6 research outputs found

    Recent advances in carbon-based materials for high-performance perovskite solar cells: gaps, challenges and fulfillment

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    Presently, carbon-based nanomaterials have shown tremendous potential for energy conversion applications. Especially, carbon-based materials have emerged as excellent candidates for the fabrication of halide perovskite-based solar cells, which may lead to their commercialization. In the last decade, PSCs have rapidly developed, and these hybrid devices demonstrate a comparable performance to silicon-based solar cells in terms of power conversion efficiency (PCE). However, PSCs lag behind silicon-based solar cells due to their poor stability and durability. Generally, noble metals such gold and silver are employed as back electrode materials during the fabrication of PSCs. However, the use of these expensive rare metals is associated with some issues, urgently necessitating the search for cost-effective materials, which can realize the commercial applications of PSCs due to their interesting properties. Thus, the present review shows how carbon-based materials can become the main candidates for the development of highly efficient and stable PSCs. Carbon-based materials such as carbon black, graphite, graphene nanosheets (2D/3D), carbon nanotubes (CNTs), carbon dots, graphene quantum dots (GQDs) and carbon nanosheets show potential for the laboratory and large-scale fabrication of solar cells and modules. Carbon-based PSCs can achieve efficient and long-term stability for both rigid and flexible substrates because of their high conductivity and excellent hydrophobicity, thus showing good results in comparison to metal electrode-based PSCs. Thus, the present review also demonstrates and discusses the latest state-of-the-art and recent advances for carbon-based PSCs. Furthermore, we present perspectives on the cost-effective synthesis of carbon-based materials for the broader view of the future sustainability of carbon-based PSCs.Validerad;2023;Nivå 2;2023-03-22 (hanlid);Funder: NMHS; GBPHIED (GBPNI/NMHS-2019-20/MG) Kosi-Katarmal, Almora, India; National Research Foundation of Korea (NRF) - Ministry of Education (2022R1F1A1073950)</p

    Synthesis of porous carbon from a PVC polymer and its application in supercapacitors

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    In this study, the laboratory scale production of activated carbon synthesized from PVC with CoCl2 and H3PO4, which is cheaper and has a good yield source material, is reported. A prototype supercapacitor was successfully developed using activated carbon as an electrode material derived from the PVC polymer and IL (1-ethyl-3-methylimidazolium thiocyanate) as the electrolyte. The performance of the supercapacitor was estimated via electrochemical impedance spectroscopy, cyclic voltammetry, and the charge–discharge technique. The supercapacitor offered a high specific capacitance of ∼120 F g−1 at 5 m V s−1. The performances of the supercapacitor were also estimated up to 15 days and up to 9000 cycles via cyclic voltammetry

    Binder-Free Supercapacitors Based on Thin Films of MWCNT/GO Nanohybrids: Computational and Experimental Analysis

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    This work reports an innovative approach to the fabrication of free-standing thin films of multiwalled carbon nanotubes (MWCNTs)/graphene oxide (GO) nanohybrids by using dimethyl formamide (DMF) and n-hexane as a solvent–antisolvent system for the growth of thin films of MWCNTs/GO nanohybrids. The synthesis of the GO was carried out by using the modified Hummers method, while the synthesis of MWCNTs/GO nanohybrids was done by the intermixing of the carboxylic acid functionalized MWCNT and GO using the solution-mixing method. The growth of the thin film of MWCNTs/GO nanohybrids was done by obeying the surface-tension-driven phenomena which occur mainly due to the coalescence of bubbles due to the solvent–antisolvent interfacial tension. Furthermore, density functional theory (DFT)-based first-principles simulations were performed to understand the structural, electronic, and capacitive aspects of MWCNT/GO nanohybrids. The computational results demonstrated excellent quantum capacitance in the MWCNT/GO nanohybrid electrodes. Inspired by the computational results, the same process elaborated above has also been employed to develop binder-free supercapacitor devices utilizing the MWCNT/GO nanohybrid as an electrode material. The electrochemical performance of this electrode in 1 M aqueous H2SO4 demonstrates a good energy density of 21.63 WhKg−1 at a current density of 0.5 Ag−1, with a high specific capacitance of 369.01 F/g at the scan rate of 2 mVs−1 and excellent cyclic stability of 97% for 5000 charge–discharge cycles

    Binder-Free Supercapacitors Based on Thin Films of MWCNT/GO Nanohybrids: Computational and Experimental Analysis

    No full text
    This work reports an innovative approach to the fabrication of free-standing thin films of multiwalled carbon nanotubes (MWCNTs)/graphene oxide (GO) nanohybrids by using dimethyl formamide (DMF) and n-hexane as a solvent&ndash;antisolvent system for the growth of thin films of MWCNTs/GO nanohybrids. The synthesis of the GO was carried out by using the modified Hummers method, while the synthesis of MWCNTs/GO nanohybrids was done by the intermixing of the carboxylic acid functionalized MWCNT and GO using the solution-mixing method. The growth of the thin film of MWCNTs/GO nanohybrids was done by obeying the surface-tension-driven phenomena which occur mainly due to the coalescence of bubbles due to the solvent&ndash;antisolvent interfacial tension. Furthermore, density functional theory (DFT)-based first-principles simulations were performed to understand the structural, electronic, and capacitive aspects of MWCNT/GO nanohybrids. The computational results demonstrated excellent quantum capacitance in the MWCNT/GO nanohybrid electrodes. Inspired by the computational results, the same process elaborated above has also been employed to develop binder-free supercapacitor devices utilizing the MWCNT/GO nanohybrid as an electrode material. The electrochemical performance of this electrode in 1 M aqueous H2SO4 demonstrates a good energy density of 21.63 WhKg&minus;1 at a current density of 0.5 Ag&minus;1, with a high specific capacitance of 369.01 F/g at the scan rate of 2 mVs&minus;1 and excellent cyclic stability of 97% for 5000 charge&ndash;discharge cycles
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