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Correlation versus dissipation in a non-Hermitian Anderson impurity model

Physical Review B 2025年第12期111卷 125157-125157页

作者： Kazuki Yamamoto Masaya Nakagawa Norio Kawakami Department of Physics Tokyo Institute of Technology Meguro Tokyo 152-8551 Japan Department of Physics University of Tokyo Hongo Tokyo 113-0033 Japan Fundamental Quantum Science Program TRIP Headquarters RIKEN Wako 351-0198 Japan Department of Physics Ritsumeikan University Kusatsu Shiga 525-8577 Japan Department of Materials Engineering Science Osaka University Toyonaka Osaka 560-8531 Japan

We analyze the competition between strong correlations and dissipation in quantum impurity systems from the Kondo regime to the valence fluctuation regime by developing a slave-boson theory for a non-Hermitian Anderson impurity model with one-body loss. Notably, in the non-Hermitian Kondo regime, strong correlations qualitatively change the nature of dissipation through renormalization effects, where the effective one-body loss is suppressed and emergent many-body dissipation characterized by the complex-valued hybridization is generated. We unveil the mechanism of a dissipative quantum phase transition of the Kondo state on the basis of this renormalization effect, which counterintuitively enhances the lifetime of the impurity against loss. We also find a crossover from the non-Hermitian Kondo regime to the valence fluctuation regime dominated by one-body dissipation. Our results can be tested in a wide variety of setups such as quantum dots coupled to electronic leads and quantum point contacts in ultracold Fermi gases.

关键词： Bosons

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Gradient Design with Low-Tortuosity Overcoming Kinetic Limitations in High-Loading Solid-State Cathodes

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Angewandte Chemie 2025年

作者： Guangzeng Cheng Jinping Yu Yonghui Wang Zhengyu Ju Yue Zhu Weiqian Tian Jingwei Chen Huanlei Wang Jingyi Wu Guihua Yu School of Materials Science and Engineering Ocean University of China Qingdao 266404 China Materials Science and Engineering Program and Walker Department of Mechanical Engineering The University of Texas at Austin Austin Texas 78712 USA

The extensive commercialization of practical solid-state batteries (SSBs) necessitates the development of high-loading solid-state cathodes with fast charging capability. However, electrochemical kinetics are severely delayed in thick cathodes due to tortuous ion transport pathways and slow solid-solid ion diffusion, which limit the achievable capacity of SSBs at high current densities. In this work, we propose a conductivity gradient cathode with low-tortuosity to enable facile ion transport and counterbalance ion concentration gradient, thereby overcoming the kinetic limitations and achieving fast charging capabilities in thick cathodes. The LiNi 0.8 Co 0.1 Mn 0.1 O 2 cathodes deliver a room-temperature (RT) capacities of 147 and 110 mAh g −1 at 5 C and 10 C, respectively, and meanwhile achieve a RT areal capacity of 3.3 mAh cm −2 at 3 C, enabling SSBs simultaneously high energy and power densities. The universality of this strategy is demonstrated in LiFePO 4 cathodes, providing a novel solution for fast charging and large-scale application of high-loading SSBs.

关键词： solid-state battery composite cathode high-loading gradient low-tortuosity

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EFFECT OF REINFORCEMENT SIZE ON AGE-HARDENING OF PM-2009 AL-SIC 20 VOL-PERCENT PARTICULATE COMPOSITES

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JOURNAL OF materials science 1995年第17期30卷 4316-4322页

作者： SANNINO, AP RACK, HJ Materials Science and Engineering Program Department of Mechanical Engineering Clemson University Clemson USA

The influence of SiC particulate size on the age-hardening response of 2009 aluminium has been monitored utilizing hardness, electrical conductivity and differential scanning calorimetry. Ageing involved either two or three stages depending on the reinforcement size. For 2009 Al reinforced with 29 mu m SiCp, initial ageing consisted of GPB (Guinier Preston Baqaryatsky) I zone formation. Decreasing the particulate size to 4 mu m eliminated GPB I formation. This suppression of GPB I formation during ageing suggests that decreasing SiC size decreases the vacancy supersaturation following quenching by providing additional vacancy sinks at SiC/matrix interfaces. Subsequent ageing involved, at the larger reinforcement sizes, a transition with increasing time from GPB I zones to GPB Il-dislocation complexes. At smaller (4 mu m) reinforcement sizes, the formation of GPB Il-dislocation complexes occurs directly. Finally, the last stages of age hardening in all SiCp-reinforced composites examined consisted of heterogeneous nucleation of S'/S and GPB II --> S'/S transformation.

关键词： Metallic matrix composites

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Martensitic transformations in Ti-(16-26 at%) Nb alloys

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JOURNAL OF materials science 1996年第16期31卷 4267-4276页

作者： Ahmed, T Rack, HJ Materials Science and Engineering Program Department of Mechanical Engineering Clemson University Clemson USA

Martensitic phase transformations in the solution-treated and water-quenched binary Ti-Nb alloys in the range of 16-26 at % Nb, were examined. An ordered, base-centred orthorhombic martensite was observed for alloys containing up to 23.4 at % Nb. The substructure of this martensite was generally composed of twins and stacking faults, the presence of antiphase boundaries observed in the plates indicating that the martensite underwent ordering during quenching. Both order-disorder and NJ,temperatures were. observed to be affected by total interstitial content, higher contents increasing both temperatures. Increasing the niobium content to above 23.4% resulted in retention of the beta phase, this phase containing either athermal omega or ''diffuse'' omega depending upon niobium and total interstitial concentration. Finally, the microhardness of the Ti-Nb alloys examined was observed to decrease with increase in niobium and decrease in total interstitial content.

关键词： Titanium alloys

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Natural Alkaloids (Caffeine, Theobromine and Theophylline) as Dielectric Capping Layers for Gold and Aluminum Gate Electrodes in Low Operating Voltage Organic Field-Effect Transistors

IEEE Journal on Flexible Electronics

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IEEE Journal on Flexible Electronics 2025年

作者： Irimia, Cristian Vlad Yumusak, Cigdem Ban, Boyuan Leeb, Elisabeth Mayr, Felix Schimanofsky, Corina Mardare, Andrei Ionut Molnar, Maximilian Alexander Teichert, Christian Sariciftci, Niyazi Serdar Irimia-Vladu, Mihai Institute of Physical Chemistry Altenberger Str. 69 Linz4040 Austria Graz University of Technology in Graz Master of Science student in Advanced Materials Science program Austria Montanuniversität Leoben Chair of Physics Department of Physics Mechanics and Electrical Engineering Franz Josef Str. 18 Leoben8700 Austria Key Lab of Photovoltaic and Energy Conservation Materials Institute of Solid-State Physics Hefei Institute of Physical Science Hefei230031 China Altenberger Str. 69 Linz4040 Austria National Institute for Lasers Plasma and Radiation Physics Magurele077125 Romania

Three natural alkaloids: caffeine, theobromine and theophylline are reported for their application as dielectric layers in organic field effect transistors (OFETs) utilizing both gold and aluminum gate electrodes. After careful purification of the materials, a detailed analysis using x-ray diffraction spectroscopy (XRD), Fourier transform infrared spectroscopy (FTIR), contact angle (CA), impedance spectroscopy, amplitude modulated kelvin probe force microscope (AM-KPFM) and cyclic voltammetry (CV) is performed. OFET devices operating at typical voltages between 2 and 4 V have been fabricated with the investigated alkaloid films processed via blade coating (caffeine) or vacuum processing (theobromine and theophylline). The dielectric properties of these three alkaloids are measured in impedance spectroscopy and negligible leakage currents are observed when deposited in thin films as dielectric layers in OFETs on aluminum electrodes. There is a high tendency of these molecules to crystallize and form uneven surfaces. When the thin film forming properties are carefully controlled, organic alkaloids can be employed in applications involving implantable, transient or even edible electronics. © 2022 IEEE.

