Mitigating First Year Burnout: How Reimagined Partnerships Could Support Urban Middle Level Teachers

Given what we know about new teacher attrition—most teachers leave within their first five years in the field—specialized support during early years of teaching is critical. But should this support look different across different contexts and grade bands? What does supportive teacher education and induction look like for middle level educators preparing to teach in urban settings? This essay describes steps taken to design a cross-institutional, collaborative 3-year residency program for K-8 educators, and speaks to the importance of reimagined co-teaching, critical, and cross-institutional partnerships in middle grades teacher education. The authors urge readers to consider how to implement similar modifications in their own spaces to create powerful, collaborative middle grades teacher education and induction

High Flux Femtosecond X-ray Emission from the Electron-Hose Instability in Laser Wakefield Accelerators

Bright and ultrashort duration X-ray pulses can be produced by through betatron oscillations of electrons during Laser Wakefield Acceleration (LWFA). Our experimental measurements using the \textsc{Hercules} laser system demonstrate a dramatic increase in X-ray flux for interaction distances beyond the depletion/dephasing lengths, where the initial electron bunch injected into the first wake bucket catches up with the laser pulse front and the laser pulse depletes. A transition from an LWFA regime to a beam-driven plasma wakefield acceleration (PWFA) regime consequently occurs. The drive electron bunch is susceptible to the electron-hose instability and rapidly develops large amplitude oscillations in its tail, which leads to greatly enhanced X-ray radiation emission. We measure the X-ray flux as a function of acceleration length using a variable length gas cell. 3D particle-in-cell (PIC) simulations using a Monte Carlo synchrotron X-ray emission algorithm elucidate the time-dependent variations in the radiation emission processes.Comment: 6 pages, 4 figures, accepted for publication in Phys. Rev. Accel. Beam

Solvent-Dictated Sodium Sulfur Redox Reactions: Investigation of Carbonate and Ether Electrolytes

Sulfur-based cathode chemistries are essential for the development of high energy density alkali-ion batteries. Here, we elucidate the redox kinetics of sulfur confined on carbon nanotubes, comparing its performance in ether-based and carbonate-based electrolytes at room temperature. The solvent is found to play a key role for the electrochemical reactivity of the sulfur cathode in sodium–sulfur (Na–S) batteries. Ether-based electrolytes contribute to a more complete reduction of sulfur and enable a higher electrochemical reversibility. On the other hand, an irreversible solution-phase reaction is observed in carbonate solvents. This study clearly reveals the solvent-dependent Na–S reaction pathways in room temperature Na–S batteries and provides an insight into realizing their high energy potential, via electrolyte formulation design

Fast kinetics of multivalent intercalation chemistry enabled by solvated magnesium-ions into self-established metallic layered materials

Rechargeable magnesium batteries are one of the most promising candidates for next-generation battery technologies. Despite recent significant progress in the development of efficient electrolytes, an on-going challenge for realization of rechargeable magnesium batteries remains to overcome the sluggish kinetics caused by the strong interaction between double charged magnesium-ions and the intercalation host. Herein, we report that a magnesium battery chemistry with fast intercalation kinetics in the layered molybdenum disulfide structures can be enabled by using solvated magnesium-ions ([Mg(DME)x]2+). Our study demonstrates that the high charge density of magnesium-ion may be mitigated through dimethoxyethane solvation, which avoids the sluggish desolvation process at the cathode-electrolyte interfaces and reduces the trapping force of the cathode lattice to the cations, facilitating magnesium-ion diffusion. The concept of using solvation effect could be a general and effective route to tackle the sluggish intercalation kinetics of magnesium-ions, which can potentially be extended to other host structures

Embedding Heterostructured α‐MnS/MnO Nanoparticles in S‐Doped Carbonaceous Porous Framework as High‐Performance Anode for Lithium‐Ion Batteries

In this work, the synthesis of α-MnS/MnO/S-doped C micro-rod composites via a simple sulfidation process is demonstrated, starting from a Mn-based metal-organic framework. The resulting heterostructured α-MnS/MnO nanoparticles (8±2 nm) are uniformly embedded into the S-doped carbonaceous porous framework with hierarchical micro-/meso-porosity. The combination of structural and compositional characteristics results in the promising electrochemical performance of the as-obtained composites as anode materials for lithium-ion batteries, coupled with high reversible capacity (940 mAh $g^{−1}$ at 0.1 A $g^{−1}$), excellent rate capability as well as long cycling lifespan at high rate of 2.0 A $g^{−1}$ for 2000 cycles with the eventual capacity of ∼300 mAh $g^{−1}$. Importantly, in situ X-ray diffraction studies clearly reveal mechanistic details of the lithium storage mechanism, involving multistep conversion processes upon initial lithiation

Model Studies on Solid Electrolyte Interphase Formation on Graphite Electrodes in Ethylene Carbonate and Dimethyl Carbonate II: Graphite Powder Electrodes

As part of a systematic study on the formation and composition of the solid electrolyte interphase (SEI) in lithium‐ion batteries (LIBs), going stepwise from highly idealized electrodes such as highly oriented pyrolytic graphite and conditions such as ultrahigh vacuum conditions to more realistic materials and reaction conditions, we investigated the decomposition of simplified electrolytes (ethylene carbonate (EC)+1 M LiPF$_{6}$ and dimethyl carbonate (DMC)+1 M LiPF$_{6}$) at binder‐free graphite powder model electrodes. The results obtained from cyclic voltammetry and ex situ X‐ray photoelectron spectroscopy half‐cell measurements – in particular on the effect of cycling rate, solvent and electrode – are explained in terms of a mechanistic model where electrolyte decomposition occurs at the SEI | electrode interface and where transport of solvent and salt species through the growing SEI plays an important role for explaining the observed change from preferential salt decomposition to solvent decomposition with increasing cycling rate

Reversible Copper Sulfide Conversion in Nonflammable Trimethyl Phosphate Electrolytes for Safe Sodium‐Ion Batteries

Rechargeable sodium-ion batteries are considered promising candidates for low-cost and large-scale energy storage systems. However, the limited energy density, cyclability, and safety issues remain challenges for practical applications. Herein, investigation of the Cu1.8S/C composite material as the negative electrode active (conversion) material in combination with a concentrated electrolyte composed of a 3.3 m solution of sodium bis(fluorosulfonyl)imide (NaFSI) in trymethyl phosphate and fluoroethylene carbonate (FEC) as the additive is reported on. Such a combination enables the stable cycling of the conversion-type Cu1.8S/C electrode material for hundreds of cycles with high capacity (380 mAh g−1). Both the salt (NaFSI) and the additive (FEC) contribute to the formation of a stable NaF-rich solid electrolyte interphase (SEI) on the anode surface. A full cell using the Na3V2(PO4)3/C cathode also demonstrates stable cycling performance for 200 cycles with a promising Coulombic efficiency (CE) (99.3%). These findings open new opportunities for the development of safer rechargeable sodium-ion batteries