The grown demand of current and future development of new technologies for high added value and strategic metals, such as molybdenum, vanadium, and chromium, and facing to the depletion of basic primary resources of these metals, the metal extraction and recovery from industrial by-products and wastes is a promising choice. Slag from the steelmaking sector contains a significant amount of metals; therefore, it must be considered to be an abundant secondary resource for several strategic materials, especially chromium. In this work, the generated slag from electric arc furnace (EAF) provided by the French steel industry was characterized by using multitude analytical techniques in order to determine the physico-chemical characteristics of the targeted slag. The revealed main crystallized phases are larnite (Ca2SiO4), magnetite (Fe3O4), srebrodolskite (Ca2Fe2O5), wüstite (FeO), maghemite (Fe2.6O3), hematite (Fe2O3), chromite [(Fe,Mg)Cr2O4], and quartz (SiO2). The collected slag sample contains about 34.1% iron (48.5% Fe2O3) and 3.5% chromium, whilst the vanadium contents is around 1500 ppm. The Mössbauer spectroscopy suggested that the non-magnetic fraction represents 42 wt% of the slag, while the remainder (58 wt%) is composed of magnetic components. The thermal treatment of steel slag up to 900 °C indicated that this solid is almost stable and few contained phases change their structures.
Silicon is attractive as negative electrode material for Li-ion batteries (LIBs) to increase their energy density [1]. The main challenge is to deal with the large silicon volume expansion induced by its lithiation, which damages the mechanical integrity of the electrode, and produces an unstable solid electrolyte interphase (SEI). Recently, we have discovered a post-processing treatment, called maturation, which very significantly improves the mechanical and electrochemical stabilities of silicon-based electrodes made with polycarboxylic acid binders [2-4]. It consists of storing the electrode in a humid atmosphere for a few days before drying and cell assembly. We found that during maturation, the atmospheric-induced corrosion of the current collector releases oxidized copper species that migrate into the electrode to physically crosslink the binder phase, substantially modifying its resiliency to the silicon volume variation as shown by various in situ and operando characterizations. The pre-addition of a small amount of copper or zinc salt in the electrode slurry allows to reach similar improvement of electrochemical performance than maturation [5]. This reveals that there is great potential to explore coordination chemistry to design new, more efficient binders through the medium strength and dynamic nature of coordination bonds [6]. Acknowledgments The authors thank the Natural Sciences and Engineering Research Council of Canada (NSERC) (grant RGPIN-2016-04524) and Transition Énergétique Québec (TEQ) (grant Techno-0040-0001) for financial support of this work. References [1] M.N. Obrovac, Si-alloy negative electrodes for Li-ion batteries. Current Opinion in Electrochemistr, 2018, 9, 8–17. [2] Z. Karkar et al., How silicon electrodes can be calendered without altering their mechanical strength and cycle life J. Power Sources, 2017, 371, 136-147. [3] C. Real Hernandez et al., A Facile and Very Effective Method to Enhance the Mechanical Strength and the Cyclability of Si-Based Electrodes for Li-Ion Batteries, Adv. Energy Mater, 2017, 1701787. [4] V. Vanpenne et al., Adv. Energy Mater, Dynamics of the morphological degradation of Si-based anodes for Li-ion batteries characterized by in-situ synchrotron X-ray tomography, Adv. Energy Mater. 9, 2019, 1803947 [5] D. Mazouzi et al., CMC-citric acid Cu(II) cross-linked binder approach to improve the electrochemical performance of Si-based electrodes Electrochimica Acta, 2019, 304, 495-504. [6] T. Devic, B. Lestriez, L. Roué, Silicon Electrodes for Li-Ion Batteries. Addressing the Challenges through Coordination Chemistry, ACS Energy Letters, ACS Energy Lett., 2019, 4, 550−557.
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