Browse
Submit Data
Databases
API
Help

Dataset Information

31 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Dendritic Nanostructured Waste Copper Wires for High-Energy Alkaline Battery.

ABSTRACT: Rechargeable alkaline batteries (RABs) have received remarkable attention in the past decade for their high energy, low cost, safe operation, facile manufacture, and eco-friendly nature. To date, expensive electrode materials and current collectors were predominantly applied for RABs, which have limited their real-world efficacy. In the present work, we propose a scalable process to utilize electronic waste (e-waste) Cu wires as a cost-effective current collector for high-energy wire-type RABs. Initially, the vertically aligned CuO nanowires were prepared over the waste Cu wires via in situ alkaline corrosion. Then, both atomic-layer-deposited NiO and NiCo-hydroxide were applied to the CuO nanowires to form a uniform dendritic-structured NiCo-hydroxide/NiO/CuO/Cu electrode. When the prepared dendritic-structured electrode was applied to the RAB, it showed excellent electrochemical features, namely high-energy-density (82.42 Wh kg^-1), excellent specific capacity (219 mAh g^-1), and long-term cycling stability (94% capacity retention over 5000 cycles). The presented approach and material meet the requirements of a cost-effective, abundant, and highly efficient electrode for advanced eco-friendly RABs. More importantly, the present method provides an efficient path to recycle e-waste for value-added energy storage applications.

SUBMITTER: Chodankar NR

PROVIDER: S-EPMC7770717 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Defect-Engineered Nanostructured Ni/MOF-Derived Carbons for an Efficient Aqueous Battery-Type Energy Storage Device.

Project description:A Ni-based metal-organic framework (Ni-MOF) has been synthesized using a microwave-assisted strategy and converted to nanostructured Ni/MOF-derived mesoporous carbon (Ni/MOFDC) by carbonization and acid treatment (AT-Ni/MOFDC). The materials are well characterized with Raman, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), and Brunauer-Emmett-Teller (BET), revealing that chemical etching confers on the AT-Ni/MOFDC-reduced average nanoparticle size (high surface area) and structural defects including oxygen vacancies. AT-Ni/MOFDC displays low series resistances and a higher specific capacity (C s) of 199 mAh g-1 compared to Ni/MOFDC (92 mAh g-1). This study shows that the storage mechanism of the Ni-based electrode as a battery-type energy storage (BTES) system can be controlled by both non-faradic and faradic processes and dependent on the sweep rate or current density. AT-Ni/MOFDC reveals mixed contributions at different rates: 75.2% faradic and 24.8% non-faradic contributions at 5 mV s-1, and 34.1% faradic and 65.9% non-faradic at 50 mV s-1. The full BTES device was assembled with AT-Ni/MOFDC as the cathode and acetylene black (AB) as the anode. Compared to recent literature, the AT-Ni/MOFDC//AB BTES device exhibits high energy (33 Wh kg-1) and high power (983 W kg-1) with excellent cycling performance (about 88% capacity retention over 2000 cycles). This new finding opens a window of opportunity for the rational designing of next-generation energy storage devices, supercapatteries, that combine the characteristics of batteries (high energy) and supercapacitors (high power).

| S-EPMC7439376 | biostudies-literature

Waste Windshield-Derived Silicon/Carbon Nanocomposites as High-Performance Lithium-Ion Battery Anodes.

Project description:Silicon has emerged as the most promising high-capacity material for lithium-ion batteries. Waste glass can be a potential low cost and environmentally benign silica resource enabling production of nanosized silicon at the industry level. Windshields are generally made of laminated glass comprising two separate glass bonded together with a layer of polyvinyl butyral sandwiched between them. Herein, silicon/carbon nanocomposites are fabricated from windshields for the first time via magnesiothermic reduction and facile carbonization process using both waste glass and polyvinyl butyral as silica and carbon sources, respectively. High purity reduced silicon has unique 3-dimensional nanostructure with large surface area. Furthermore, the incorporation of carbon in silicon enable to retain the composite anodes highly conductive and mechanically robust, thus providing enhanced cycle stability.

| S-EPMC5772056 | biostudies-literature

Hybrid system for rechargeable magnesium battery with high energy density.

Project description:One of the main challenges of electrical energy storage (EES) is the development of environmentally friendly battery systems with high safety and high energy density. Rechargeable Mg batteries have been long considered as one highly promising system due to the use of low cost and dendrite-free magnesium metal. The bottleneck for traditional Mg batteries is to achieve high energy density since their output voltage is below 2.0 V. Here, we report a magnesium battery using Mg in Grignard reagent-based electrolyte as the negative electrode, a lithium intercalation compound in aqueous solution as the positive electrode, and a solid electrolyte as a separator. Its average discharge voltage is 2.1 V with stable discharge platform and good cycling life. The calculated energy density based on the two electrodes is high. These findings open another door to rechargeable magnesium batteries.

| S-EPMC4502397 | biostudies-literature

Rice husks as a sustainable source of nanostructured silicon for high performance Li-ion battery anodes.

Project description:The recovery of useful materials from earth-abundant substances is of strategic importance for industrial processes. Despite the fact that Si is the second most abundant element in the Earth's crust, processes to form Si nanomaterials is usually complex, costly and energy-intensive. Here we show that pure Si nanoparticles (SiNPs) can be derived directly from rice husks (RHs), an abundant agricultural byproduct produced at a rate of 1.2 × 10(8) tons/year, with a conversion yield as high as 5% by mass. And owing to their small size (10-40 nm) and porous nature, these recovered SiNPs exhibits high performance as Li-ion battery anodes, with high reversible capacity (2,790 mA h g(-1), seven times greater than graphite anodes) and long cycle life (86% capacity retention over 300 cycles). Using RHs as the raw material source, overall energy-efficient, green, and large scale synthesis of low-cost and functional Si nanomaterials is possible.

| S-EPMC3665957 | biostudies-literature

Highly Efficient Nanocarbon Coating Layer on the Nanostructured Copper Sulfide-Metal Organic Framework Derived Carbon for Advanced Sodium-Ion Battery Anode.

Project description:High theoretical capacity and low-cost copper sulfide (CuxS)-based anodes have gained great attention for advanced sodium-ion batteries (SIBs). However, their practical application may be hindered due to their unstable cycling performance and problems with the dissolution of sodium sulfides (NaxS) into electrolyte. Here, we employed metal organic framework (MOF-199) as a sacrificial template to fabricate nanoporous CuxS with a large surface area embedded in the MOF-derived carbon network (CuxS-C) through a two-step process of sulfurization and carbonization via H2S gas-assisted plasma-enhanced chemical vapor deposition (PECVD) processing. Subsequently, we uniformly coated a nanocarbon layer on the Cu1.8S-C through hydrothermal and subsequent annealing processes. The physico-chemical properties of the nanocarbon layer were revealed by the analytical techniques of high-resolution transmission electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (EDS), and scanning electron microscopy (SEM). We acquired a higher SIB performance (capacity retention (~93%) with a specific capacity of 372 mAh/g over 110 cycles) of the nanoporous Cu1.8S-C/C core/shell anode materials than that of pure Cu1.8S-C. This encouraging SIB performance is attributed to the key roles of a nanocarbon layer coated on the Cu1.8S-C to accommodate the volume variation of the Cu1.8S-C anode structure during cycling, enhance electrical conductivity and prevent the dissolution of NaxS into the electrolyte. With these physico-chemical and electrochemical properties, we ensure that the Cu1.8S-C/C structure will be a promising anode material for large-scale and advanced SIBs.

| S-EPMC6515688 | biostudies-literature

A Carbon- and Binder-Free Nanostructured Cathode for High-Performance Nonaqueous Li-O<sub>2</sub> Battery.

Project description:Operation of the nonaqueous Li-O2 battery critically relies on the reversible oxygen reduction/evolution reactions in the porous cathode. Carbon and polymeric binder, widely used for the construction of Li-O2 cathode, have recently been shown to decompose in the O2 environment and thus cannot sustain the desired battery reactions. Identifying stable cathode materials is thus a major current challenge that has motivated extensive search for noncarbonaceous alternatives. Here, RuO x /titanium nitride nanotube arrays (RuO x /TiN NTA) containing neither carbon nor binder are used as the cathode for nonaqueous Li-O2 batteries. The free standing TiN NTA electrode is more stable than carbon electrode, and possesses enhanced electronic conductivity compared to TiN nanoparticle bound with polytetrafluoroethylene due to a direct contact between TiN and Ti mesh substrate. RuO x is electrodeposited into TiN NTA to form a coaxial nanostructure, which can further promote the oxygen evolution reaction. This optimized monolithic electrode can avoid the side reaction arising from carbon material, which exhibits low overpotential and excellent cycle stability over 300 cycles. These results presented here demonstrate a highly effective carbon-free cathode and further imply that the structure designing of cathode plays a critical role for improving the electrochemical performance of nonaqueous Li-O2 batteries.

| S-EPMC5115428 | biostudies-literature

High-performance hollow sulfur nanostructured battery cathode through a scalable, room temperature, one-step, bottom-up approach.

