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At least 1,531 records · Page 85

Origin of Electrochemical Activation Leading to Enhanced Cycling Stability of Li‐ and Mn‐Rich Cathodes

Electrochemical activation is a critical step for optimal functioning of Li- and Mn-rich (LMR) cathodes, yet the underlying mechanism for such activation remains elusive. Here, by using scanning/transmission electron microscopy (S/TEM) combined with the associated energy-dispersive x-ray spectroscopy (EDS) and electron energy-loss spectroscopy (EELS), we decipher the origin of the activation enhanced electrochemical properties. We reveal that activation induces the formation of a spinel-like phase within the C2/m domains of the LMR cathode, where the transition-metal ions partially occupy both the tetrahedral (8a) and octahedral (16c) sites of the $Fd\bar{3}m$ spinel lattice, distinguishing the spinel-like phase from the conventional high-voltage spinel. Systematic varying the cycling voltage reveals a critical activation voltage above which this spinel-like phase forms, while lower voltages preserve the layered bulk structure. As the spinel-like phase is a stable structure for electrochemical cycling, the present findings provide direct mechanistic insight into the voltage-dependent activation process and explain how the C2/m to spinel-like transformation upon activation contributes to the electrochemical performance of LMR cathodes, providing guidance for the rational design of Li-rich cathodes with enhanced cycling durability.

Li-rich and Mn-rich cathode↗

TiN‐Au/HfO 2 ‐Au Multilayer Thin Films with Tunable Hyperbolic Optical Response

Abstract Hyperbolic metamaterials (HMM) possess significant anisotropic physical properties and tunability and thus find many applications in integrated photonic devices. HMMs consisting of metal and dielectric phases in either multilayer or vertically aligned nanocomposites (VAN) form are demonstrated with different hyperbolic properties. Herein, self‐assembled HfO 2 ‐Au/TiN‐Au multilayer thin films, combining both the multilayer and VAN designs, are demonstrated. Specifically, Au nanopillars embedded in HfO 2 and TiN layers forming the alternative layers of HfO 2 ‐Au VAN and TiN‐Au VAN. The HfO 2 and TiN layer thickness is carefully controlled by varying laser pulses during pulsed laser deposition (PLD). Interestingly, tunable anisotropic physical properties can be achieved by adjusting the bi‐layer thickness and the number of the bi‐layers. Type II optical hyperbolic dispersion can be obtained from high layer thickness structure (e.g., 20 nm), while it can be transformed into Type I optical hyperbolic dispersion by reducing the thickness to a proper value (e.g., 4 nm). This new nanoscale hybrid metamaterial structure with the three‐phase VAN design shows great potential for tailorable optical components in future integrated devices.

Chemistry↗

Planar optical waveguide for refractive index determining with high sensitivity and dual-band characteristic for Nano-sensor application

In this paper, we develop an optical waveguide based on metal–insulator-metal as a refractive index sensor with dual-band feature and a high figure of merit (FOM) and sensitivity. In this model, we utilize a Z-shape slot based on two stubs model in both metal layers and this structure is placed over a dielectric layer of SiO{sub 2} as a substrate for planar application in the optical systems. In addition, the parametric studies are used to clarifying the elements influence on controlling the transmission and working frequency to achieve a dual-band characteristic at 1550 and 3100 nm which is suitable for optical fiber application. In fact, the compound stubs technique is suggested to modify the resonances of the waveguide for dual-band attributes based on the transmission line model. We simulate this waveguide using the Finite Integrated Technique (FIT) method. It is supposed that the waveguide is filled by various materials with the different refractive indexes in the range of 1 to 1.5. We obtain the FOM for these materials while the Fano response provides high FOM about the 3800 RIU{sup −1} and the sensitivity is 1790 nm/RIU. Therefore, the compound stubs strategy help to improve the FOM factor in the optical waveguide.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Characterization and recovery of rare earth elements and other critical metals (Co, Cr, Li, Mn, Sr, and V) from the calcination products of a coal refuse sample

