ZnS nanoparticles wrapped in N-doped mesoporous carbon nanosheets are prepared from metal-organic frameworks through a simple co-pyrolysis process. In the composite interface, ZnS nanoparticles are directly loaded on the carbon and form a mesoporous structure, thus providing fast electron and ion dual transfer routes, and efficient electrode reaction kinetics. In addition, the heteroatom N-doping and the small-sized ZnS with embedded carbon can provide more active sites and stable electrode kinetics for electrochemical reactions. As a consequence, this material shows a capacity of 160 mA h g-1 at 1 A g-1, and retains 92.9% of its initial capacity after cycling for 1000 times at 5 A g-1. In the assembled asymmetric device, an energy density of 45.5 W h kg-1 is obtained. Such superior properties and facile production process of the metal-organic framework-derived composite show great potential in energy storage.
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http://dx.doi.org/10.1039/c9dt00195f | DOI Listing |
Int J Biol Macromol
January 2025
School of Materials Science and Engineering, School of Chemistry and Chemical Engineering, MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, Harbin Institute of Technology, Harbin 150001, PR China. Electronic address:
Wound bacterial infections not only impede the healing process but can also give rise to a range of serious complications, thereby posing a substantial risk to human health. Developing effective wound dressings incorporating phototherapy functionalities, specifically photothermal therapy (PTT) and photodynamic therapy (PDT), remains a critical area of research in modern wound care. Existing PTT-PDT systems often suffer from challenges such as nanoparticle aggregation and inefficient reactive oxygen species (ROS) generation, which are essential for therapeutic efficacy.
View Article and Find Full Text PDFSci Total Environ
January 2025
School of the Environment, University of Queensland, QLD, Australia.
The transition to net zero emissions requires the capture of carbon dioxide from industrial point sources, and direct air capture (DAC) from the atmosphere for geological storage. Dissolved CO has reactivity to rock core, and while the majority of previous studies have concentrated on reservoir rock or cap-rock reactivity, the underlying seal formation may also react with CO. Drill core from the underlying seal of a target CO storage site was reacted at in situ conditions with pure CO, and compared with an impure CO stream with SO, NO and O that could be expected from hard to abate industries.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
School of Chemistry and Chemical Engineering, Zhejiang Sci-Tech University, 928 Second Street, Hangzhou 310018 China; Zhejiang Sci-Tech University Shengzhou Innovation Research Institute, Shengzhou 312400, China. Electronic address:
To boost supercapacitor (SC) energy density, we introduced redox-active molecules into an aqueous HSO electrolyte. Using retrosynthetic analysis, we identified aminoquinones, specifically triaminochlorobenzoquinone (TACBQ), as promising candidates. Characterization via elemental analysis, Fourier Transform Infrared Spectrometer (FT-IR), nuclear magnetic resonance (NMR), and X-ray photoelectron spectroscopy (XPS) confirmed structure of TACBQ.
View Article and Find Full Text PDFSmall
January 2025
SUNAG Laboratory, Institute of Physics, Sachivalaya Marg, Bhubaneswar, 751 005, India.
Understanding the resistive switching (RS) behavior of oxide-based memory devices at nanoscale is crucial for advancement of high-integration density in-memory computing platforms. This study explores a comprehensive growth parameter space to address the RS behavior of pulsed-laser-deposited substoichiometric TiO (TiO) thin films in search of tailored nanoscale memristors with low-power consumption and high stability. Conductive-atomic-force-microscopy-based measurements facilitate deciphering the switching behavior at nanoscale, providing a direct avenue to understand the microstructure-property relationships.
View Article and Find Full Text PDFSmall
January 2025
State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin, 130022, China.
The scarcity of cost-effective and durable iridium-free anode electrocatalysts for the oxygen evolution reaction (OER) poses a significant challenge to the widespread application of the proton exchange membrane water electrolyzer (PEMWE). To address the electrochemical oxidation and dissolution issues of Ru-based electrocatalysts, an electron-donating modification strategy is developed to stabilize WRuO under harsh oxidative conditions. The optimized catalyst with a low Zirconium doping (Zr, 1 wt.
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