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Impact of crystallinity on orbital torque generation in ferromagnets

Physical Review B 2024年第14期109卷 144412-144412页

作者： Riko Fukunaga Satoshi Haku Tenghua Gao Hiroki Hayashi Kazuya Ando Department of Applied Physics and Physico-Informatics Keio University Yokohama 223-8522 Japan Keio Institute of Pure and Applied Sciences Keio University Yokohama 223-8522 Japan State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China Center for Spintronics Research Network Keio University Yokohama 223-8522 Japan

We investigate the impact of crystallinity on the generation of orbital torques in Ni, which is predicted to exhibit the strongest orbital response among conventional 3d ferromagnetic metals. We show that the current-induced torques in Hf/Ni bilayers are primarily dominated by the orbital torque, arising from the orbital Hall effect in the Hf layer. We find that the orbital torque efficiency is enhanced by a factor of 2 when the stacking order of the Hf/Ni bilayer is altered. Through the examination of bulk and interfacial structural properties of the Ni and Hf layers, and by quantifying the torque efficiency in a symmetric Hf/Ni/Hf trilayer, we show that the orbital torque efficiency is strongly dependent on the crystallinity of the Ni layer. This dependence is in stark contrast to conventional spin-orbit torques, which arise from the spin Hall effect and are typically insensitive to the crystallinity of the ferromagnetic layer. These findings highlight the significant role of the crystalline structure of the ferromagnetic layer in its orbital response and illustrate the potential of crystal structure engineering in optimizing orbital torques.

关键词： Magnetization dynamics Spin current Spin-orbit coupling Spin-orbit torque Spintronics

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Piezoelectric ceramics with high piezoelectricity and broad temperature usage range

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Journal of Materiomics 2021年第4期7卷 683-692页

作者： Qinghu Guo Fei Li Fangquan Xia Pengbin Wang Xiaoyi Gao Hua Hao Hanxing Liu Huajun Sun Shujun Zhang State Key Laboratory Silicate Materials for Architectures Center for Smart Materials and Device IntegrationSchool of Materials Science and EngineeringWuhan University of TechnologyWuhan430070China Electronic Materials Research Laboratory Key Laboratory of the Ministry of EducationXi’an Jiaotong UniversityXi’an710049China School of Chemistry and Chemical Engineering University of JinanJinan250022China Institute for Superconducting and Electronic Materials Australian Institute of Innovative MaterialsUniversity of WollongongNew South Wales2500Australia State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and EngineeringWuhan University of TechnologyWuhan430070China

There is a general observation that the Curie temperature and piezoelectric property of the ferroelectric ceramics can be enhanced only at the expense of each other,i.e.,higher piezoelectricity,lower Curie temperature,thus,limits their applications over broad temperature *** this research,Sm-modified 0.15 Pb(Mg_(1/3)Nb_(2/3))O_(3)-(0.85-x)PbZrO_(3)-xPbTiO_(3) ceramics have been studied,where excellent piezoelectric coefficients d33¼720 pC/N,d_(33)*=950 pm/V and high Curie temperature T_(C)=293℃ were simultaneously achieved for x=0.42 composition by designing the morphotropic phase boundary(MPB)with local structural *** particular significance is that a high thermal stability was observed with piezoelectric variation below 20%with temperature up to 280℃,demonstrating that the x=0.42 composition is a good candidate for piezoelectric application over broad temperature range where high temperature stability is *** work provides a good paradigm for designing highperformance piezoelectric ceramics with high thermal stability via a combination of MPB and local structural heterogeneity.

