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    High‐Entropy Sulfides as Electrode Materials for Li‐Ion Batteries
    (Weinheim : Wiley-VCH, 2022) Lin, Ling; Wang, Kai; Sarkar, Abhishek; Njel, Christian; Karkera, Guruprakash; Wang, Qingsong; Azmi, Raheleh; Fichtner, Maximilian; Hahn, Horst; Schweidler, Simon; Breitung, Ben
    High-entropy sulfides (HESs) containing 5 equiatomic transition metals (M), with different M:S ratios, are prepared by a facile one-step mechanochemical approach. Two new types of single-phase HESs with pyrite (Pa-3) and orthorhombic (Pnma) structures are obtained and demonstrate a homogeneously mixed solid solution. The straightforward synthesis method can easily tune the desired metal to sulfur ratio for HESs with different stoichiometries, by utilizing the respective metal sulfides, even pure metals, and sulfur as precursor chemicals. The structural details and solid solution nature of HESs are studied by X-ray diffraction, transmission electron microscopy, energy-dispersive X-ray spectroscopy, electron energy loss spectroscopy, X-ray photoelectron spectroscopy, inductively coupled plasma optical emission spectroscopy, and Mössbauer spectroscopy. Since transition metal sulfides are a very versatile material class, here the application of HESs is presented as electrode materials for reversible electrochemical energy storage, in which the HESs show high specific capacities and excellent rate capabilities in secondary Li-ion batteries.
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    Transparent Power-Generating Windows Based on Solar-Thermal-Electric Conversion
    (Weinheim : Wiley-VCH, 2021) Zhang, Qihao; Huang, Aibin; Ai, Xin; Liao, Jincheng; Song, Qingfeng; Reith, Heiko; Cao, Xun; Fang, Yueping; Schierning, Gabi; Nielsch, Kornelius; Bai, Shengqiang; Chen, Lidong
    Integrating transparent solar-harvesting systems into windows can provide renewable on-site energy supply without altering building aesthetics or imposing further design constraints. Transparent photovoltaics have shown great potential, but the increased transparency comes at the expense of reduced power-conversion efficiency. Here, a new technology that overcomes this limitation by combining solar-thermal-electric conversion with a material's wavelength-selective absorption is presented. A wavelength-selective film consisting of Cs0.33WO3 and resin facilitates high visible-light transmittance (up to 88%) and outstanding ultraviolet and infrared absorbance, thereby converting absorbed light into heat without sacrificing transparency. A prototype that couples the film with thermoelectric power generation produces an extraordinary output voltage of ≈4 V within an area of 0.01 m2 exposed to sunshine. Further optimization design and experimental verification demonstrate high conversion efficiency comparable to state-of-the-art transparent photovoltaics, enriching the library of on-site energy-saving and transparent power generation.
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    Current State-of-the-Art in the Interface/Surface Modification of Thermoelectric Materials
    (Weinheim : Wiley-VCH, 2021) He, Shiyang; Lehmann, Sebastian; Bahrami, Amin; Nielsch, Kornelius
    Thermoelectric (TE) materials are prominent candidates for energy converting applications due to their excellent performance and reliability. Extensive efforts for improving their efficiency in single-/multi-phase composites comprising nano/micro-scale second phases are being made. The artificial decoration of second phases into the thermoelectric matrix in multi-phase composites, which is distinguished from the second-phase precipitation occurring during the thermally equilibrated synthesis of TE materials, can effectively enhance their performance. Theoretically, the interfacial manipulation of phase boundaries can be extended to a wide range of materials. High interface densities decrease thermal conductivity when nano/micro-scale grain boundaries are obtained and certain electronic structure modifications may increase the power factor of TE materials. Based on the distribution of second phases on the interface boundaries, the strategies can be divided into discontinuous and continuous interfacial modifications. The discontinuous interfacial modifications section in this review discusses five parts chosen according to their dispersion forms, including metals, oxides, semiconductors, carbonic compounds, and MXenes. Alternatively, gas- and solution-phase process techniques are adopted for realizing continuous surface changes, like the core–shell structure. This review offers a detailed analysis of the current state-of-the-art in the field, while identifying possibilities and obstacles for improving the performance of TE materials.
