Nano-Germanium/polypyrrole composite has been synthesized by chemical reduction method in aqueous solution. The Ge nanoparticles were directly coated on the surface of the polypyrrole. The morphology and structural properties of samples were determined by X-ray diffraction, scanning electron microscopy and transmission electron microscopy. Thermogravimetric analysis was carried out to determine the polypyrrole content. The electrochemical properties of the samples have been investigated and their suitability as anode materials for the lithium-ion battery was examined. The discharge capacity of the Ge nanoparticles calculated in the Ge-polypyrrole composite is 1014 mAh g(-1) after 50 cycles at 0.2 C rate, which is much higher than that of pristine germanium (439 mAh g(-1)). The composite also demonstrates high specific discharge capacities at different current rates (1318, 1032, 661, and 460 mAh g(-1) at 0.5, 1.0, 2.0, and 4.0 C, respectively). The superior electrochemical performance of Ge-polypyrrole composite could be attributed to the polypyrrole core, which provides an efficient transport pathway for electrons. SEM images of the electrodes have demonstrated that polypyrrole can also act as a conductive binder and alleviate the pulverization of electrode caused by the huge volume changes of the nanosized germanium particles during Li(+) intercalation/de-intercalation.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148674 | PMC |
http://dx.doi.org/10.1038/srep06095 | DOI Listing |
Adv Sci (Weinh)
January 2025
Joint Key Laboratory of the Ministry of Education, Institute of Applied Physics and Materials Engineering, University of Macau, Avenida da Universidade, Taipa, Macau SAR, 999078, China.
Potassium-sulfur (K-S) batteries are severely limited by the sluggish reaction kinetics of the cyclooctasulfur (cyclo-S) electrode with low conductivity, which urgently requires a novel cathode to facilitate activity to improve sulfur utilization. In this study, using the wet chemistry method, the molecular clip of Li is created to replace cyclo-S molecular with the highly active chain-like S molecular. The molecular clip strategy effectively lowers the reaction barrier in potassium-sulfur systems, and the stretching of S─S bonds weakens the binding between sulfur atoms, facilitating the transformation of potassium polysulfides (KPSs).
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Graduate School of Human and Environmental Studies, Kyoto University, Sakyo, Kyoto 606-8501, Japan.
All-solid-state fluoride-ion batteries (FIBs) have attracted extensive attention as candidates for next-generation energy storage devices; however, promising cathodes with high energy density are still lacking. In this study, CuN is investigated as a cathode material for all-solid-state fluoride-ion batteries, which offers enough anionic vacancies around the 2-fold coordinated Cu center for F intercalation, thereby enabling a multielectron-transferred fluorination process. The contribution of both cationic and anionic redox to charge compensation, in particular, the generation of molecular nitrogen species in highly charged states, has been proved by several synchrotron-radiation-based spectroscopic technologies.
View Article and Find Full Text PDFNano Lett
January 2025
Department of Chemistry, Fudan University, Shanghai 200433, China.
Vanadium-based oxides have garnered significant attention for aqueous zinc batteries (AZBs), whereas sluggish Zn diffusion and structural collapse remain major challenges in achieving high-performance cathodes. Herein, different structures of iron-vanadium oxides were fabricated by modulating the amount of vanadium content. It is found that the porous Mott-Schottky heterojunction composed of FeVO and FeVO mixed phase was used to construct a self-generated FeVO-5 structure, which could lower the diffusion barrier and improve the electron transport derived from the formed built-in electric field at the interface, showing faster reaction kinetics and improved capacity compared with the singe-phase FeVO-1.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
School of Materials Science and Engineering, State Key Laboratory of Fine Chemicals, Frontiers Science Center for Smart Materials Oriented Chemical Engineering, Technology Innovation Center of High Performance Resin Materials (Liaoning Province), Dalian University of Technology, Dalian, 116024, China.
Sodium-metal batteries (SMBs) using solid-state polymer electrolytes (SPEs) show impressive superiority in energy density and safety. As promising candidates for SPEs, solid-state plastic crystal electrolytes (SPCE) based on succinonitrile (SN) plastic crystal could achieve high ion conductivity and wide voltage window. Nonetheless, the notorious SN decomposition reaction on the electrode/electrolyte interface seriously challenges the stable operation of the battery.
View Article and Find Full Text PDFAdv Mater
January 2025
School of Physics and Electronics, Hunan University, Changsha, 410082, P. R. China.
Single-electron transfer, low alkali metal contents, and large-molecular masses limit the capacity of cathodes. This study uses a cost-effective and light-molecular-mass orthosilicate material, KFeSiO, with a high initial potassium content, as a cathode for potassium-ion batteries to enable the transfer of more than one electron. Despite the limited valence change of Fe ions during cycling, KFeSiO can undergo multiple electron transfers via successive oxygen anionic redox reactions to generate a high reversible capacity.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!