关键词： Fourier transform infrared spectroscopy

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When graphite meets Li metal

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National science Review 2020年第10期7卷 1521-1522页

作者： Yu Ding Guihua Yu Materials Science and Engineering Program and Department of Mechanical Engineering The University of Texas at Austin

Wetting, indicating the ability of a liquid to spread out over solid surfaces,is of vital importance in addressing the scientific issues related to energy and environment technologies. The study of wetting encompasses the academic disciplines of surface chemistry, nanotechnology, materials science and energy *** past several decades have witnessed significant progress in achieving desirable wetting performance with water,

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The effect of calcium and barium fluoride on CeF3 doped in gadolinium phosphate scintillating glass

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Ceramics International 2025年

作者： Sarumaha, C.S. Kantuptim, P. Yanagida, T. Intachai, N. Kothan, S. Kim, H.J. Busayaporn, W. Pakawanit, P. Phoovasawat, C. Kaewnuam, E. Kaewkhao, J. Faculty of Science and Technology Muban Chombueng Rajabhat University Ratchaburi 70150 Thailand Nakhon Pathom Rajabhat University Nakhon Pathom73000 Thailand Department of Materials Engineering Faculty of Engineering Kasetsart University Bangkok10900 Thailand Division of Materials Science of Science and Technology Nara Institute of Science and Technology 8916-5 Takayama Ikoma Nara630-0192 Japan Center of Radiation Research and Medical Imaging Department of Radiologic Technology Faculty of Associated Medical Sciences Chiang Mai University Chiang Mai50200 Thailand Department of Physics Kyungpook National University Daegu41566 Korea Republic of Synchrotron Research and Applications Division Synchrotron Light Research Institute 111 University Avenue Muang District Nakhon Ratchasima30000 Thailand Physics Program Faculty of Science and Technology Nakhon Pathom Rajabhat University Nakhon Pathom73000 Thailand

This study concerns alkaline fluorides such as CaF2 and BaF2 contained in gadolinium phosphate glass doped with CeF3, which were synthesized using a melt-quenching technique. Ce3+ was activated in both glasses and a comparative study of their optical, luminescence and scintillation behaviors was conducted. The results found that the higher atomic weight of BaF2 glass makes higher density compared with CaF2 glass, resulting in more integral scintillation efficiency. The quantum yield of BaF2-glass (PLZGdBafCe0.5) is also higher than that of CaF2-glass (PLZGdCafCe0.5). Energy transfer efficiency from Gd3+ to Ce3+ shows similar values, reflecting that the higher photoluminescence intensity of BaF2-glass comes from the efficiency of the luminescence center (Ce3+ ion). Photoluminescence and scintillation decay times were measured and found to be in the range of nanoseconds. XANES measurement was used to confirm the oxidation state and ratio between Ce3+/Ce4+. Moreover, the practical application of the glass scintillator was succeeded by micro-imaging using synchrotron X-ray. © 2025 Elsevier Ltd and Techna Group S.r.l.

关键词： Photoluminescence

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Macromolecule-Enriched Solvation Enabling High-Voltage Sodium-Ion Batteries

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Angewandte Chemie 2025年

作者： Zhiming Zhao Chen Liu Tianxing Lai Zehao Cui Arumugam Manthiram Materials Science and Engineering Program and Walker Department of Mechanical Engineering The University of Texas at Austin Austin TX 78712 USA

Sodium-ion batteries (SIBs) are emerging as a viable alternative for sustainable and cost-effective energy storage, yet their energy density is curtailed by relatively low voltage outputs (< 4 V) due to the lack of high-voltage electrolytes. Here, for the first time, we describe a high-voltage Na + electrolyte featuring a macromolecule-enriched solvation architecture. The vulnerable small molecules in the Na + solvation shell are replaced by macro polyamide (PA) molecules with high thermodynamic resilience, ensuring a wide electrochemical stability window for the electrolytes with suppressed oxidative/reductive decomposition. Concomitantly, the anions engage in H-bonding with the amido groups of PA, which not only stabilizes the anions against hydrolysis, but also delivers a high Na + transference number of 0.93. Importantly, the nitrogen-rich composition of the macromolecule-enriched electrolyte (MEE) fosters the formation of robust nitride interphases that impart enduring stability to both the cathode and anode. As a result, the hard carbon (HC) || NaNi 1/3 Fe 1/3 Mn 1/3 O 2 (NFM) full cells demonstrate significant rechargeability even with an ultrahigh cutoff voltage of 4.4 V. Our approach distinctively avoids the use of fluorinated molecules typically found in (localized-) high-concentration electrolytes, presenting a novel principle that could revolutionize high-voltage electrolyte design.

