477 results match your criteria: "Institute Ulm.[Affiliation]"

Low-Temperature Lithium Metal Batteries Achieved by Synergistically Enhanced Screening Li Desolvation Kinetics.

Adv Mater

December 2024

State Key Laboratory of Featured Metal Materials and Life-cycle Safety for Composite Structures, Guangxi Key Laboratory of Processing for Non-Ferrous Metals and Featured Materials, School of Resources, Environment and Materials, Guangxi University, Nanning, 530004, China.

Lithium metal anode is desired by high capacity and low potential toward higher energy density than commercial graphite anode. However, the low-temperature Li metal batteries suffer from dendrite formation and dead Li resulting from uneven Li behaviors of flux with huge desolvation/diffusion barriers, thus leading to short lifespan and safety concern. Herein, differing from electrolyte engineering, a strategy of delocalizing electrons with generating rich active sites to regulate Li desolvation/diffusion behaviors are demonstrated via decorating polar chemical groups on porous metal-organic frameworks (MOFs).

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Next-generation battery technologies need to consider their environmental impact throughout the whole cycle life, which has brought new chemistries based on earth-abundant elements to the spotlight. Rechargeable calcium batteries are such an emerging technology, which shows the potential to provide high cell voltage and high energy density close to lithium-ion batteries. Additionally, the use of Ca2+ as a charge carrier renders significant sustainable values.

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The class-wide restriction proposal on perfluoroalkyl and polyfluoroalkyl substances (PFAS) in the European Union is expected to affect a wide range of commercial sectors, including the lithium-ion battery (LIB) industry, where both polymeric and low molecular weight PFAS are used. The PFAS restriction dossiers currently state that there is weak evidence for viable alternatives to the use of PFAS in LIBs. In this Perspective, we summarize both the peer-reviewed literature and expert opinions from academia and industry to verify the legitimacy of the claims surrounding the lack of alternatives.

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Lithium-ion batteries, due to their high energy density, compact size, long lifetime, and low environmental impact, have achieved a dominant position in everyday life. These attributes have made them the preferred choice for powering portable devices such as laptops and smartphones, power tools, and electric vehicles. As technology advances rapidly, the demand for even more efficient energy storage devices continues to rise.

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Slow Voltage Relaxation of Silicon Nanoparticles with a Chemo-Mechanical Core-Shell Model.

ACS Appl Mater Interfaces

December 2024

Institute of Engineering Thermodynamics, German Aerospace Center (DLR), Wilhelm-Runge-Straße 10, Ulm 89081, Germany.

Silicon presents itself as a high-capacity anode material for lithium-ion batteries with a promising future. The high ability for lithiation comes along with massive volume changes and a problematic voltage hysteresis, causing reduced efficiency, detrimental heat generation, and a complicated state-of-charge estimation. During slow cycling, amorphous silicon nanoparticles show a larger voltage hysteresis than after relaxation periods.

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Non-volatile memristors dynamically switch between high (HRS) and low resistance states (LRS) in response to electrical stimuli, essential for electronic memories, neuromorphic computing, and artificial intelligence. High-entropy Prussian blue analogs (HE-PBAs) are promising insertion-type battery materials due to their diverse composition, high structural integrity, and favorable ionic conductivity. This work proposes a non-volatile, bipolar memristor based on HE-PBA.

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The high-voltage oxygen redox activity of Li-rich layered oxides enables additional capacity beyond conventional transition metal (TM) redox contributions and drives the development of positive electrode active materials in secondary Li-based batteries. However, Li-rich layered oxides often face voltage decay during battery operation. In particular, although Li-rich positive electrode active materials with a high nickel content demonstrate improved voltage stability, they suffer from poor discharge capacity.

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Rechargeable magnesium batteries are promising for future energy storage. However, among other challenges, their practical application is hindered by low coulombic efficiencies of magnesium plating and stripping. Fundamental processes such as the formation, structure, and stability of passivation layers and the influence of different electrolyte components on them are still not fully understood.