关键词： Piezoelectric ceramics Local structural heterogeneity Electromechanical response Thermal stability

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Correction: Duetting electronic structure modulation of Ru atoms in RuSe2@NC enables more moderate H* adsorption and water dissociation for hydrogen evolution reaction

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Journal of materials Chemistry A 2022年第18期10卷 10242-10243页

作者： Ding Chen Ruihu Lu Youtao Yao Dulan Wu Hongyu Zhao Ruohan Yu Zonghua Pu Pengyan Wang Jiawei Zhu Jun Yu Pengxia Ji Zongkui Kou Haolin Tang Shichun Mu State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China Foshan Xianhu Laboratory Foshan 528200 China State Key Laboratory of Silicate Materials for Architectures International School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 China

Correction for ‘Duetting electronic structure modulation of Ru atoms in RuSe2@NC enables more moderate H* adsorption and water dissociation for hydrogen evolution reaction’ by Ding Chen et al., J. Mater. Chem. A, 20...

Correction for ‘Duetting electronic structure modulation of Ru atoms in RuSe₂@NC enables more moderate H* adsorption and water dissociation for hydrogen evolution reaction’ by Ding Chen et al., J. Mater. Chem. A, 2022, 10, 7637–7644, https://***/10.1039/d2ta01032a.

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Rationally Designing Anti-Poisoning Polymer Electrolyte by Electronegativity Modulation: Towards Efficient Ammonia-Cracked Hydrogen Fuel Cells

SSRN

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SSRN 2023年

作者： Shuai, Jiaqi Zhao, Shengqiu Liao, Yucong Wu, Fanglin Wang, Rui Wang, Letian Shen, Chunhui Tang, Haolin State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Department of Polymer Materials & Engineering School of Material Science & Engineering Wuhan University of Technology Wuhan430070 China Hubei Key Laboratory of Fuel Cells Wuhan University of Technology Wuhan430070 China

Ammonia as a hydrogen enrichment medium has tremendous advantages over pure hydrogen in terms of transportation and utilization. The high-efficiency anti-ammonia-poisoning membrane electrode assembly (MEA) is pivotal for the practical implementation of ammonia-resistant proton exchange membrane fuel cells (PEMFCs). As for the polymer electrolyte, which is an integral part of the proton exchange membrane (PEM) and catalytic layer (CL) binder in the MEA, structural design is an effective way to improve its resistance to ammonia poisoning. Herein, an in-depth study of sulfonimides with superacidic structures reveals that the proton dissociation energies can be altered by tuning the terminal groups with different electronegativity and enhancing the competitive adsorption of protons on Pt. Four perfluorinated backbone sulfonimides (PFSI-x (x= TSM, MSA, ESA, and iPSA)) with distinct charge delocalization were fabricated by grafting different electronegative monomers onto the perfluorosulfonyl fluoride (PFSF). The results show that PFSI-TSM possesses a higher electrostatic potential (2.69 eV) and the lowest activation energy (12.07 KJ/mol). Meanwhile, the performance of the PFSI-TSM PEM fuel cell is 40.6% higher than the PFSA at 80°C, 100% relative humidity (RH) under 100 ppm NH3, with a maximum power density of 635.2 mW/cm2. The underlying reason for enhanced performance is in virtue of the more electronegative end groups render the superacid electrolyte with higher acidity and pKa values, which change the direction of the acid dissociation equilibrium reaction on the Pt surface, enhance the competitive adsorption of protons in the MEA and reduces the probability of ammonia adsorption poisoning. The insights in charge delocalization and proton ionization construct the structure-property relationship which would provide the guidance for a rational design of PEM for ammonia-resistant fuel cells. © 2023, The Authors. All rights reserved.

关键词： Electronegativity

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Minimizing tin(Ⅱ) oxidation using ethylhydrazine oxalate for high-performance all-perovskite tandem solar cells

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Journal of Semiconductors 2025年第5期 91-98页

作者： Jianhua Zhang Xufeng Liao Weisheng Li Yutian Tian Qinyang Huang Yitong Ji Guotang Hu Qingguo Du Wenchao Huang Donghoe Kim Yi-Bing Cheng Jinhui Tong State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology School of Art and Design Wuhan University of Technology School of Information Engineering Wuhan University of Technology Department of Materials Science and Engineering Korea University Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory

All-perovskite tandem solar cells（ATSCs） have the potential to surpass the Shockley-Queisser efficiency limit of conventional single-junction devices. However, the performance and stability of mixed tin–lead（Sn–Pb） perovskite solar cells（PSCs）, which are crucial components of ATSCs, are much lower than those of lead-based perovskites. The primary challenges include the high crystallization rate of perovskite materials and the susceptibility of Sn2+oxidation, which leads to rough morphology and unfavorable p-type self-doping. To address these issues, we introduced ethylhydrazine oxalate（EDO） at the perovskite interface, which effectively inhibits the oxidation of Sn2+and simultaneously enhances the crystallinity of the perovskite. Consequently, the EDO-modified mixed tin-lead PSCs reached a power conversion efficiency（PCE） of 21.96% with high reproducibility. We further achieved a 27.58% efficient ATSCs by using EDO as interfacial passivator in the Sn-Pb PSCs.

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Eutectic Electrolyte with Unique Solvation Structure for High-Performance Zinc-Ion Batteries (vol 62, 10.1002/anie.202303744, 2023)

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ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 2023年第22期62卷 e202206717-e202206717页

作者： Geng, L. Meng, J. Wang, X. Han, C. Han, K. Xiao, Z. Huang, M. Xu, P. Zhang, L. Zhou, L. Mai, L. State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 P. R. China Department of Physical Science & Technology School of Science Wuhan University of Technology Wuhan 430070 P. R. China Hubei Longzhong Laboratory Xiangyang 441000 P. R. Hubei China

Zinc-ion batteries (ZIB) present great potential in energy storage due to low cost and high safety. However, the poor stability, dendrite growth, and narrow electrochemical window limit their practical application. Herein, we develop a new eutectic electrolyte consisting of ethylene glycol (EG) and ZnCl2 for dendrite-free and long-lifespan ZIBs. The EG molecules participate in the Zn2+ solvation via coordination and hydrogen-bond interactions. Optimizing the ZnCl2/EG molar ratio (1 : 4) can strengthen intermolecular interactions to form [ZnCl(EG)]+ and [ZnCl(EG)2]+ cations. The dissociation–reduction of these complex cations enables the formation of a Cl-rich organic–inorganic hybrid solid electrolyte interphase film on a Zn anode, realizing highly reversible Zn plating/stripping with long-term stability of ≈3200 h. Furthermore, the polyaniline||Zn cell manifests decent cycling performance with ≈78 % capacity retention after 10 000 cycles, and the assembled pouch cell demonstrates high safety and stable capacity. This work opens an avenue for developing eutectic electrolytes for high-safety and practical ZIBs.

关键词： Deep Eutectic Solvents Dendrite-Free Zn Anodes Eutectic Electrolytes Solvation Structure Zinc-Ion Batteries

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Long lifespan Li-Se battery: Advances, challenges and prospects

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Journal of Energy Chemistry 2025年 102卷 712-733页

作者： Hongyan Li Thomas L. Madanu Tarek Barakat Wen-Da Dong Alexandru Vlad Xikun Zhang Cheng-Bin Jin Yu Li Bao-Lian Su College of Materials and Chemistry China Jiliang University Hangzhou 310018 Zhejiang China Laboratory of Inorganic Materials Chemistry (CMI) Namur Institute of Structured Matter (NISM) University of Namur 61 rue de Bruxelles B-5000 Namur Belgium State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430074 Hubei China Institute of Condensed Matter and Nanosciences Molecular Chemistry Materials and Catalysis Université catholique de Louvain Louvain-la-Neuve Belgium