关键词： Hard carbon anode High-voltage electrolyte Layered oxide cathode Sodium-ion batteries Solvation structure

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2,5-Dimercapto-1,3,4-Thiadiazole(DMCT)-Based Polymers for Rechargeable Metal-Sulfur Batteries

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Energy & Environmental materials 2023年第6期6卷 283-290页

作者： Amruth Bhargav Arumugam Manthiram Materials Science and Engineering Program&Texas Materials Institute The University of Texas at AustinAustin Texas 78712USA

Organosulfur materials are a sustainable alternative to the present-day layered oxide cathodes in lithium-based *** such organosulfur material that was intensely explored from the 1990s to early 2010s is 2,5-dimercapto-1,3,4-thiadiazole(DMCT).However,research interest declined as the electrode reactions with DMCT were assumed to be too sluggish to be *** with the advances in metal-sulfur batteries,we revisit DMCT-based materials in the form of poly[tetrathio-2,5-(1,3,4-thiadiazole)],referred to as *** an appropriate choice of electrode design and electrolyte,pDMCT-S cathode paired with a Li-metal anode shows a capacity of 715 mA h g^(-1)and a Coulombic efficiency of 97.7%at a C/10 rate,thus quelling the concerns of sluggish ***,pDMCT-S shows significantly improved long-term cyclability compared to a sulfur *** into the origin of the stability reveals that the discharge product Li-DMCT in its mesomeric form can strongly bind to polysulfides,preventing their dissolution into the electrolyte and *** unique mechanism solves a critical problem faced by sulfur ***,this mechanism results in a stable performance of pDMCT-S with Na-metal cells as *** study opens the potential for exploring other organic materials that have inherent polysulfide sequestering capabilities,enabling long-life metal-sulfur batteries.

关键词： 2,5-dimercapto-1,3,4-thiadiazole electrochemistry metal-sulfur batteries organopolysulfide organosulfur batteries

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Deciphering the Impact of Polysulfide Solvation Structure on Electrical Double Layer Chemistry in Sodium–Sulfur Batteries

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Angewandte Chemie 2025年

作者： Weiqi Yao Min-Hao Pai Arumugam Manthiram Materials Science and Engineering Program & Walker Department of Mechanical Engineering The University of Texas at Austin Austin Texas 78712 USA

Room-temperature sodium–sulfur (RT Na–S) batteries are garnering attention for large-scale energy storage. However, their practical application is hindered by challenges, such as the shuttle effect of sodium polysulfides (NaPS) and dendrite growth. The high solubility of NaPS in the electrolyte is particularly problematic. It disrupts electron transfer and obstructs mass transport in the electrical double layer (EDL) region. The EDL plays a pivotal role in governing the interfacial chemistry between the electrode and electrolyte, significantly impacting the overall electrochemical performance. Through simulations and experimental screening of various solvents, including 1,2-dimethoxyethane (DME), tetrahydrofuran (THF), and tetrahydropyran (THP), along with ethyl 1,1,2,2-tetrafluoroethyl ether (ETFE) as a diluent, the relationship between NaPS solvation structure and EDL chemistry has been elucidated. Our findings reveal that THP-based localized high-concentration electrolyte (LHCE) not only reduces the solubility of NaPS by altering its solvation structure but also promotes the formation of a stable inorganic solid-electrolyte interphase (SEI) and improves compatibility with sodium metal. Consequently, Na–S batteries with LHCE-THP/ETFE exhibit long-term stability over 500 cycles at 1C rate with a capacity decay rate of only 0.07% per cycle. This study provides a methodology for designing electrolytes based on molecular structure, polysulfide solvation properties, and EDL interfacial chemistry.

关键词： Electrical double layer Electrolytes Polysulfide solvation structure Shuttle effect Sodium–sulfur batteries

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