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Article Synopsis
  • Low-temperature lithium-sulfur batteries (LT-LSB) face challenges with the slow movement of lithium ions and polysulfide conversion.
  • A new approach involves using oxygen-defective vanadium trioxide supported on a porous carbon network to improve electron delocalization and hybridization, enhancing interactions with sulfur species.
  • At low temperatures, the modified battery shows impressive performance, achieving 501 mA h/g at 0°C and retaining 85% capacity after 100 cycles at -10°C, significantly improving operational longevity and efficiency.
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Article Synopsis
  • * NMR spectroscopy and simulations show that smaller graphene-like domains in these carbons are linked to higher capacitance levels.
  • * Raman spectroscopy supports these findings, indicating that broader D bands and lower I/I intensity ratios relate to increased capacitance, proving it to be an effective tool for identifying high-performance nanoporous carbons for supercapacitors.
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  • Hydrogen titanates (HTOs) are layered titanium oxides with an interlayer that holds water and protons, influencing lithium insertion during electrochemical processes.
  • The study employed various techniques like X-ray diffraction and mass spectroscopy to analyze how the interlayer chemistry affects the electrochemical responses of different HTOs (HTiO·HO with n = 3, 4, and 5).
  • Findings suggest that the first reduction reaction relates to the acidity of structural protons, leading to hydrogen gas production and the formation of a lithiated hydrogen titanate, impacting our understanding of electrochemical behaviors in materials with hydrogen and water.
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Screening Ammonium-Based Cationic Additives to Regulate Interfacial Chemistry for Aqueous Ultra-Stable Zn Metal Anode.

Adv Sci (Weinh)

November 2024

Key Laboratory of Engineering Dielectric and Applications (Ministry of Education), School of Electrical and Electronic Engineering, Harbin University of Science and Technology, Harbin, 150080, P. R. China.

Article Synopsis
  • The dynamics and chemistry at the electrolyte/metal interface are crucial for the reversible deposition and dissolution of zinc in battery systems.
  • Different cationic ammonium-based additives can enhance this interfacial chemistry, leading to better performance in zinc anodes.
  • Specifically, tetramethylammonium shows a unique ability to stabilize the solvation shell around zinc, resulting in significantly improved efficiency and long-lasting performance in both symmetric and asymmetric battery configurations.
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Scalable Li-Ion Battery with Metal/Metal Oxide Sulfur Cathode and Lithiated Silicon Oxide/Carbon Anode.

ChemSusChem

September 2024

Department of Chemical, Pharmaceutical and Agricultural Sciences, University of Ferrara, via Fossato di Mortara 17, 44121, Ferrara, Italy.

A Li-ion battery combines a cathode benefitting from Sn and MnO with high sulfur content, and a lithiated anode including fumed silica, few layer graphene (FLG) and amorphous carbon. This battery is considered a scalable version of the system based on lithium-sulfur (Li-S) conversion, since it exploits at the anode the Li-ion electrochemistry instead of Li-metal stripping/deposition. Sn and MnO are used as cathode additives to improve the electrochemical process, increase sulfur utilization, while mitigating the polysulfides loss typical of Li-S devices.

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The energy density of lithium-metal batteries (LMBs) relies substantially on the thickness of the lithium-metal anode. However, a bare, thin lithium foil electrode is vulnerable to fragmentation due to the inhomogeneity of the lithium stripping/plating process, disrupting the electron conduction pathway along the electrode. Accordingly, the current collector is an integral part to prevent the resulting loss of electronic conductivity.

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Sustainable batteries are key for powering electronic devices of the future, with aqueous zinc-ion batteries (AZIBs) standing out for their use of abundant, readily available elements, and safer production processes. Among the various electrode materials studied for AZIBs, the Chevrel Phase, MoS has shown promise due to its open framework, but issues with zinc ion trapping have limited its practical application. In this work, we employed computational methods to investigate the insertion-deinsertion mechanism in a series of isostructural MoSSe ( = 0-8) solid solutions as materials that could balance the gravimetric capacity and reversible cycling for AZIBs.

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Self-Healable, High-Stability Anode for Rechargeable Magnesium Batteries Realized by Graphene-Confined Gallium Metal.

Nano Lett

September 2024

National Engineering Research Center for Magnesium Alloys, College of Materials Science and Engineering, Chongqing University, 400044 Chongqing, China.

Article Synopsis
  • A novel anode material for rechargeable magnesium batteries (RMBs) was created, featuring a core-shell structure of gallium (Ga) encapsulated by reduced graphene oxide (rGO).
  • The Ga@rGO anode exhibits impressive performance, achieving a specific capacity of 150 mAh/g at 0.5 A/g for 1200 cycles at room temperature and 100 mAh/g at 1 A/g for 700 cycles at 40 °C.
  • Utilizing a cost-effective and eco-friendly direct drop coating method, the anode demonstrates not only high cycling stability and rate performance but also a self-healing ability even under extreme charging conditions, making it a promising candidate for advanced RMB technologies.
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Article Synopsis
  • Researchers applied advanced engineering techniques to improve Prussian blue analogue (PBA) cathodes, exploring both cubic and monoclinic crystal structures.
  • They used various characterization methods to study the electrochemical behavior of these PBAs, revealing key insights into their performance.
  • The cubic PBA structure showed notable advantages after optimization, including better cycling stability, good reversibility, minimal capacity loss, and high thermal stability even under challenging conditions.
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Rechargeable magnesium batteries (RMBs) have the potential to provide a sustainable and long-term solution for large-scale energy storage due to high theoretical capacity of magnesium (Mg) metal as an anode, its competitive redox potential (Mg/Mg:-2.37 V vs. SHE) and high natural abundance.

