Owing to the desirable nano-morphology, controllable structure, and ease of preparation, metal-organic frameworks (MOFs) are widely used as the precursors for electrodes in Na-ion battery (NIB). However, MOF structures are prone to fracture and collapse during the reactions. Additionally, MOF-derived electrodes often exhibit a high expansion rate, which negatively impacts the long cyclic capability of NIBs. Herein, we employed a stable covalent-organic framework (COF) as a protective coating for the first time to preserve the MOF structure. A shuttle-like iron selenide (FeSe) coated with N-doped carbon (NC) was synthesized using a simple hydrothermal method, surface coating, and subsequent selenizing process. Due to its large specific surface area and well-developed porosity, the double-framework derived FeSe/NC electrode provides abundant active sites for Na storage. The COF and COF-derived NC protect the structure of FeSe/NC during synthesis and cyclic process, respectively. The high conductivity of the NC coating enhances the electron/ion conductivity of FeSe/NC, thereby beneficial the rate performance. As the material anode for NIB, the FeSe/NC electrode exhibits a high initial charging/discharging capacity (425.7/478.4 mAh·g with an initial Coulombic efficiency of 89.0 %), excellent rate performance (333.5 mAh·g at 12 A·g), long-durable cycle capability (290.8 mAh·g after 1000 cycles at 8 A·g) and fast charging ability (143 s). This work provides a novel strategy of "COF on MOF" to prepare high-performance electrode materials for NIB.
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http://dx.doi.org/10.1016/j.jcis.2023.07.126 | DOI Listing |
Organometallics
January 2025
School of Chemical Sciences, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States.
The dianion [Fe[(μ-SeCH)NH](CN)(CO)] ([]) is of interest for the preparation of the selenide analog of the active site of the [FeFe]-hydrogenases. The obvious route for its synthesis by cyanation of Fe[(μ-SeCH)NH](CO) () fails for reasons that this paper explains and resolves. We show that CN cleaves Se-C bonds in .
View Article and Find Full Text PDFSmall
December 2024
Institute of Photoelectronic Thin Film Devices and Technology, Renewable Energy Conversion and Storage Center, State Key Laboratory of Photovoltaic Materials and Cells, Nankai University, Tianjin, 300350, P. R. China.
Photovoltaic-driven electrochemical (PV-EC) carbon dioxide reduction (COR) coupled with sulfide oxidation (SOR) can efficiently convert the solar energy into chemical energy, expanding its applications. However, developing low-cost electrocatalysts that exhibit high selectivity and efficiency for both COR and SOR remains a challenge. Herein, a bifunctional copper selenide catalyst is developed with copper vacancies (v-CuSe) for the COR-SOR.
View Article and Find Full Text PDFInorg Chem
December 2024
Department Chemie, Ludwig-Maximilians-Universität München, Butenandtstr. 9-13 (D), 81377 München, Germany.
[Na(HO)][FeSe] was synthesized using hydrothermal methods and characterized by single-crystal X-ray diffraction, Fe Mössbauer spectroscopy, magnetization, and muon spin resonance (μSR) measurements. The cubic crystal structure (space group 23, = 11.785 Å, = 2) contains heterocubane-type clusters with symmetry.
View Article and Find Full Text PDFJ Colloid Interface Sci
March 2025
School of Chemistry and Chemical Engineering, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, China. Electronic address:
Controlled synthesis of hierarchical flowerlike cobalt tin sulfide (SnCoS) is successfully obtained using the chelation of the biomolecule l-asparagine with cobalt-tin metal cations by a hydrothermal technique. l-asparagine plays a crucial role as an inducer and a good structure-directing activity. Subsequently, pine needle-shaped cobalt iron selenium (FeCoSe) is tightly deposited on the SnCoS surface to construct cobalt tin sulfide coated with cobalt iron selenide (FeCoSe@SnCoS) heterostructure, which has exposed more active sites and the most abundant channels for electron/ion transfer.
View Article and Find Full Text PDFJ Fluoresc
November 2024
University of Maryland Baltimore County, 1000 Hilltop Circle, Baltimore, MD, 21250, USA.
Zinc selenide is an excellent matrix material to dope with rare-earth and transition metal to achieve mid-infrared luminescence to develop high power lasers. The luminescence, morphology and refractive index is significantly affected by the doping and defects generated due to size and valency of dopants, concentration, growth process and convection during the growth. The aim of the study is to investigate effect of point and line defects generated due to low doping of iron and chromium on the emission and morphology of the zinc selenide.
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