Project description:Sulfur is an exciting cathode material with high specific capacity of 1,673 mAh/g, more than five times the theoretical limits of its transition metal oxides counterpart. However, successful applications of sulfur cathode have been impeded by rapid capacity fading caused by multiple mechanisms, including large volume expansion during lithiation, dissolution of intermediate polysulfides, and low ionic/electronic conductivity. Tackling the sulfur cathode problems requires a multifaceted approach, which can simultaneously address the challenges mentioned above. Herein, we present a scalable, room temperature, one-step, bottom-up approach to fabricate monodisperse polymer (polyvinylpyrrolidone)-encapsulated hollow sulfur nanospheres for sulfur cathode, allowing unprecedented control over electrode design from nanoscale to macroscale. We demonstrate high specific discharge capacities at different current rates (1,179, 1,018, and 990 mAh/g at C/10, C/5, and C/2, respectively) and excellent capacity retention of 77.6% (at C/5) and 73.4% (at C/2) after 300 and 500 cycles, respectively. Over a long-term cycling of 1,000 cycles at C/2, a capacity decay as low as 0.046% per cycle and an average coulombic efficiency of 98.5% was achieved. In addition, a simple modification on the sulfur nanosphere surface with a layer of conducting polymer, poly(3,4-ethylenedioxythiophene), allows the sulfur cathode to achieve excellent high-rate capability, showing a high reversible capacity of 849 and 610 mAh/g at 2C and 4C, respectively.

| S-EPMC3645569 | biostudies-literature

Dendritic nanostructured FeS<sub>2</sub>-based high stability and capacity Li-ion cathodes.

Project description:Here we show that dendritic architectures are attractive as the basis of hierarchically structured battery electrodes. Dendritically structured FeS2, synthesized via simple thermal sulfidation of electrodeposited dendritic α-Fe, was formed into an electrode and cycled vs. lithium. The reversible capacities of the dendritic FeS2 cathode were 560 mA h g-1 at 0.5C and 533 mA h g-1 at 1.0C after 50 cycles over 0.7-3.0 V. Over 0.7-2.4 V, where the electrode is more stable, the reversible capacities are 348 mA h g-1 at 0.2C and 179 mA h g-1 at 1.0C after 150 cycles. The good cycling performance and high specific capacities of the dendritic FeS2 cathodes are attributed to the ability of a dendritic structure to provide good ion and electron conducting pathways, and a large surface area. Importantly, the dendritic structure appears capable of accommodating volume changes imposed by the lithiation and delithiation process. The presence of a Li2-x FeS2 phase is indicated for the first time by high-resolution transmission electron microscopy (HRTEM) and scanning transmission electron microscopy (STEM) electron energy loss spectroscopy (EELS). We suspect this phase is what enables electrochemical cycling to possess high reversibility over 0.7-2.4 V.

| S-EPMC9090669 | biostudies-literature

Thermal-healing of lattice defects for high-energy single-crystalline battery cathodes.

Project description:Single-crystalline nickel-rich cathodes are a rising candidate with great potential for high-energy lithium-ion batteries due to their superior structural and chemical robustness in comparison with polycrystalline counterparts. Within the single-crystalline cathode materials, the lattice strain and defects have significant impacts on the intercalation chemistry and, therefore, play a key role in determining the macroscopic electrochemical performance. Guided by our predictive theoretical model, we have systematically evaluated the effectiveness of regaining lost capacity by modulating the lattice deformation via an energy-efficient thermal treatment at different chemical states. We demonstrate that the lattice structure recoverability is highly dependent on both the cathode composition and the state of charge, providing clues to relieving the fatigued cathode crystal for sustainable lithium-ion batteries.

| S-EPMC8817033 | biostudies-literature

Nanostructured fuzz growth on tungsten under low-energy and high-flux He irradiation.

Project description:We report the formation of wave-like structures and nanostructured fuzzes in the polycrystalline tungsten (W) irradiated with high-flux and low-energy helium (He) ions. From conductive atomic force microscope measurements, we have simultaneously obtained the surface topography and current emission images of the irradiated W materials. Our measurements show that He-enriched and nanostructured strips are formed in W crystal grains when they are exposed to low-energy and high-flux He ions at a temperature of 1400 K. The experimental measurements are confirmed by theoretical calculations, where He atoms in W crystal grains are found to cluster in a close-packed arrangement between {101} planes and form He-enriched strips. The formations of wave-like structures and nanostructured fuzzes on the W surface can be attributed to the surface sputtering and swelling of He-enriched strips, respectively.

| S-EPMC4468520 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data