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Defect engineering is a key chemical tool to modulate the electronic structure and reactivity of nanostructured catalysts. Here, it is reported how targeted introduction of defect sites in a 2D palladium metallene nanostructure results in a highly active catalyst for the alkaline oxygen reduction reaction (ORR). A defect-rich WO and MoO modified Pd metallene (denoted: D-Pd M) is synthesized by a facile and scalable approach.

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Gel Polymer Electrolyte Enables Low-Temperature and High-Rate Lithium-Ion Batteries via Bionic Interface Design.

Small

November 2024

Key Laboratory of Automobile Materials of MOE, School of Materials Science and Engineering, and Jilin Provincial International Cooperation Key Laboratory of High-Efficiency Clean Energy Materials, Jilin University, Changchun, 130013, P. R. China.

Traditional ethylene carbonate (EC)-based electrolytes constrain the applications of silicon carbon (Si-C) anodes under fast-charging and low-temperature conditions due to sluggish Li migration kinetics and unstable solid electrolyte interphase (SEI). Herein, inspired by the efficient water purification and soil stabilization of aquatic plants, a stable SEI with a 3D desolvation interface is designed with gel polymer electrolyte (GPE), accelerating Li desolvation and migration at the interface and within stable SEI. As demonstrated by theoretical simulations and experiment results, the resulting poly(1,3-dioxolane) (PDOL), prepared by in situ ring-opening polymerization of 1,3-dioxolane (DOL), creates a 3D desolvation area, improving the Li desolvation at the interface and yielding an amorphous GPE with a high Li ionic conductivity (5.

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High-entropy nanomaterials exhibit exceptional mechanical, physical, and chemical properties, finding applications in many industries. Peroxidases are metalloenzymes that accelerate the decomposition of hydrogen peroxide. This study uses the high-entropy approach to generate multimetal oxide-based nanozymes with peroxidase-like activity and explores their application as sensors in bioassays.

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The nanoscale form of the Chevrel phase, MoS, is demonstrated to be a highly efficient zinc-free anode in aqueous zinc ion hybrid supercapacitors (ZIHSCs). The unique morphological characteristics of the material when its dimensions approach the nanoscale result in fast zinc intercalation kinetics that surpass the ion transport rate reported for some of the most promising materials, such as TiS and TiSe. Raman spectroscopy, post-mortem X-ray diffraction, Hard X-ray photoelectron spectroscopy, and density functional theory (DFT) calculations were combined to understand the overall mechanism of the zinc ion (de)intercalation process.

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K-Doping Suppresses Oxygen Redox in P2-NaNiCuMnO Cathode Materials for Sodium-Ion Batteries.

Small

October 2024

Bavarian Center for Battery Technology (BayBatt), Universität Bayreuth, Weiherstr. 26, 95448, Bayreuth, Germany.

In P2-type layered oxide cathodes, Na site-regulation strategies are proposed to modulate the Na distribution and structural stability. However, their impact on the oxygen redox reactions remains poorly understood. Herein, the incorporation of K in the Na layer of NaNiCuMnO is successfully applied.

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Engineering of Aromatic Naphthalene and Solvent Molecules to Optimize Chemical Prelithiation for Lithium-Ion Batteries.

Adv Sci (Weinh)

August 2024

Department of Materials Science and Engineering, National Yang Ming Chiao Tung University, 1001 University Road, Hsinchu, 30010, Taiwan.

A cost-effective chemical prelithiation solution, which consists of Li, polyaromatic hydrocarbon (PAH), and solvent, is developed for a model hard carbon (HC) electrode. Naphthalene and methyl-substituted naphthalene PAHs, namely 2-methylnaphthalene and 1-methylnaphthalene, are first compared. Grafting an electron-donating methyl group onto the benzene ring can decrease electron affinity and thus reduce the redox potential, which is validated by density functional theory calculations.

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Covalent organic frameworks (COFs) containing well-defined redox-active groups have become competitive materials for next-generation batteries. Although high potentials and rate performance can be expected, only a few examples of p-type COFs have been reported for charge storage to date with even fewer examples on the use of COFs in multivalent ion batteries. Herein, we report the synthesis of a p-type highly porous and crystalline azatruxene-based COF and its application as a positive electrode material in Li- and Mg-based batteries.

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