Lithium-selenium (Li-Se) batteries have attracted increasing attention as one of the next-generation battery systems due to much higher electronic conductivity and comparable volumetric capacity of Se compared to the popular sulfur cathode. However, its practical application still faces great challenges, especially the rapid capacity decay triggered by the loss of active Se species. A comprehensive review to uncover the in-depth failure mechanism and provide targeted solutions to promote the stable operation of Li-Se batteries is urgently needed. This review systematically summarizes the strategies in the new perspective, focusing on the optimization of Se utilization in Li-Se batteries by keeping a high Se maintenance in the cathode and accelerating the electrochemical kinetics of lithium polyselenides (LiPSe) conversion. On the basis of structural design and Li 2 Se active material introduction to accommodate volume expansion, blocking shuttle transport of LiPSe by physical/chemical adsorption, bonding Se with polymers or cathode electrolyte interphase (CEI) construction, and catalytic design to accelerate the conversion of LiPSe, different strategies for improving the utilization of Se have been evaluated and discussed. To address the inevitable loss of Se, prospects on inactive Se reactivation and Li protection are detailedly proposed and analyzed referring to the chemistry and corrosion science. Additionally, the perspectives on the future design and comprehensive parameter evaluations for the optimization of Li-Se batteries are recommended. This review comprehensively explains the causes and solutions of capacity fading and provides potential efforts for lifespan expansion of batteries, shedding light on the future development of Li-Se batteries.

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Stable perovskite solar cells with efficiency of 22.6%via quinoxaline-based polymeric hole transport material

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Science China Chemistry 2021年第11期64卷 2035-2044页

作者： Chenxing Lu Can Zhu Lei Meng Chenkai Sun Wenbin Lai Shucheng Qin Jinyuan Zhang Wenchao Huang Jiaqi Du Yiyang Wang Yongfang Li Beijing National Laboratory for Molecular Sciences CAS Key Laboratory of Organic SolidsInstitute of ChemistryChinese Academy of SciencesBeijing100190China School of Chemical Science University of Chinese Academy of SciencesBeijing100049China College of Chemistry Green Catalysis CenterZhengzhou UniversityZhengzhou450001China Department of Materials Science and Engineering Monash UniversityClaytonVIC3168Australia State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan430070China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen ValleyFoshan528216China Laboratory of Advanced Optoelectronic Materials College of ChemistryChemical Engineering and Materials ScienceSoochow UniversitySuzhou215123China

Poor stability of spiro-OMe TAD hole transport materials(HTMs)with dopant is a major obstacle for the commercialization of perovskite solar cells(pero-SCs).Herein,we demonstrate a series of quinoxaline-based D-A copolymers PBQ5,PBQ6 and PBQ10 as the dopant-free polymer HTMs for high performance *** D-A copolymers are composed of fluorothienyl benzodithiophene(BDTT)as D-unit,difluoroquinoxaline(DFQ)with different side chains as A-unit,and thiophene asπ-bridge,where the side chains on the DFQ unit are bi-alkyl for PBQ5,bi-alkyl-fluorothienyl for PBQ6,and alkoxyl for *** the three copolymers are adopted as the dopant-free HTM in the *** planar n-i-p structured pero-SCs based on(FAPb I_(3))_(0.98)(MAPb Br_(3))_(0.02)with PBQ6 HTM demonstrated the high power conversion efficiency(PCE)of 22.6%with Vocof1.13 V and FF of 80.8%,which is benefitted from the suitable energy level and high hole mobility of *** PCE of 22.6%is the highest efficiency reported in the n-i-p structured pero-SCs based on dopant-free D-A copolymer *** addition,the peroSCs show significantly enhanced ambient,thermal and light-soaking stability compared with the devices with traditional spiroOMe TAD HTM.

关键词： perovskite solar cells hole transport materials D-A copolymer difluoroquinoxaline stability

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Carbon decorated Li_(3)V_(2)(PO_(4))_(3) for high-rate lithium-ion batteries:Electrochemical performance and charge compensation mechanism

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Journal of Energy Chemistry 2021年第2期30卷 124-131,I0005页