Here, the impacts of calcination on the leaching recovery of rare earth elements (REEs) and other critical metals from a Baker seam coal refuse material were investigated. Acid leaching test results showed that leaching recovery of the REEs, especially the light REEs, was increased significantly from around 24% to 80–90% after calcination under 600–750 °C for two hours. By considering the major element leaching kinetics and the mineralogical changes of the dominant minerals caused by calcination, two mechanisms were proposed for the improved leaching performance: (1) decomposition of difficult-to-dissolve REE-bearing minerals into soluble forms; and (2) liberation of REE-bearing minerals encapsulated in clays after calcination due to the dehydration and disintegration of the layered clay structure. Sequential chemical extraction tests showed that a significant fraction (around 75%) of the REEs in the raw material were present in an insoluble form. After calcination under proper temperatures (600–800 °C), the majority of the insoluble light REEs (LREEs) were converted into soluble forms. Changes in the modes of occurrence of the LREEs and phosphorous based on leaching rate and sequential leaching correlated well as a function of the calcination temperature. This finding in addition to SEM-EDX results tends to indicate the potential that the LREEs occur primarily as rare earth phosphates such as monazite in the untreated coal refuse material. The acid leaching and sequential chemical extraction results show that co-extraction of REEs and other critical metals such as Co, Mn, and Li is possible using a calcination-acid leaching procedure.

01 COAL, LIGNITE, AND PEAT↗

High-Performance Thermoelectrics from Cellular Nanostructured Sb 2 Si 2 Te 6

We introduce Sb 2 Si 2 Te 6 as a high-performance thermoelectric material. Single-crystal X-ray diffraction analysis indicates that Sb 2 Si 2 Te 6 has a layered twodimensional structure with Sb 3+ cations and [Si 2 Te 6 ] 6- units as building blocks adopting the Fe 2 P 2 Se 6 structure type. Sb 2 Si 2 Te 6 is a direct-band-gap semiconductor with valence-band maximum and conduction-band minimum at the Z point in the Brillouin zone, where the band is doubly degenerate. Polycrystalline bulk pellets of Sb 2 Si 2 Te 6 with randomly packed grains exhibit an intrinsically high thermoelectric figure of merit ZT of ~1.08 at 823 K. We then create a cellular nanostructure with ultrathin Si 2 Te 3 nanosheets covering the Sb 2 Si 2 Te 6 grains, which act as a hole-transmitting electron-blocking filter and at the same time cause extra phonon scattering. Lastly, this dual function of the cellular nanostructure achieves an ultralow thermal conductivity value of ~0.29 Wm -1 K -1 and a high ZT value of ~1.65 at 823 K for Sb 2 Si 2 Te 6 , along with a high average ZT value of ~0.98.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Multi-technique characterization of spray coated and roll-to-roll coated gas diffusion fuel cell electrodes

Here this work reports the characterization of catalyst layer (CL) structure and composition for a set of gas-diffusion electrodes (GDEs) fabricated by different coating methods with the goal of developing a better understanding of CL processing-structure-property-performance relationships. The CL coating techniques used in this study were ultrasonic spray coating, and two roll-to-roll (R2R) methods - gravure and slot die. Scanning transmission electron microscopy (STEM) coupled with X-ray energy dispersive spectroscopy (EDS) analysis of GDE cross-sections provided bulk information, while scanning electron microscopy (SEM) with EDS and X-ray photoelectron spectroscopy (XPS) were used to investigate the near surface and surface composition of the CLs that will be in direct contact with the membrane once the membrane electrode assembly (MEA) is constructed. This study demonstrates that common quantification parameters, namely the F:Pt ratio extracted from cross-sectional STEM-EDS maps and top-down CL measurements with SEM and XPS, along with roughness parameters quantified from SEM micrographs are useful parameters in explaining and potentially predicting performance trends. Additionally, it highlights the importance of understanding key CL surface properties for advancing the manufacturability of high-performance components for polymer electrolyte membrane (PEM) technologies.

30 DIRECT ENERGY CONVERSION↗

The role of frequency on fretting corrosion of Alloy 690TT against 304 stainless steel in high temperature high pressure water

Highlights: • Delamination, material transfer and oxidation dominated fretting corrosion behavior in HTHP water. • Delamination was pure mechanical wear to produce fresh surface exposed to HTHP water for oxidation. • Increased frequency enhanced the maximum thickness of oxide film in worn surface. • Increased frequency accelerated the formation of tribologically transformed structure (TTS). • Increased frequency accelerated the escape of wear debris, which originated from the TTS and crushed oxide particles. - Abstract: In high temperature high pressure (HTHP) water, the role of frequency in fretting corrosion behavior and mechanism of Alloy 690TT against Type 304 stainless steel were investigated. Results indicated that wear mechanisms of delamination, material transfer and oxidation collectively dominated the fretting corrosion behavior. The delamination was related to pure mechanical wear to produce fresh surface exposed to HTHP water for oxidation, resulting in the increase of wear depth and volume. The increasing frequency played little role in oxide type of worn surfaces, which consisted of (Ni,Fe)(Fe,Cr){sub 2}O{sub 4} and Cr{sub 2}O{sub 3}. However, it enhanced the maximum thickness of oxide film in the worn surface. The increasing frequency resulted in the acceleration of the formation of nanostructured tribologically transformed structure (TTS) layer because it could aggravate the plastic deformation and increase the contact temperature for dynamic recrystallization. The increasing frequency accelerated the escape of the ultra-fine grained wear debris, which originated from not only the damage of TTS layer but also the crushed oxide particles generated in the contact gap.

