ترغب بنشر مسار تعليمي؟ اضغط هنا

In Operando magnetometry study on the charge storage mechanism of SnCo alloy lithium ion batteries

144   0   0.0 ( 0 )
 نشر من قبل Qingtao Xia
 تاريخ النشر 2021
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

In view of the long-standing controversy over the reversibility of transition metals in Sn-based alloys as anode for Li-ion batteries, an in situ real-time magnetic monitoring method was used to investigate the evolution of Sn-Co intermetallic during the electrochemical cycling. Sn-Co alloy film anodes with different compositions were prepared via magnetron sputtering without using binders and conductive additives. The magnetic responses showed that the Co particles liberated by Li insertion recombine fully with Sn during the delithiation to reform Sn-Co intermetallic into stannum richer phases Sn7Co3. However, as the Co content increases, it can only recombine partially with Sn into cobalt richer phases Sn3Co7. The unconverted Co particles may form a dense barrier layer and prevent the full reaction of Li with all the Sn in the anode, leading to lower capacities. These critical results shed light on understanding the reaction mechanism of transition metals, and provide valuable insights toward the design of high-performance Sn alloy based anodes.

قيم البحث

اقرأ أيضاً

Non-destructive determination of lithium distribution in a working battery is key for addressing both efficiency and safety issues. Although various techniques have been developed to map the lithium distribution in electrodes, these methods are mostl y applicable to test cells. Here we propose the use of high-energy x-ray Compton scattering spectroscopy to measure the local lithium concentration in closed electrochemical cells. A combination of experimental measurements and parallel first-principles computations is used to show that the shape parameter S of the Compton profile is linearly proportional to lithium concentration and thus provides a viable descriptor for this important quantity. The merits and applicability of our method are demonstrated with illustrative examples of LixMn2O4 cathodes and a working commercial lithium coin battery CR2032.
A thick electrode with high areal capacity has been developed as a strategy for high-energy-density lithium-ion batteries, but thick electrodes have difficulties in manufacturing and limitations in ion transport. Here, we reported a new manufacturing approach for ultra-thick electrode with aligned structure, called structure electrode additive manufacturing or SEAM, which aligns active materials to the through-thicknesses direction of electrodes using shear flow and a designed printing path. The ultra-thick electrodes with high loading of active materials, low tortuous structure, and good structure stability resulting from a simple and scalable SEAM lead to rapid ion transport and fast electrolyte infusion, delivering a higher areal capacity than slurry-casted thick electrodes. SEAM shows strengths in design flexibility and scalability, which allows the production of practical high energy/power density structure electrodes.
214 - Yang He , Meng Gu , Haiyan Xiao 2015
Conversion reaction is one of the most important chemical processes in energy storage such as lithium ion batteries. While it is generally assumed that the conversion reaction is initiated by ion intercalation into the electrode material, solid evide nce of intercalation and the subsequent transition mechanism to conversion remain elusive. Here, using well-defined WO3 single crystalline thin films grown on Nb doped SrTiO3(001) as a model electrode, we elucidate the conversion reaction mechanisms during Li+, Na+ and Ca2+ insertion into WO3 by in situ transmission electron microscopy studies. Intercalation reactions are explicitly revealed for all ion insertions. With corroboration from first principle molecular simulations, it is found that, beyond intercalation, ion-oxygen bonding destabilize the W framework, which gradually collapses to pseudo-amorphous structure. In addition, we show the interfacial tensile strain imposed by the SrTiO3 substrate can preserve the structure of an ultra-thin layer of WO3, offering a possible engineering solution to improve the cyclability of electrode materials. This study provides a detailed atomistic picture on the conversion-type electrodes in secondary ion batteries.
Using first principles structure searching with density-functional theory (DFT) we identify a novel $Fmbar{3}m$ phase of Cu$_2$P and two low-lying metastable structures, an $Ibar{4}3d$--Cu$_3$P phase, and a $Cm$--Cu$_3$P$_{11}$ phase. The computed pa ir distribution function of the novel $Cm$--Cu$_3$P$_{11}$ phase shows its structural similarity to the experimentally identified $Cm$--Cu$_2$P$_7$ phase. The relative stability of all Cu--P phases at finite temperatures is determined by calculating the Gibbs free energy using vibrational effects from phonon modes at 0 K. From this, a finite-temperature convex hull is created, on which $Fmbar{3}m$--Cu$_2$P is dynamically stable and the Cu$_{3-x}$P ($x < 1$) defect phase $Cmc2_1$--Cu$_8$P$_3$ remains metastable (within 20 meV/atom of the convex hull) across a temperature range from 0 K to 600 K. Both CuP$_2$ and Cu$_3$P exhibit theoretical gravimetric capacities higher than contemporary graphite anodes for Li-ion batteries; the predicted Cu$_2$P phase has a theoretical gravimetric capacity of 508 mAh/g as a Li-ion battery electrode, greater than both Cu$_3$P (363 mAh/g) and graphite (372 mAh/g). Cu$_2$P is also predicted to be both non-magnetic and metallic, which should promote efficient electron transfer in the anode. Cu$_2$Ps favorable properties as a metallic, high-capacity material suggest its use as a future conversion anode for Li-ion batteries; with a volume expansion of 99% during complete cycling, Cu$_2$P anodes could be more durable than other conversion anodes in the Cu--P system with volume expansions greater than 150%.
Crystal structures play a vital role in determining materials properties. In Li-ion cathodes, the crystal structure defines the dimensionality and connectivity of interstitial sites, thus determining Li-ion diffusion kinetics. While a perfect crystal has infinite structural coherence, a class of recently discovered high-capacity cathodes, Li-excess cation-disordered rocksalts, falls on the other end of the spectrum: Their cation sublattices are assumed to be randomly populated by Li and transition metal ions with zero configurational coherence based on conventional X-ray diffraction, such that the Li transport is purely determined by statistical effects. In contrast to this prevailing view, we reveal that cation short-range order, hidden in diffraction, is ubiquitous in these long-range disordered materials and controls the local and macroscopic environments for Li-ion transport. Our work not only discovers a crucial property that has previously been overlooked, but also provides new guidelines for designing and engineering disordered rocksalts cathode materials.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا