93 research outputs found

    Dynamics of porous and amorphous magnesium borohydride to understand solid state Mg-ion-conductors

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    Rechargeable solid-state magnesium batteries are considered for high energy density storage and usage in mobile applications as well as to store energy from intermittent energy sources, triggering intense research for suitable electrode and electrolyte materials. Recently, magnesium borohydride, Mg(BH4_{4})2_{2}, was found to be an effective precursor for solid-state Mg-ion conductors. During the mechanochemical synthesis of these Mg-ion conductors, amorphous Mg(BH4_{4})2_{2} is typically formed and it was postulated that this amorphous phase promotes the conductivity. Here, electrochemical impedance spectroscopy of as-received γ-Mg(BH4_{4})2_{2} and ball milled, amorphous Mg(BH4_{4})2_{2} confirmed that the conductivity of the latter is ~2 orders of magnitude higher than in as-received γ-Mg(BH4_{4})2_{2} at 353 K. Pair distribution function (PDF) analysis of the local structure shows striking similarities up to a length scale of 5.1 Å, suggesting similar conduction pathways in both the crystalline and amorphous sample. Up to 12.27 Å the PDF indicates that a 3D net of interpenetrating channels might still be present in the amorphous phase although less ordered compared to the as-received γ-phase. However, quasi elastic neutron scattering experiments (QENS) were used to study the rotational mobility of the [BH4_{4}] units, revealing a much larger fraction of activated [BH4_{4}] rotations in amorphous Mg(BH4_{4})2_{2}. These findings suggest that the conduction process in amorphous Mg(BH4_{4})2_{2} is supported by stronger rotational mobility, which is proposed to be the so-called “paddle-wheel” mechanism

    Energy research with neutrons (ErwiN) and installation of a fast neutron powder diffraction option at the MLZ, Germany

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    The need for rapid data collection and studies of small sample volumes in the range of cubic millimetres are the main driving forces for the concept of a new high-throughput monochromatic diffraction instrument at the Heinz Maier-Leibnitz Zentrum (MLZ), Germany. A large region of reciprocal space will be accessed by a detector with sufficient dynamic range and microsecond time resolution, while allowing for a variety of complementary sample environments. The medium-resolution neutron powder diffraction option for `energy research with neutrons\u27 (ErwiN) at the high-flux FRM II neutron source at the MLZ is foreseen to meet future demand. ErwiN will address studies of energy-related systems and materials with respect to their structure and uniformity by means of bulk and spatially resolved neutron powder diffraction. A set of experimental options will be implemented, enabling time-resolved studies, rapid parametric measurements as a function of external parameters and studies of small samples using an adapted radial collimator. The proposed powder diffraction option ErwiN will bridge the gap in functionality between the high-resolution powder diffractometer SPODI and the time-of-flight diffractometers POWTEX and SAPHiR at the MLZ

    Lithium-ion (de)intercalation mechanism in core-shell layered Li(Ni,Co,Mn)O2 cathode materials

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    LiNix_{x}CoyMn1xy_{1-x-y}O2_{2} (NCM) intercalation compounds with core-shell architecture have been found to be promising cathode candidates for next-generation lithium-ion battery applications. The NCM cathodes\u27 functional properties are dependent on the transition metal relative ratios, making it a challenge to control the real structure of core-shell NCM cathode materials and to understand the synergistic effect of core and shell during the electrochemical cycling. Herein, a universal and facile synthetic strategy is developed to synthesize the NCM material composed of an inner Ni-rich core and a Mn-rich shell on a secondary particle level. Both the Ni-rich particle core and the Mn-rich outer surface possess a layered α–NaFeO2_{2}–type structure with the same space group (R3m). The in situ synchrotron-based X-ray diffraction and absorption spectroscopy results demonstrate that the two layered phases do not participate in the electrochemical reaction simultaneously during the first cycle between 2.7 and 4.3 V, while they exhibit a similar reversible (de)lithiation mechanism in the following cycles. These findings provide a new perspective for rational design of layered Ni-based cathode materials with high energy and long cycling life with particular two phase electrochemical characteristics

    A review of the MSCA ITN ECOSTORE - Novel complex metal hydrides for efficient and compact storage of renewable energy as hydrogen and electricity

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    Hydrogen as an energy carrier is very versatile in energy storage applications. Developments in novel, sustainable technologies towards a CO2-free society are needed and the exploration of all-solid-state batteries (ASSBs) as well as solid-state hydrogen storage applications based on metal hydrides can provide solutions for such technologies. However, there are still many technical challenges for both hydrogen storage material and ASSBs related to designing low-cost materials with low-environmental impact. The current materials considered for all-solid-state batteries should have high conductivities for Na+, Mg2+ and Ca2+, while Al3+-based compounds are often marginalised due to the lack of suitable electrode and electrolyte materials. In hydrogen storage materials, the sluggish kinetic behaviour of solid-state hydride materials is one of the key constraints that limit their practical uses. Therefore, it is necessary to overcome the kinetic issues of hydride materials before discussing and considering them on the system level. This review summarizes the achievements of the Marie Skłodowska-Curie Actions (MSCA) innovative training network (ITN) ECOSTORE, the aim of which was the investigation of different aspects of (complex) metal hydride materials. Advances in battery and hydrogen storage materials for the efficient and compact storage of renewable energy production are discussed

    Metal Hydrides and Related Materials - Energy Carriers for Novel Hydrogen and Electrochemical Storage

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    The seventh edition of the International Renewable and Sustainable Energy Conference (IRSEC) was held in Agadir (Sofitel Royal Bay, November 27–30, Morocco) under the Program Chair of Prof. Ahmed Ennaoui (IRESEN). IRSEC, as one of the biggest conferences in north Africa, aims at creating an international forum to facilitate discussions and exchanges in all aspects of renewable and sustainable energy. This Viewpoint will summarize the scientific presentations and stimulated discussions during the Special Session (November 28–29) on Metal Hydrides’ Energy covering topics of metal hydrides and energy related issues for innovative processes and technologies, with a focus on magnesium-based hydrides, intermetallic hydrides, complex and melt hydrides, porous materials, and thin films

    Identity crisis: A theoretical analysis of ‘team identification’ research.

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    Research question: Existing team identification research uses various definitions, conceptualisations, and theoretical frameworks. In this paper, we provide a theoretical analysis of previous research using the two dominant theoretical approaches: identity theory and the social identity approach. Our primary purpose is to provide a theoretical framework for the on-going study of ‘team’ identification in sport management research. Findings: Scholars have used identity theory (role) and the social identity approach (group) in their quest to understand team identification, however, limited attention has been paid to the differences between the two frameworks. We focus on two aspects of role and group identification that epitomize divergence in terms of analytical focus and explanations for behavior: the basis for identification and salience. Implications. The manuscript concludes with three recommendations for future research. First, with the aim of making future research more specific, we recommend the use of fan (spectator) identification in studies using identity theory and team identification (organisation / brand) in studies exploring the influence of group identity. Second, we outline definitions for role (fan) and group (team) identification in sport research. Finally, we reflect on the measurement of team identification

    Metallic and complex hydride-based electrochemical storage of energy

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    The development of efficient storage systems is one of the keys to the success of the energy transition. There are many ways to store energy, but among them, electrochemical storage is particularly valuable because it can store electrons produced by renewable energies with a very good efficiency. However, the solutions currently available on the market remain unsuitable in terms of storage capacity, recharging kinetics, durability, and cost. Technological breakthroughs are therefore expected to meet the growing need for energy storage. Within the framework of the Hydrogen Technology Collaboration Program—H2TCP Task-40, IEA\u27s expert researchers have developed innovative materials based on hydrides (metallic or complex) offering new solutions in the field of solid electrolytes and anodes for alkaline and ionic batteries. This review presents the state of the art of research in this field, from the most fundamental aspects to the applications in battery prototypes

    Reduced Apaf-1 expression in human cutaneous melanomas

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    Malignant melanoma is a life-threatening skin cancer due to its highly metastatic character and resistance to radio- and chemotherapy. It is believed that the ability to evade apoptosis is the key mechanism for the rapid growth of cancer cells. However, the exact mechanism for failure in the apoptotic pathway in melanoma cells is unclear. p53, the most frequently mutated tumour suppressor gene in human cancers, is a key apoptosis inducer. However, p53 mutation is only found in 15–20% of melanoma biopsies. Recently, it was found that Apaf-1, a downstream target of p53, is inactivated in metastatic melanoma. Specifically, loss of heterozygosity (LOH) of the Apaf-1 gene was found in 40% of metastatic melanoma. To determine if loss of Apaf-1 expression is indeed involved in melanoma progression, we employed the tissue microarray technology and examined Apaf-1 expression in 70 human primary malignant melanoma biopsies by immunohistochemistry. Our data showed that Apaf-1 expression is significantly reduced in melanoma cells compared with normal nevi (χ2=6.02, P=0.014). Our results also revealed that loss of Apaf-1 was not associated with the tumour thickness, ulceration or subtype, patient's gender, age and 5-year survival. In addition, our in vitro apoptosis assay revealed that overexpression of Apaf-1 can sensitise melanoma cells to anticancer drug treatment. Taken together, our data indicate that Apaf-1 expression is significantly reduced in human melanoma and that Apaf-1 may serve as a therapeutic target in melanoma
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