36 MATERIALS SCIENCE↗

Layered Li{sub 1+x}(Ni{sub 0.33}Co{sub 0.33}Mn{sub 0.33})O{sub 2} cathode material prepared by microwave assisted solvothermal method for lithium ion batteries

Highlights: • Microwave assisted solvothermal method. • Effect of (0.05–0.2) mol% of excess lithium in layered Li{sub 1+x}(Ni{sub 0.33}Co{sub 0.33}Mn{sub 0.33})O{sub 2}. • Different calcination temperature. • Voltage-cut off optimization. • Conductivity and electrochemical performance correlation. - Abstract: Layered hexagonal structure Li{sub 1+x}(Ni{sub 0.33}Co{sub 0.33}Mn{sub 0.33})O{sub 2} (LNCM) (x = 0, 0.05, 0.1, 0.15 and 0.2 mol%) compounds were prepared by microwave assisted solvothermal method at two different calcination temperature of 850 and 950 °C. The phase purity of the LNCM compounds was confirmed by Rietveld refined XRD pattern, Raman, and HRTEM studies. The average particle sizes were in the submicron range as confirmed by SEM and TEM analysis. Galvanostatic cycling studies were made in various voltage range, 2.5 to 4.4/4.6/4.8 V at a current rate of 0.2 C. Among all the compounds, LNCM prepared at 950 °C (HS3) exhibited an initial discharge capacity of 197 mAh/g and maintained a capacity of 180 mAh/g at the end of 40{sup th} cycle in 2.5–4.6 V window, indicating an excellent capacity retention. HS3 shows the electrical conductivity of 9.31 × 10{sup −6} S/cm, which was higher than all the other compounds and discussed the reason for the improved electrochemical performance.

36 MATERIALS SCIENCE↗

Petaloid-shaped ZnO coated carbon felt as a controllable host to construct hierarchical Li composite anode

Prestoring Li metal into the 3D host via thermal infusion strategy has been considered as an effective approach on suppressing Li dendrites growth of Li-metal anode during cycling. However, the fast Li infusing process generally induces uncontrollable and undesirable structures during the formation of composite Li metal anode. It is widely accepted that both physical and chemical interactions between the molten Li and the hosts provide driving forces for Li infusing into the host, but which one plays the dominant role has not been explored clearly. In this work, a 3D carbon felt coated by petaloid zinc oxide (CFZO) is designed as a controllable host for prestoring Li metal via thermal infusion method. It is revealed that the morphology induced physical driving force plays a more important role than the chemical reaction between ZnO and molten Li in the thermal infusion process. The physical driving force originates from the capillarity effect, depending on the roughness of the host according to Wenzel's model. An adjustable Li infusing process can be controlled to fabricate the Li composite electrode with a hierarchical structure (with dense Li-rich layer and porous Li-poor layer). The unique structure of the CFZO-Li not only provides enough spaces for Li deposition, but also disperses local current density to induce a uniform Li deposition behavior, thus Li dendrites can be suppressed effectively. As a result, CFZO-Li anode exhibits promising cycle stability when coupled with both Li-containing (LiNi 0.8 Co 0.15 Al 0.05 O 2 ) and Li-free (sulfur) cathodes.

25 ENERGY STORAGE↗

Flexible all-organic nanocomposite films interlayered with in situ synthesized covalent organic frameworks for electrostatic energy storage

Poly(vinylidene fluoride)-based terpolymers, known for having the largest dielectric constant among the existing dielectric polymers, are attractive materials for electrostatic film capacitors used in lightweight electrification systems. However, the potential of these terpolymers in film capacitor applications remains constrained by their low electrical insulating and mechanical strengths. To address these limitations, we introduced rigid covalent organic framework (COF) nanospheres into the thin films of soft terpolymers via in situ synthesis and a facile layer-by-layer solution casting method, whereby multilayer films consisting of two polymer outer layers and a COF-containing middle layer were readily obtained. The resultant all-organic thin films exhibit simultaneously high dielectric constant, enhanced breakdown strength, superior energy density (~25 J cm –3 ) at efficiencies over 80%, along with greatly improved mechanical self-supporting capability and excellent mechanical flexibility. Here, this work demonstrates the unprecedented use of COF for electrostatic energy storage, uncovering its potential for flexible electronic applications operating under high electric fields.

