Spectral analysis of Monte Carlo calculated fluence correction and cema conversion factors for high-energy photon beams at different depths

Purpose: The aim of this study is to investigate the depth-dependent detector response of detailed thimble air-filled ionization chambers by calculating spectral charged particle fluence correction factors at different depths in water. Those spectral correction factors will help to understand, how the detector response varies at different depths and what kind of influences disparate effects have on the spectral detector response.Methods: The cema-approach can be used to obtain spectral charged particle fluence-based correction factors for various measurement conditions by substituting the commonly well-known dose conversion factor with a conversion factor based on the dosimetric quantity cema (“converted-energy per unit mass”). The resulting spectral fluence correction factors were calculated with the EGSnrc software toolkit and analyzed for two air-filled cylindrical ionization chambers (PTW type 31021 Semiflex 3D, SNC125c™) at different depths in a water phantom irradiated with a 6 MV linear accelerator x-ray spectrum. The ionization chamber models have been stepwise decomposed to investigate the perturbation caused by internal and external effects on the fluence distribution within the detector.Results: Monte Carlo calculated fluence-based perturbation correction factors revealed that for all investigated detectors, considerable fluence disturbances occur, especially in the build-up region of depth-dose curves. Our results have shown that even slight variations in depth can have major consequences on the differential charged particle fluence within the ionization chamber, mainly due to internal cavity-specific effects. Furthermore, the results showed that in the case of relative dose measurements, the depth-depending detector response can significantly differ from unity in a range of 1.4%–2.8% depending on the ionization chamber design.Conclusion: The complexity of different effects on the fluence disturbance could be broken down with regard to their influence on the spectral fluence distribution in the sensitive volume of the investigated detectors. It could be demonstrated, that the displacement of water is a depth-depending effect, which can not be compensated or corrected ideally for each investigated water depth by the shift of the effective point of measurement. Generally, the spectral analysis of those energy-dependent correction factors serves to a deeper understanding of the detector response under various conditions

Drying of NCM Cathode Electrodes with Porous, Nanostructured Particles Versus Compact Solid Particles: Comparative Study of Binder Migration as a Function of Drying Conditions

Porous, nanostructured Li(NiₓCo$_{y}$Mn)O₂ (NCM) achieves an improvement in the fast-charging capability and the durability of lithium-ion batteries. This improvement is attributed to an extended electrolyte—active material interface, where the electrochemical reactions take place and thus shorter diffusion paths inside the active material particles are necessary for charge transfer. Due to the porous particle morphology, new processing challenges arise compared to compact solid NCM. Herein, the properties of the slurries and the electrodes made of the two active materials and, in particular, the influence of the drying process on the binder distribution, are comparatively investigated. For the same composition of the slurries, a significantly lower dependence of adhesion force and discharge capacity at higher C-rates on the drying rate is shown when using porous, nanostructured particles instead of solid particles. Binder migration and thus an inhomogeneous concentration distribution of the polyvinylidene fluoride binder is less pronounced for these electrodes during faster drying. Cell tests with half cells show that after increasing the drying rate by more than 350%, the discharge capacity of the electrodes consisting of solid NCM is reduced by about 63% at 5C while for the electrodes made of porous material no reduction is measured

Process and Drying Behavior Toward Higher Drying Rates of Hard Carbon Anodes for Sodium‐Ion Batteries with Different Particle Sizes: An Experimental Study in Comparison to Graphite for Lithium‐Ion‐Batteries

Sodium-ion batteries are considered to be one of the most promising postlithium batteries on the verge of commercialization. The electrode processing is expected to be similar to lithium-ion batteries. However, the producibility and material processing challenges of potential electrode materials for anodes and cathodes are poorly understood. For industrial electrode production, a deep understanding of the processing of electrode materials with different particle morphologies is of great importance. In particular, the correlation between the process conditions and the electrode properties needs to be investigated further to understand the complex interactions between the battery slurry materials, the binder system, the drying process, and the microstructure formation. One promising anode material is hard carbon. The water-based processing of hard carbon slurries presented in this article shows that the drying behavior is strongly interconnected with the particle size and particle interactions in the drying electrode. This study shows that all the hard carbons investigated do not exhibit binder migration at moderate drying rates. Even at very high drying rates (9 g m−2 s−1, 12 s drying time), an increase in adhesion force of up to 39% is observed for comparatively smaller particles compared to the adhesion force at lower drying rate

Enabling Long‐term Cycling Stability of Na₃V₂(PO₄)₃ /C vs . Hard Carbon Full‐cells

Sodium-ion batteries are becoming an increasingly important complement to lithium-ion batteries. However, while extensive knowledge on the preparation of Li-ion batteries with excellent cycling behavior exists, studies on applicable long-lasting sodium-ion batteries are still limited. Therefore, this study focuses on the cycling stability of batteries composed of Na3V2(PO4)3/C based cathodes and hard carbon anodes. It is shown that full-cells with a decent stability are obtained for ethylene carbonate/propylene carbonate electrolyte and the conducting salt NaPF6. With cathode loadings of 1.2 mAh/cm2, after cell formation discharge capacities up to 92.6 mAh/g are obtained, and capacity retentions >90 % over 1000 charge/discharge cycles at 0.5 C/0.5 C are observed. It is shown that both, the additive fluoroethylene carbonate and impurities in the electrolyte, negatively affect the overall discharge capacity and cycling stability and should therefore be avoided. Remarkably, the internal resistances of well-balanced and well-built cells did not increase over 1500 cycles and 5 months of testing, which is a very promising result regarding the possible lifespan of the cells. The initial loss of active sodium ions in hard carbon remains a major problem, which can only be partially reduced by proper balancing