作者： Manling Ding Chen Cheng Qiulong Wei Yue Hu Yingying Yan Kehua Dai Jing Mao Jinghua Guo Liang Zhang Liqiang Maig Institute of Functional Nano&Soft Materials(FUNSOM) Jiangsu Key Laboratory for Carbon-Based Functional Materials&1 DevicesSoochow UniversitySuzhou 215123JiangsuChina Department of Materials Science and Engineering Fujian Key Laboratory of Materials GenomeCollege of MaterialsXiamen UniversityXiamen 361005FujianChina College of Chemistry Tianjin Normal UniversityTianjin 300387China School of Materials Science and Engineering Zhengzhou UniversityZhengzhou 450001HenanChina Advanced Light Source Lawrence Berkeley National LaboratoryBerkeleyCA 94720United States Department of Chemistry and Biochemistry University of CaliforniaSanta CruzCA 95064United States State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and EngineeringWuhan University of Technology.Wuhan 430070HubeiChina

Fast charging and high-power delivering batteries are highly demanded in mobile electronics,electric vehicles and grid energy storage,but there are full of *** star-material Li_(3)V_(2)(PO_(4))_(3) is demonstrated as a promising high-rate cathode material meeting the above ***,we report the carbon decorated Li_(3)V_(2)(PO_(4))_(3) (LVP/C) cathode prepared via a facile method,which displays a remarkable high-rate capability and long-term cycling ***,the prepared LVP/C delivers a high discharge capacity of 122 mAh g^(-1)(-93% of the theoretical capacity) at a high rate up to 20 C and a superior capacity retention of 87.1% after 1000 ***,by applying a combination of X-ray absorption spectroscopy and full-range mapping of resonant inelastic X-ray scattering,we clearly elucidate the structural and chemical evolutions of LVP upon various potentials and cycle *** show unambiguous spectroscopic evidences that the evolution of the hybridization strength between V and O in LVP/C as a consequence of lithiation/delithiation is highly reversible both in the bulk and on the surface during the discharge-charge processes even over extended cycles,which should be responsible for the remarkable electrochemical performance of LVP/*** present study provides not only an effective synthesis strategy but also deeper insights into the surface and bulk electrochemical reaction mechanism of LVP,which should be beneficial for the further design of high-performance LVP electrode materials.

关键词： Lithium-ion batteries Li_(3)V_(2)(PO_(4))_(3) Charge compensation mechanism X-ray absorption spectroscopy Resonant inelastic X-ray scattering

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High-throughput data-driven interface design of high-energy-density polymer nanocomposites

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Journal of Materiomics 2020年第3期6卷 573-581页

作者： Zhong-Hui Shen Yang Shen Xiao-Xing Cheng Han-Xing Liu Long-Qing Chen Ce-Wen Nan State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Center of Smart Materials and DevicesWuhan University of TechnologyWuhan430070China School of Materials Science and Engineering State Key Lab of New Ceramics and Fine ProcessingTsinghua UniversityBeijing100084China Department of Materials Science and Engineering The Pennsylvania State UniversityUniversity ParkPA16802United States

Understanding the interface effect in dielectric nanocomposites is crucial to the enhancement of their *** this work,a data-driven interface design strategy based on high-throughput phase-field simulations is developed to study the interface effect and then optimize the permittivity and breakdown strength of ***,we use two microscopic features that are closely related to the macroscopic dielectric properties,the thickness and permittivity of the interface phases,to evaluate the role of interfaces in experimental configuration,and thus provide quantitative design schemes for the interfacial *** the polyvinyl difluoride(PVDF)-BaTiO_(3) nanocomposite as an example,the calculation results demonstrate that the interfacial polarization could account for up to 83.6% of the increase in the experimentally measured effective permittivity of the *** on the interface optimized strategy,a maximum enhancement of ~156% in the energy density could be achieved by introducing an interface phase with d/r=0.55 and ε_(interface)/ε_(filler)=0:036,compared to the pristine ***,the present work not only provides fundamental understanding of the interface effect in dielectric nanocomposites,but also establishes a powerful data-driven interface design framework for such materials that could also be easily generalized and applied to study interface issues in other functional nanocomposites,such as solid electrolytes and thermoelectrics.

关键词： Interface Polymer nanocomposites Energy storage Data-driven Phase-field simulation

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