoS2/V2O5 composite might be a good candidate for both oxygen and hydrogen evolution reactions.; Graphical Abstract: [Figure not available: see fulltext.] � 2023, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
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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.
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    Tuning the Morphology of Lanthanum Cobaltite Using the Surfactant-Assisted Hydrothermal Approach for Enhancing Oxygen Evolution Catalysis
    (Springer Science and Business Media Deutschland GmbH, 2022-09-01T00:00:00) Deeksha; Kour, Pawanpreet; Ahmed, Imtiaz; Haldar, Krishna Kanta; Yadav, Kamlesh
    The high consumption rate of fossil fuels to meet the global energy demands attracts the progress of innovative energy storage and conversion systems. Among them, water electrolysis shows major concern because of its great potential to produce clean hydrogen energy. The dawdling dynamics of the oxygen evolution reaction (OER) that occurs on the anode results in the low energy efficiency of the process. Perovskite oxide with transition metal on the B site possesses a high intrinsic as well as extrinsic activity toward OER. However, the low specific surface area restricts their catalytic activity. Here, we report on the synthesis of lanthanum cobaltite (LaCoO3) nanoparticles and bundles of nanorods using glycine and PVP surfactants, respectively, via the hydrothermal method. Structural characterizations confirmed the pure phase synthesis of LaCoO3 perovskite nanomaterials and further their electrocatalytic performance is investigated in an alkaline medium (1 M KOH). The results show that randomly oriented bundles of nanorods (average length 515 nm, average diameter 65 nm) exhibit smaller overpotential (? = 420 mV) at j = 10 mA cm?2 and the Tafel slope (99 mV dec?1) compared with nanoparticles (? = 450 mV and Tafel slope ~ 110 mV dec?1). The dramatically improved OER activity and larger electrochemical surface area (ECSA) of nanorods as compared to nanoparticles are because of the interconnected porous architecture of nanorods. Our work not only highlights the surfactant-assisted hydrothermal approach to synthesize the nanorods but also introduces the effect of a change in morphology on electrochemical activity. � 2022, The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd.
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    Dumbbell-Shaped Ternary Transition-Metal (Cu, Ni, Co) Phosphate Bundles: A Promising Catalyst for the Oxygen Evolution Reaction
    (American Chemical Society, 2022-01-27T00:00:00) Singh, Harjinder; Biswas, Rathindranath; Ahmed, Imtiaz; Thakur, Pooja; Kundu, Avinava; Panigrahi, Abhishek Ramachandra; Banerjee, Biplab; Halder, Krishna Kamal; Lahtinen, Jouko; Mondal, Krishnakanta; Haldar, Krishna Kanta
    Development of economical and high-performance electrocatalysts for the oxygen evolution reaction (OER) is of tremendous interest for future applications as sustainable energy materials. Here, a unique member of efficient OER electrocatalysts has been developed based upon structurally versatile dumbbell-shaped ternary transition-metal (Cu, Ni, Co) phosphates with a three-dimensional (3D) (Cu2(OH)(PO4)/Ni3(PO4)2�8H2O/Co3(PO4)2�8H2O) (CNCP) structure. This structure is prepared using a simple aqueous stepwise addition of metal ion source approach. Various structural investigations demonstrate highly crystalline nature of the composite structure. Apart from the unique structural aspect, it is important that the CNCP composite structure has proved to be an excellent electrocatalyst for OER performance in comparison with its binary or constituent phosphate under alkaline and neutral conditions. Notably, the CNCP electrocatalyst displays a much lower overpotential of 224 mV at a current density of 10 mA cm-2 and a lower Tafel slope of 53 mV dec-1 with high stability in alkaline medium. In addition, X-ray photoelectron spectroscopy analysis suggested that the activity and long-term durability for the OER of the ternary 3D metal phosphate are due to the presence of electrochemically dynamic constituents such as Ni and Co and their resulting synergistic effects, which was further supported by theoretical studies. Theoretical calculations also reveal that the incredible OER execution was ascribed to the electron redistribution set off in the presence of Ni and Cu and the most favorable interaction between the *OOH intermediate and the active sites of CNCP. This work may attract the attention of researchers to construct efficient 3D ternary metal phosphate catalysts for various applications in the field of electrochemistry. � 2022 American Chemical Society.
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    Graphitic Carbon Nitride Composites with MoO3-Decorated Co3O4Nanorods as Catalysts for Oxygen and Hydrogen Evolution
    (American Chemical Society, 2021-10-22T00:00:00) Ahmed, Imtiaz; Biswas, Rathindranath; Patil, Ranjit A.; Halder, Krishna Kamal; Singh, Harjinder; Banerjee, Biplab; Kumar, Bhupender; Ma, Yuan-Ron; Haldar, Krishna Kanta
    We have prepared a graphitic carbon nitride (g-C3N4) composite with MoO3-decorated Co3O4 nanorods (Co3O4/MoO3/g-C3N4) via the hydrothermal approach, and this hybrid material acts as a highly active and durable electrocatalyst for water splitting reactions. This material could fundamentally influence the catalytic processes and performance of oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). The OER and HER activities of Co3O4-/MoO3-based nanorods are enhanced by blending with conducting support, for example, graphitic carbon nitrides (g-C3N4). The X-ray diffraction pattern and the attenuated total reflectance-Fourier transform infrared data revealed that the as-synthesized nanorods are highly crystalline in nature and are attached to the g-C3N4 support. Transmission electron microscopy, X-ray photoelectron spectroscopy, and Raman spectroscopy studies also affirm the successful heterointerface formation between Co3O4/MoO3 nanorods and g-C3N4. This Co3O4/MoO3/g-C3N4 rod-shaped catalyst is highly stable in comparison to its individual constituent and generates a current density of 10 mA cm-2 at a low overpotential of 206 mV for OER and 125 mV for HER in alkaline and acidic media, respectively. This work could pave the way for developing Co3O4/MoO3/g-C3N4 composite materials as electrocatalysts for overall water splitting reactions. � 2021 American Chemical Society. All rights reserved.