Advances in the Internet of Things (IoT) technology have driven the demand for miniaturized electronic devices, prompting research on small-scale energy-storage systems. Micro-supercapacitors (MSCs) stand out in this regard because of their compact size, high power density, high charge-discharge rate, and extended cycle life. However, their limited energy density impedes commercialization. To resolve this issue, a simple and innovative approach is reported herein for fabricating highly efficient on-chip MSCs integrated with nanoporous metal microwires formed by dielectrophoresis (DEP)-driven gold nanoparticle (AuNP) assembly. Placing a water-based AuNP suspension onto interdigitated electrodes and applying an alternating voltage induces in-plane porous microwire formation in the electrode gap. The DEP-induced AuNP assembly and the gold microwire (AuMW) growth rate can be adjusted by controlling the applied alternating voltage and frequency. The microwire-integrated MSC (AuMW-MSC) electrically outperforms its unmodified counterpart and exhibits a 30% larger electrode area, along with 72% and 78% higher specific and areal capacitances, respectively, than a microwire-free MSC. Additionally, AuMW-MSC achieves maximum energy and power densities of 3.33 µWh cm and 2629 µW cm, respectively, with a gel electrolyte. These findings can help upgrade MSCs to function as potent energy-storage devices for small electronics.
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http://dx.doi.org/10.1002/smll.202311726 | DOI Listing |
J Biomol Struct Dyn
March 2025
Department of Chemistry, Jamia Millia Islamia, New Delhi, India.
1,3,4-Oxadiazole-based heterocyclic analogs (3a-3m) were synthesized cyclization of Schiff bases with substituted aldehydes in the presence of bromine and acetic acid. The structural clarification of synthesized molecules was carried out with various spectroscopic techniques such as FT-IR,H and C-NMR, UV-visible spectroscopy, and mass spectrometry. antifungal activity was performed against , and and analogs 3g, 3i, and 3m showed potent MIC at 200 µg/ml and excellent ZOI measurements of 17-21 nm.
View Article and Find Full Text PDFNanoscale Adv
January 2025
School of Chemical Engineering, Yeungnam University 280 Daehak-Ro Gyeongsan 38541 Republic of Korea
Two-dimensional (2D) hybrid materials, particularly those based on boron nitride (BN) and graphene oxide (GO), have attracted significant attention for energy applications owing to their distinct structural and electronic properties. BN/GO composites uniquely combine the mechanical strength, thermal stability and electrical insulation of BN with the high conductivity and flexibility of GO, creating advanced materials ideal for the fabrication of batteries, supercapacitors and fuel cells. These hybrids offer synergistic effects, enhanced charge transport, increased surface area, and improved chemical stability, making them promising candidates for high-performance energy systems.
View Article and Find Full Text PDFJACS Au
January 2025
Department of Chemistry and Applied Biosciences, ETH Zürich, CH-8093 Zurich, Switzerland.
Hydrogenation of CO to methanol is foreseen as a key step to close the carbon cycle. In this study, we show that introducing Ga into silica-supported nanoparticles based on group 8-9 transition noble metals (M = Ru, Os, Rh, and Ir - Ga@SiO) switches their reactivity from producing mostly methane (sel. > 97%) to producing methanol (>50% CHOH/DME sel.
View Article and Find Full Text PDFJACS Au
January 2025
School of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Mechanochemistry and mechanocatalysis are gaining increasing attention as environmentally friendly chemical processes because of their solvent-free nature and scalability. Significant effort has been devoted for studying continuum-scale phenomena in mechanochemistry, such as temperature and pressure gradients, but the atomic-scale mechanisms remain relatively unexplored. In this work, we focus on the mechanochemical reduction of MoO as a case study.
View Article and Find Full Text PDFJACS Au
January 2025
Department of Chemical and Biomolecular Engineering, University of Houston, Houston, Texas 77204, United States.
The influence of high-intensity electric fields on the stability of polymeric materials is a problem of interest in the design of next-generation energy storage and electronic devices, and for understanding the limits of stability of polymer films exposed to large electric fields generally. Here, we show that the dielectric strength of entangled glassy polymer films increases as an inverse power-law of the film thickness for "ultrathin" films below a micron in thickness. The dielectric strength enhancement in these polymer films becomes as large as ≈2 GV/m in films thinner than 100 nm, but in this thickness regime, the increase of the dielectric strength depends strongly on the polymer mass, sample aging time, and the method of film preparation.
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