Publications by authors named "Muhammad Hilmy Alfaruqi"

Lithium-sulfur (Li-S) batteries using LiS and Li-free anodes have emerged as a potential high-energy and safe battery technology. Although the operation of Li-S full batteries based on LiS has been demonstrated at room temperature, their effective use at a subzero temperature has not been realized due to the low electrochemical utilization of LiS. Here, ammonium nitrate (NHNO) is introduced as a functional additive that allows Li-S full batteries to operate at -10 °C.

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Batteries using potassium metal (K-metal) anode are considered a new type of low-cost and high-energy storage device. However, the thermodynamic instability of the K-metal anode in organic electrolyte solutions causes uncontrolled dendritic growth and parasitic reactions, leading to rapid capacity loss and low Coulombic efficiency of K-metal batteries. Herein, an advanced electrolyte comprising 1 M potassium bis(fluorosulfonyl)imide (KFSI) + 0.

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Manganese (Mn)-based cathode materials have garnered huge research interest for rechargeable aqueous zinc-ion batteries (AZIBs) due to the abundance and low cost of manganese and the plentiful advantages of manganese oxides including their different structures, wide range of phases, and various stoichiometries. A novel in situ generated Mn-deficient ZnMnO@C (Mn-d-ZMO@C) nanoarchitecture cathode material from self-assembly of ZnO-MnO@C for rechargeable AZIBs is reported. Analytical techniques confirm the porous and crystalline structure of ZnO-MnO@C and the in situ growth of Mn deficient ZnMnO@C.

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Lithium-ion batteries (LIBs) are widely used in various electronic devices and have garnered a huge amount of attention. In addition, evaluation of the intrinsic properties of LIB cathode materials is of considerable interest for practical applications. Therefore, through first-principles calculations based on the density functional theory, we investigated the structural, electronic, electrochemical, and kinetic properties of mixed transition metals, that is, Ni-substituted LiMnPO (LMP) and LiMnPOF (LMPF) cathode materials, that is, LiMnNiPO (LMNP) and LiMnNiPOF (LMNPF), respectively, which have not been extensively studied.

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Herein, we synthesize a nanostructured bismuth sulfide/carbon nanotube composite and demonstrate its potential use as a high-capacity anode for K-ion batteries, for the first time. The composite anode shows reversible K-ion storage capabilities that are supported by density functional theory calculations.

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A simple one-pot polyol-assisted pyro-technique has been adopted to synthesize highly crystalline, carbon-coated LiMnO (LMO/C) nanoparticles for use as a cathode material in rechargeable Li-ion battery (LIB) applications. The phase purity, structure and stoichiometry of the prepared cathode was confirmed using X-ray techniques that included high-resolution powder X-ray diffraction and X-ray absorption fine structure spectroscopy. Electron microscopy studies established that the synthetic technique facilitated the production of nano-sized LMO particles with uniform carbon coating.

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Reduced graphene oxide (rGO) sheets were synthesized by a modified Hummer's method without additional reducing procedures, such as chemical and thermal treatment, by appropriate drying of graphite oxide under ambient atmosphere. The use of a moderate drying temperature (250°C) led to mesoporous characteristics with enhanced electrochemical activity, as confirmed by electron microscopy and N adsorption studies. The dimensions of the sheets ranged from nanometres to micrometres and these sheets were entangled with each other.

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We explore NaV6O15 (NVO) nanorod cathodes prepared by a sol-gel method for aqueous rechargeable zinc-ion battery applications for the first time. The NVO cathode delivers a high capacity of 427 mA h g-1 at 50 mA g-1 current density. Furthermore, based on the mass of the active materials, it exhibits a high energy density of 337 W h kg-1.

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Rechargeable hybrid aqueous batteries (ReHABs) have emerged as promising sustainable energy-storage devices because all components are environmentally benign and abundant. In this study, a carbon-wrapped sponge-like Na V (PO ) nanoparticle (NVP@C) cathode is prepared by a simple pyrosynthesis for use in the ReHAB system with impressive rate capability and high cyclability. A high-resolution X-ray diffraction study confirmed the formation of pure Na ion superionic conductor (NASICON) NVP with rhombohedral structure.

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Pyrite (FeS2) is a promising electrode material for lithium ion batteries (LIBs) because of its high natural availability, low toxicity, cost-effectiveness, high theoretical capacity (894 mA h g-1) and high theoretical specific energy density (1270 W h kg-1, 4e-/FeS2). Nevertheless, the use of FeS2 in electrochemical capacitors was restricted due to fast capacity fading as a result of polysulfide (S/Sn2-) formation during the initial electrochemical cycling. In order to avoid the formation of polysulfides, we employed the strategy of utilizing an ether based electrolyte (1.

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Herein, we report on a high-discharge-rate NaV(PO)-NiP/C (NVP-NP/C) composite cathode prepared using a polyol-based pyro synthesis for Na-ion battery applications. X-ray diffraction and electron microscopy studies established the presence of NaV(PO) and NiP, respectively, in the NVP-NP/C composite. As a cathode material, the obtained NVP-NP/C composite electrode exhibits higher discharge capacities (100.

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A nanostructured Mn O /C electrode was prepared by a one-step polyol-assisted pyro-synthesis without any post-heat treatments. The as-prepared Mn O /C revealed nanostructured morphology comprised of secondary aggregates formed from carbon-coated primary particles of average diameters ranging between 20 and 40 nm, as evidenced from the electron microscopy studies. The N adsorption studies reveal a hierarchical porous feature in the nanostructured electrode.

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Hierarchical meso-/macroporous anatase TiO2 was synthesized by the hydrolysis of a titanium metal-organic framework precursor followed by calcination in air. This unique porous feature enables the superior rate capability and excellent cycling stability of anatase TiO2 as an anode for rechargeable lithium-ion batteries.

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