Drying of Compact and Porous NCM Cathode Electrodes in Different Multilayer Architectures: Influence of Layer Configuration and Drying Rate on Electrode Properties

Porous, nanostructured particles ensure the wetting of electrolyte up to the particle core and shortened diffusion paths, which is relevant not only for lithium-ion batteries but also for postlithium systems like sodium-ion batteries. The porous structure leads to a high C-rate capability. However, compared to conventional compact NCM, porous NCM shows a reduced adhesion force but no or only slight negative influence on C-rate capability by binder migration at higher drying rates. Herein, a multilayer concept is used to increase the adhesion force with equal or better electrochemical performance compared to single-layer electrodes. Compact particles of high volumetric energy density and porous particles with high C-rate capability are combined in a simultaneously coated multilayer electrode. Multilayers with compact NCM toward the current collector and porous NCM with reduced binder content toward the separator side show an about 16-times higher adhesion force at lower drying rate and an about ten-times higher adhesion force at increased drying rate compared to electrodes produced of porous NCM only. The specific discharge capacity of the multilayers is increased by 88% at the lower and 67% at the higher drying rate for a discharge rate of 3C compared to a single layer with compact NCM

Methodology for the characterization and understanding of longitudinal wrinkling during calendering of lithium-ion and sodium-ion battery electrodes

"The manufacturing of lithium-ion battery (LIB) cells is following a complex process chain in which the individual process steps influence the subsequent ones. Meanwhile, increasing requirements especially concerning the battery performance, sustainability and costs are forcing the development of innovative battery materials, production technologies and battery designs. The calendering process directly affects the volumetric energy density of an electrode and therefore of a battery cell. Calendering is still challenging as it causes high stresses in the electrode that lead to defects and thus increased rejection rates. The interaction between electrode material and process as well as the formation of defects is still not fully understood, especially when new material systems are used. In this context, the sodium-ion battery (SIB) is one post-lithium battery system that is a promising option to overcome the limitations of conventional LIBs. Therefore, this paper presents a first material and machine independent methodology to describe and understand the defect type longitudinal wrinkle, which mostly appears at the uncoated current collector edge of an electrode and in running direction. The aim is to systematically characterize the longitudinal wrinkles according to their geometry. The automatic data acquisition is carried out with a laser triangulation system and a 3D scanning system. The geometry values are calculated from the raw data and correlated to selected process parameters. The methodology is applicable regardless of the material as shown by exemplary results of NMC811 cathodes for LIB and hard carbon anodes for SIB. By using two different pilot calenders it is shown, that the data acquisition can be carried out independently of the machine. The presented methodology contributes to finding solutions for the avoidance of longitudinal wrinkling in any battery electrode and therefore to reducing the rejection rate.

Expanded Hemodialysis ameliorates uremia-induced impairment of vasculoprotective KLF2 and concomitant proinflammatory priming of endothelial cells through an ERK/AP1/cFOS-dependent mechanism

AimsExpanded hemodialysis (HDx) therapy with improved molecular cut-off dialyzers exerts beneficial effects on lowering uremia-associated chronic systemic microinflammation, a driver of endothelial dysfunction and cardiovascular disease (CVD) in hemodialysis (HD) patients with end-stage renal disease (ESRD). However, studies on the underlying molecular mechanisms are still at an early stage. Here, we identify the (endothelial) transcription factor Krüppel-like factor 2 (KLF2) and its associated molecular signalling pathways as key targets and regulators of uremia-induced endothelial micro-inflammation in the HD/ESRD setting, which is crucial for vascular homeostasis and controlling detrimental vascular inflammation.Methods and resultsFirst, we found that human microvascular endothelial cells (HMECs) and other typical endothelial and kidney model cell lines (e.g. HUVECs, HREC, and HEK) exposed to uremic serum from patients treated with two different hemodialysis regimens in the Permeability Enhancement to Reduce Chronic Inflammation II (PERCI-II) crossover clinical trial - comparing High-Flux (HF) and Medium Cut-Off (MCO) membranes - exhibited strongly reduced expression of vasculoprotective KLF2 with HF dialyzers, while dialysis with MCO dialyzers led to the maintenance and restoration of physiological KLF2 levels in HMECs. Mechanistic follow-up revealed that the strong downmodulation of KLF2 in HMECs exposed to uremic serum was mediated by a dominant engagement of detrimental ERK instead of beneficial AKT signalling, with subsequent AP1-/c-FOS binding in the KLF2 promoter region, followed by the detrimental triggering of pleiotropic inflammatory mediators, while the introduction of a KLF2 overexpression plasmid could restore physiological KLF2 levels and downmodulate the detrimental vascular inflammation in a mechanistic rescue approach.ConclusionUremia downmodulates vasculoprotective KLF2 in endothelium, leading to detrimental vascular inflammation, while MCO dialysis with the novel improved HDx therapy approach can maintain physiological levels of vasculoprotective KLF2