Cobalt oxysulphide/hydroxide nanosheets with dual properties based on electrochromism and a charge storage mechanism.
Ontology highlight
ABSTRACT:
SUBMITTER: Kalasina S
PROVIDER: S-EPMC9051897 | biostudies-literature | 2020 Apr
REPOSITORIES: biostudies-literature
Publications
Cobalt oxysulphide/hydroxide nanosheets with dual properties based on electrochromism and a charge storage mechanism.
Kalasina Saran S Kongsawatvoragul Ketsuda K Phattharasupakun Nutthaphon N Phattharaphuti Phitchayapha P Sawangphruk Montree M
RSC advances 20200407 24
The charge storage mechanism of mixed cobalt oxysulphide/hydroxide materials having electrochromic properties was investigated. The cobalt oxysulphide/hydroxide materials exhibit a dual reversible redox reaction and electrochromic properties in 1 M KOH during charging and discharging. ...[more]
Similar Datasets
Project description:Cobalt hydroxide is a promising electrode material for supercapacitors due to the high capacitance and long cyclability. However, the energy storage/conversion mechanism of cobalt hydroxide is still vague at the atomic level. Here we shed light on how cobalt hydroxide functions as a supercapacitor electrode at operando conditions. We find that the high specific capacitance and long cycling life of cobalt hydroxide involve a complete modification of the electrode morphology, which is usually believed to be unfavourable but in fact has little influence on the performance. The conversion during the charge/discharge process is free of any massive structural evolution, but with some tiny shuffling or adjustments of atom/ion species. The results not only unravel that the potential of supercapacitors could heavily rely on the underlying structural similarities of switching phases but also pave the way for future material design for supercapacitors, batteries and hybrid devices.
| S-EPMC5424148 | biostudies-literature
Project description:High-grade serous ovarian cancer (HGSOC) is one of the major life-threatening cancers in women, with a survival rate of less than 50%. So far, chemotherapy is the main therapeutic tool to cure this lethal disease; however, in many cases, it fails to cure HGSOC even with severe side effects. Self-therapeutic nanomaterials could be an effective alternative to chemotherapy, facilitated by their diverse physicochemical properties and the ability to generate reactive species for killing cancer cells. Herein, inorganic cobalt hydroxide nanosheets (Co(OH)2 NS) were synthesized by a simple solution process at room temperature, and morphological, spectroscopic, and crystallographic analyses revealed the formation of Co(OH)2 NS with good crystallinity and purity. The as-prepared Co(OH)2 NS showed excellent potency, comparable to the FDA-approved cisplatin drug to kill ovarian cancer cells. Flow cytometric analysis (nnexin V) revealed increased cellular apoptosis for Co(OH)2 NS than cobalt acetate (the precursor). Tracking experiments demonstrated that Co(OH)2 NS are internalized through the lysosome pathway, although relocalization in the cytoplasm has been observed. Hence, Co(OH)2 NS could be an effective self-therapeutic drug and open up an area for the optimization of self-therapeutic properties of cobalt nanomaterials for cancer treatment.
| S-EPMC8567285 | biostudies-literature
Project description:We report a one-pot method for the preparation of graphene-cobalt hydroxide nanosheets (Co/G NSs) and their use as an effective elelctrocatalyst for water oxidation. Mechanical exfoliation of graphite via sonication produced graphene sheets, which were stabilized by the surface adsorption of a cationic surfactant (CTAB). In a subsequent step, varying amount of a cobalt complex [sodium hexanitrocobaltate(III)] was added which selectively bound with the positively charged head of surfactant. In the last step, cobalt complex was reduced with sodium borohydride to obtain Co/G NSs catalyst. The catalyst showed lower overpotential (280 mV) as compared to benchmark catalysts and decent stability and turnover frequency (TOF: 0.089 s-1) for oxygen evolution reaction (OER).