25 ENERGY STORAGE↗

A box model for representing estuarine physical processes in Earth system models

Appropriately treating riverine freshwater discharge into the oceans in Earth system models is a challenging problem. Commonly, the river runoff is discharged into the ocean models with zero salinity and arbitrarily distributed either horizontally or vertically over several grid cells. Those approaches entirely neglect estuarine physical processes that modify river inputs before they reach the open ocean. Here in order to realistically represent riverine freshwater inputs in Earth system models, a physically based Estuary Box Model (EBM) is developed to parameterize the mixing processes in estuaries. The EBM represents the estuary exchange circulation with a two-layer box structure. It takes as input the river volume flux from the land surface model and the subsurface salinity at the estuary mouth from the ocean model. It delivers the estuarine outflow salinity and net volume flux into and out of the estuary to the ocean model. An offline test of the EBM forced with observed conditions for the Columbia River system shows good agreement with observations of outflow salinity and high-resolution simulations of the exchange flow volume flux. To illustrate the practicality of use of the EBM in an Earth system model, the EBM is implemented for all coastal grid cells with river runoff in the Community Earth System Model (CESM). Compared to the standard version of CESM, which treats runoff as an augmentation to precipitation, the EBM increases sea surface salinity and reduces stratification near river mouths. The EBM also leads to significant regional and remote changes in CESM ocean surface salinities.

54 ENVIRONMENTAL SCIENCES↗

Single-Crystal Synthesis and Characterization of Copper-Intercalated ZrTe 5

Herein is presented the synthesis and characterization of copper-intercalated zirconium pentatelluride (ZrTe 5 ). ZrTe 5 :Cu 0.05 crystals are synthesized by the chemical vapor transport method in a vacuum. X-ray diffraction and elemental analysis techniques are utilized to validate the synthesis. The results indicate that the intercalation of the layered Zr/Te structure with copper atoms causes the contraction of the unit cell along all three crystalline directions, the shrinkage of the overall volume of the unit cell, and the distortion of the unit cell. A single crystal was isolated, mechanically exfoliated, and used for the measurements of intercalation strains in a Hall bar device. Electronic transport studies indicate that an anomalous resistance drop is observed at T = 19 K. Furthermore, R xx and R xy results, respectively, indicate a probable disorder-induced localization effect and electron-type carriers.

36 MATERIALS SCIENCE↗

Elucidating Actinide–Pertechnetate and Actinide–Perrhenate Bonding via a Family of Th–TcO 4 and Th–ReO 4 Frameworks and Solutions

Technetium-99, a β-emitter produced from 235 U fission, poses a challenge for the nuclear industry due to co-extraction of pertechnetate (TcO 4 – ) with the actinides (An) during nuclear fuel reprocessing. Previous studies suggested that direct coordination of pertechnetate with An plays an important role in the coextraction process. However, few studies have provided direct evidence for An–TcO 4 – bonding in the solid state, and even fewer in solution. The present study describes synthesis and structural elucidation of a family of thorium(IV)-pertechnetate/perrhenate (ReO 4 – , nonradioactive surrogate) compounds, which is obtained by dissolution of thorium oxyhydroxide in perrhenic/pertechnic acid followed by crystallization, with or without heating. For reaction ratios of 3:1, 4:1, and 6:1 MO 4 – /Th(IV) (M = Tc, Re), the crystallized compounds reflect the same ratio, suggesting facile and flexible coordination. Furthermore, nine structures reveal 1-dimensional and 2-dimensional frameworks with varying topologies. While a multitude of compounds isolated from 4:1 (and 6:1) reaction solutions feature Th monomers linked by MO 4 – , the 3:1 reaction solution yielded the well-known dihydroxide-bridged thorium dimer, linked, and capped by MO 4 – . Density functional theory calculations on ReO 4 – /TcO 4 – isomorphs suggest similar bonding characteristics in the solid state, but experimental solution characterization noted differences. Specifically, small-angle X-ray scattering studies suggest the bonding of Th–TcO 4 – persists in solution, while Th–ReO 4 – bonding is less apparent.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