Herein, we report an effective approach to electricity storage in biofuels by selective electrocatalytic reduction of levulinic acid (LA) to high-energy-density valeric acid (VA) or γ-valerolactone (gVL) on a non-precious Pb electrode in a single-polymer electrolyte membrane electrocatalytic (flow) cell reactor with a very high yield of VA (>90 %), a high Faradaic efficiency (>86 %), promising electricity storage efficiency (70.8 %), and a low electricity consumption (1.5 kWhL(VA)(-1) ). The applied potential and electrolyte pH can be used to accurately control the reduction products: lower overpotentials favor the production of gVL, whereas higher overpotentials facilitate the formation of VA. A selectivity of 95 % to VA in acidic electrolyte (pH 0) and 100 % selectivity to gVL in neutral electrolyte (pH 7.5) are obtained. The effect of the molecular structure on the electrocatalytic reduction of ketone and aldehyde groups of biomass compounds was investigated. Whereas LA can be fully electroreduced to VA though a four-electron transfer, the C-O groups are only electroreduced to -OH by a two-electron-transfer process when glyoxylic acid and pyruvic acid serve as feedstocks.
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http://dx.doi.org/10.1002/cssc.201200765 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Department of Physics, School of Electrical and Electronics Engineering, SASTRA Deemed to be University, Thanjavur 613 401, Tamil Nadu, India.
This study presents the fabrication of highly conducting Au fabric electrodes using a layer-by-layer (LBL) approach and its application toward energy storage. Through the ligand-exchange mechanism, the alternating layers of tris(2-aminoethyl)amine (TREN) and gold nanoparticles (Au NPs) encapsulated with tetraoctylammonium bromide (TOABr) ligands (Au-TOABr) were deposited onto the fabric to achieve a highly conducting Au fabric (0.12 Ω/□) at room temperature in just two LBL cycles.
View Article and Find Full Text PDFNano Lett
January 2025
Shanghai, China State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China.
Metal sulfide electrodes for sodium-ion batteries face trade-offs among high capacity, fast kinetics, and stability. The challenge lies in breaking and restoring metal-sulfur bonds and allowing rapid ionic transport. Here we explore the boundary of conversion- and intercalation-type metal sulfides to develop ideal sodium-ion storage materials.
View Article and Find Full Text PDFNanoscale
January 2025
Department of Electrical and Computer Engineering, National University of Singapore, 4 Engineering Drive 3, Singapore 117583.
The widespread proliferation and increasing use of portable electronic devices and wearables, and the recent developments in artificial intelligence and internet-of-things, have fuelled the need for high-density and low-voltage non-volatile memory devices. Nanocrystal memory, an emergent non-volatile memory (NVM) device that makes use of the Coulomb blockade effect, can potentially result in the scaling of the tunnel dielectric layer to a very small thickness. Since the nanocrystals are electrically isolated, potential charge leakage paths localized defects in the thin tunnel dielectric can be substantially reduced, unlike that in a continuous polysilicon floating gate structure.
View Article and Find Full Text PDFDalton Trans
January 2025
Key Laboratory for Photonic and Electronic Bandgap Materials, Ministry of Education, School of Physics and Electronic Engineering, Harbin Normal University, Harbin 150025, People's Republic of China.
A binder-free and freestanding electrode was designed by uniformly immobilizing carbon quantum dot (CQD)-anchored polyaniline (PANI) heterostructures onto electrospun carbon nanofibers (CNFs) a facile hierarchical assembly process. The fabricated freestanding CNF/PANI/CQD electrode exhibits a unique three-dimensional (3D) network nanostructure, which accelerates ion migration between the interior and surface of the electrode, thereby enhancing its charging and discharging performance. Moreover, the functional groups on the surface of CQDs could anchor PANI through possible chemical bonding, which not only improves the stability of the PANI/CQD heterojunction but also creates an additional conductive channel for the PANI polymer.
View Article and Find Full Text PDFMolecular junctions (MJs) are celebrated nanoelectronic devices for mimicking conventional electronic functions, including rectifiers, sensors, wires, switches, transistors, negative differential resistance, and memory, following an understanding of charge transport mechanisms. However, capacitive nanoscale molecular junctions are rarely seen. The present work describes electrochemically (E-Chem) grown covalently attached molecular thin films of 10, 14.
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