| S-EPMC6137037 | biostudies-literature
Project description:Faradaic electrode materials have significantly improved the performance of membrane capacitive deionization, which offers an opportunity to produce freshwater from seawater or brackish water in an energy-efficient way. However, Faradaic materials hold the drawbacks of slow desalination rate due to the intrinsic low ion diffusion kinetics and inferior stability arising from the volume expansion during ion intercalation, impeding the engineering application of capacitive deionization. Herein, a pseudocapacitive material with hollow architecture was prepared via template-etching method, namely, cuboid cobalt hydroxide, with fast desalination rate (3.3 mg (NaCl)·g-1 (h-Co(OH)2)·min-1 at 100 mA·g-1) and outstanding stability (90% capacity retention after 100 cycles). The hollow structure enables swift ion transport inside the material and keeps the electrode intact by alleviating the stress induced from volume expansion during the ion capture process, which is corroborated well by in situ electrochemical dilatometry and finite element simulation. Additionally, benefiting from the elimination of unreacted bulk material and vertical cobalt hydroxide nanosheets on the exterior surface, the synthesized material provides a high desalination capacity (117 ± 6 mg (NaCl)·g-1 (h-Co(OH)2) at 30 mA·g-1). This work provides a new strategy, constructing microscale hollow faradic configuration, to further boost the desalination performance of Faradaic materials.
| S-EPMC8566195 | biostudies-literature
Project description:To make full use of sunlight for water splitting reactions for hydrogen production, a visible-light-driven photocatalyst was developed by modifying TiO2 nanosheets with Co(OH)2. By adding an aqueous Co(NO3)2·6H2O solution to a TiO2 nanosheet suspension, the TiO2 nanosheets aggregated and Co(OH)2 was formed. In the ultraviolet-visible (UV-vis) diffuse reflectance spectrum of the photocatalyst, new absorption bands attributable to Co(OH)2 and the interfacial charge transfer between Co(OH)2 and the TiO2 nanosheets appeared at around 600 and 400 nm, respectively. The photocatalytic activity of Co(OH)2/TiO2 nanosheets was evaluated in terms of the O2 evolution reaction in an aqueous AgNO3 solution, finding that the reaction proceeds under visible light. Furthermore, the investigation of the wavelength dependence of the photocatalytic activity revealed that the photocatalytic reaction on Co(OH)2/TiO2 nanosheets proceeds via Co(OH)2 photocatalysis and interfacial charge transfer between Co(OH)2 and the TiO2 nanosheets under visible light irradiation.
| S-EPMC11780558 | biostudies-literature
Project description:Inspired by the biological metabolic process, some biomolecules with reversible redox functional groups have been used as promising electrode materials for rechargeable batteries, supercapacitors and other charge-storage devices. Although these biomolecule-based electrode materials possess remarkable beneficial properties, their controllable synthesis and morphology-related properties have been rarely studied. Herein, one dimensional nanostructures based on juglone biomolecules have been successfully fabricated by an antisolvent crystallization and self-assembly method. Moreover, the size effect on their electrochemical charge-storage properties has been investigated. It reveals that the diameters of the one dimensional nanostructure determine their electron/ion transport properties, and the juglone nanowires achieve a higher specific capacitance and rate capability. This work will promote the development of environmentally friendly and high-efficiency energy storage electrode materials.
| S-EPMC9077263 | biostudies-literature
Project description:Although cobalt hydroxide (Co(OH)2) has been attracting attention in several applications, its photoelectrochemical property has not yet been fully investigated. In this work, tuning the energy band gap of Co(OH)2 nanosheets with silver atoms and enhancing their electrical conductivity with silver nanoparticles were then focused. A Ag-doped α-Co(OH)2 thin film was successfully synthesized via an electrodeposition method. The optical properties of the as-prepared materials were characterized by UV-vis and fluorescence lifetime spectroscopies and further confirmed by density functional theoretical calculation. It was found that Ag atoms between adjacent layers of Co(OH)2 can reduce its electronic band gap to 2.45 eV (α-Co(OH)2) as compared to 2.85 eV of β-Co(OH)2. In terms of electrochemical properties, silver nanoparticles (AgNPs) can enhance the electrical conductivity of Co(OH)2 nanosheets, leading to faster charge transfer reducing the internal resistance and significantly increasing the overall charge storage performance. Interestingly, under light illumination, Ag-doped α-Co(OH)2 exhibits ca. 0.8 times lower charge storage capacity as compared to that under the dark condition. This is because the photoelectrons can be recombined with the generated holes in the conduction band. The charge storage mechanisms of Ag-doped α-Co(OH)2 operated under dark conditions and light irradiation were further studied and confirmed using in situ electrochemical X-ray absorption spectroscopy (XAS). Overall, the in situ XAS supports the electrochemical result. This finding may pave a way to further develop photoactive advanced functional materials of metal hydroxides and oxides.