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    Applications of Carbon Nanotubes in the Internet of Things Era
    (Berlin ; Heidelberg [u.a.] : Springer, 2021) Pang, Jinbo; Bachmatiuk, Alicja; Yang, Feng; Liu, Hong; Zhou, Weijia; Rümmeli, Mark H.; Cuniberti, Gianaurelio
    The post-Moore's era has boosted the progress in carbon nanotube-based transistors. Indeed, the 5G communication and cloud computing stimulate the research in applications of carbon nanotubes in electronic devices. In this perspective, we deliver the readers with the latest trends in carbon nanotube research, including high-frequency transistors, biomedical sensors and actuators, brain-machine interfaces, and flexible logic devices and energy storages. Future opportunities are given for calling on scientists and engineers into the emerging topics.
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    Influence of nanobody binding on fluorescence emission, mobility, and organization of GFP-tagged proteins
    (Amsterdam [u.a.] : Elsevier, 2020) Schneider, Falk; Sych, Taras; Eggeling, Christian; Sezgin, Erdinc
    Advanced fluorescence microscopy studies require specific and monovalent molecular labeling with bright and photostable fluorophores. This necessity led to the widespread use of fluorescently labeled nanobodies against commonly employed fluorescent proteins (FPs). However, very little is known how these nanobodies influence their target molecules. Here, we tested commercially available nanobodies and observed clear changes of the fluorescence properties, mobility and organization of green fluorescent protein (GFP) tagged proteins after labeling with the anti-GFP nanobody. Intriguingly, we did not observe any co-diffusion of fluorescently labeled nanobodies with the GFP-labeled proteins. Our results suggest significant binding of the nanobodies to a non-emissive, likely oligomerized, form of the FPs, promoting disassembly into monomeric form after binding. Our findings have significant implications on the application of nanobodies and GFP labeling for studying dynamic and quantitative protein organization in the plasma membrane of living cells using advanced imaging techniques.
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    ZnO Nanoparticles Encapsulated in Nitrogen-Doped Carbon Material and Silicalite-1 Composites for Efficient Propane Dehydrogenation
    (Amsterdam [u.a.] : Elsevier, 2019) Zhao, Dan; Li, Yuming; Han, Shanlei; Zhang, Yaoyuan; Jiang, Guiyuan; Wang, Yajun; Guo, Ke; Zhao, Zhen; Xu, Chunming; Li, Ranjia; Yu, Changchun; Zhang, Jian; Ge, Binghui; Kondratenko, Evgenii V.