| S-EPMC8374905 | biostudies-literature
Project description:Novel carbon-free Mn2O3/MnCr2O4 hybrid nanosheets are synthesized through thermal decomposition of the facilely co-precipitated Mn-Cr binary hydroxide and a carbonate hybrid precursor. As an anode for lithium-ion batteries, the Mn2O3/MnCr2O4 electrode delivers a wonderful electrochemical performance, i.e., an enhanced stability of 913 mA h g-1 at a current density of 1 A g-1 after 300 cycles, and an excellent rate performance. The excellent electrochemical performance of the Mn2O3/MnCr2O4 electrode can be ascribed to the interconnected nanosheets and porous structure, as well as the possible synergistic effects between Mn and Cr mixed oxides.
| S-EPMC9085269 | biostudies-literature
Project description:Decoupling energy supply from fossil fuels through electrification and sustainable energy management requires efficient and environmentally low-impact energy storage technologies. Potential candidates are charge storage electrodes that combine nickel and cobalt hydroxides with reduced graphene oxide (rGO) designed to achieve high-energy, high-power density and long cycling lifetimes. An early eco-efficiency analysis of these electrodes seeks to examine the impacts of materials and processes used in the synthesis, specifically while focusing on the use of rGO. The emerging electrodes synthesized by means of electrodeposition, are further compared with electrodes obtained by an alternative synthesis route involving co-precipitation. Life cycle assessment (LCA) method was applied to compare a baseline nickel-cobalt hydroxide electrode (NCED), the focal electrode integrating rGO (NCED-rGO), and the benchmark co-precipitated electrode (NCCP), for delivering the charge of 1000 mA h. Contribution analysis reveals that the main environmental hotspots in the synthesis of the NCED-rGO are the use of electricity for potentiostat, ethanol for cleaning, and rGO. Results of comparison show significantly better performance of NCED-rGO in comparison to NCED across all impact categories, suggesting that improved functionalities by addition of rGO outweigh added impacts of the use of material itself. NCED-rGO is more impactful than NCCP except for the indicators of cumulative energy demand, climate change, and fossil depletion. To produce a functional equivalent for the three electrodes, total cumulative energy use was estimated to be 78 W h for NCED, 25 W h for NCED-rGO, and 35 W h for NCCP. Sensitivity analysis explores the significance of rGO efficiency uptake on the relative comparison with NCCP, and potential impact of rGO on the category of freshwater ecotoxicity given absence of removal from the process effluent. Scenario analysis further shows relative performance of the electrodes at the range of alternative functional parameters of current density and lifetime. Lastly, the environmental performance of NCED-rGO electrodes is discussed in regard to technology readiness level and opportunities for design improvements.
| S-EPMC9065049 | biostudies-literature
Project description:Optical recording based on voltage-sensitive fluorescent reporters allows for spatial flexibility of measuring from desired cells, but photobleaching and phototoxicity of the fluorescent labels often limit their sensitivity and recording duration. Voltage-dependent optical absorption, rather than fluorescence, of electrochromic materials, would overcome these limitations to achieve long-term optical recording of bioelectrical signals. Electrochromic materials such as PEDOT:PSS possess the property that an applied voltage can either increase or decrease the light absorption depending on the wavelength. In this work, we harness this anticorrelated light absorption at two different wavelengths to significantly improve the signal detection. With dual-color detection, electrical activity from cells produces signals of opposite polarity, while artifacts, mechanical motions, and technical noises are uncorrelated or positively correlated. Using this technique, we are able to optically record cardiac action potentials with a high signal-to-noise ratio, 10 kHz sampling rate, >15 min recording duration, and no time-dependent degradation of the signal. Furthermore, we can reliably perform multiple recording sessions from the same culture for over 25 days.
| S-EPMC9801420 | biostudies-literature