    Chemistry; Catalysis; Nanoparticles © 2019 The Author(s)Non-oxidative propane dehydrogenation (PDH)is an attractive reaction from both an industrial and a scientific viewpoint because it allows direct large-scale production of propene and fundamental analysis of C-H activation respectively. The main challenges are related to achieving high activity, selectivity, and on-stream stability of environment-friendly and cost-efficient catalysts without non-noble metals. Here, we describe an approach for the preparation of supported ultrasmall ZnO nanoparticles (2–4 nm, ZnO NPs)for high-temperature applications. The approach consists of encapsulation of NPs into a nitrogen-doped carbon (NC)layer in situ grown from zeolitic imidazolate framework-8 on a Silicalite-1 support. The NC layer was established to control the size of ZnO NPs and to hinder their loss to a large extent at high temperatures. The designed catalysts exhibited high activity, selectivity, and on-stream stability in PDH. Propene selectivity of about 90% at 44.4% propane conversion was achieved at 600°C after nearly 6 h on stream. © 2019 The Author(s)
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    The Exploration of Aroyltrimethylgermane as Potent Synthetic Origins and Their Preparation
    (Amsterdam [u.a.] : Elsevier, 2019) Yuan, Yang; Zhang, Youcan; Chen, Bo; Wu, Xiao-Feng
    The synthetic utilities of acylgermanes are surprisingly rarely explored compared with their analogues. In this communication, the survey of aroyltrimethylgermane as potent synthetic origins has been studied. A variety of novel chemical transformations have been realized, including using the acylgermane group as a directing group in Rh-catalyzed aromatic C-H alkenylation reaction and Ir-catalyzed aromatic C-H amidation reactions. Additionally, a general approach for acylgermanes preparation has been established as well. The catalytic system proceeds effectively in the presence of Pd(OAc)2/BINOL-based monophosphite (L11) and allows for the straightforward access to a wide range of functionalized acylgermanes in high yields. © 2019 The Author(s)Catalysis; Organic Synthesis; Organic Reaction; Chemical Synthesis © 2019 The Author(s)
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    Regulation of Two-Dimensional Lattice Deformation Recovery
    (Amsterdam [u.a.] : Elsevier, 2019) Liu, Jinxin; Zhou, Lu; Huang, Ke; Song, Xianyin; Chen, Yunxu; Liang, Xiaoyang; Gao, Jin; Xiao, Xiangheng; Rümmeli, Mark H.; Fu, Lei
    The lattice directly determines the electronic structure, and it enables controllably tailoring the properties by deforming the lattices of two-dimensional (2D)materials. Owing to the unbalanced electrostatic equilibrium among the dislocated atoms, the deformed lattice is thermodynamically unstable and would recover to the initial state. Here, we demonstrate that the recovery of deformed 2D lattices could be directly regulated via doping metal donors to reconstruct electrostatic equilibrium. Compared with the methods that employed external force fields with intrinsic instability and nonuniformity, the stretched 2D molybdenum diselenide (MoSe2)could be uniformly retained and permanently preserved via doping metal atoms with more outermost electrons and smaller electronegativity than Mo. We believe that the proposed strategy could open up a new avenue in directly regulating the atomic-thickness lattice and promote its practical applications based on 2D crystals. © 2019 The Author(s)
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    On-Chip Micro Temperature Controllers Based on Freestanding Thermoelectric Nano Films for Low-Power Electronics
    (Berlin ; Heidelberg [u.a.] : Springer, 2024) Jin, Qun; Guo, Tianxiao; Pérez, Nicolás; Yang, Nianjun; Jiang, Xin; Nielsch, Kornelius; Reith, Heiko
    Dense and flat freestanding Bi2Te3-based thermoelectric nano films were successfully fabricated by sputtering technology using a newly developed nano graphene oxide membrane as a substrate. On-chip micro temperature controllers were integrated using conventional micro-electromechanical system technology, to achieve energy-efficient temperature control for low-power electronics. The tunable equivalent thermal resistance enables an ultrahigh temperature control capability of 100 K mW−1 and an ultra-fast cooling rate exceeding 2000 K s−1, as well as excellent reliability of up to 1 million cycles.
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    The point charge oscillator: Qualitative and analytical investigations
    (Vilnius : Vilnius Gediminas Technical University, 2019) Schneider, Klaus R.
    We study the mathematical model of the point charge oscillator which has been derived by A. Belendez et al. [2]. First we determine the global phase portrait of this model in the Poincare disk. It consists of a family of closed orbits surrounding the unique finite equilibrium point and of a continuum of homoclinic orbits to the unique equilibrium point at infinity. Next we derive analytic expressions for the relationship between period (frequency) and amplitude. Further, we prove that the period increases monotone with the amplitude and derive an expression for its growth rate as the amplitude tends to infinity. Finally, we determine a relation between period and amplitude by means of the complete elliptic integral of the first kind K(k) and of the Jacobi elliptic function cn.