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Publisher Correction: Operando monitoring the lithium spatial distribution of lithium metal anodes

Nature communications 2018年第1期9卷 2902页

作者： Shasha Lv Tomas Verhallen Alexandros Vasileiadis Frans Ooms Yaolin Xu Zhaolong Li Zhengcao Li Marnix Wagemaker Department of Radiation Science and Technology Delft University of Technology Mekelweg 15 Delft 2629 JB The Netherlands. The State Key Laboratory of New Ceramics and Fine Processing School of Materials Science and Engineering Tsinghua University Beijing 100084 China. Key Laboratory of Advanced Materials (MOE) School of Materials Science and Engineering Tsinghua University Beijing 100084 China. Department of Radiation Science and Technology Delft University of Technology Mekelweg 15 Delft 2629 JB The Netherlands. m.wagemaker@tudelft.nl.

The original HTML version of this Article omitted to list Zhengcao Li as a corresponding author. Correspondingly, the original PDF version of this Article incorrectly stated that 'Correspondence and requests for materials should be addressed to M.W. (email: ***@***)', instead of the correct 'Correspondence and requests for materials should be addressed to Z.L. (email: zcli@***) or to M.W. (email: ***@***)'. This has been corrected in both the PDF and HTML versions of the Article.

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Translational plasma stomatology:applications of cold atmospheric plasmas in dentistry and their extension

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High Voltage 2017年第3期2卷 188-199页

作者： He-Ping Li Xiao-Fei Zhang Xiao-Ming Zhu Miao Zheng Shu-Fang Liu Xuan Qi Kai-Peng Wang Jian Chen Xiao-Qing Xi Jian-Guo Tan Kostya(Ken)Ostrikov Department of Engineering Physics Tsinghua UniversityBeijing 100084People's Republic of China Department of Prosthodontics Peking University School and Hospital of StomatologyBeijing 100081People's Republic of China Department of Stomatology Peking University Third HospitalBeijing 100191People's Republic of China Department of Pediatrics First Hospital of Tsinghua UniversityBeijing 100016People's Republic of China College of Mechanical Engineering North China University of Science and TechnologyTangshanHebei 063009People's Republic of China State Key Laboratory of New Ceramics and Fine Processing School of Materials Science and EngineeringTsinghua UniversityBeijing 100084People's Republic of China School of Chemistry Physics and Mechanical EngineeringQueensland University of TechnologyBrisbaneQueensland 4000Australia CSIRO-QUT Joint Sustainable Materials and Processes Laboratory Commonwealth Scientific and Industrial Research OrganisationPO Box 218LindfieldNSW 2070Australia

In recent years,translational plasma medicine(TPM),as a novel application area of plasmas,has attracted much attention of experts from both academic and clinical ***-of-the-art of the lab-scale research and clinical trials of the cold atmospheric plasmas(CAPs)in the stomatology are reviewed in detail from the direct and indirect applications of the *** on the discussions concerning the relationship between the plasma stomatology and the plasma medicine,it is indicated that it would be an important reference for promoting the TPM starting from the fundamental and application studies in the field of dentistry,which is also one of the most three promising application fields of plasma medicine.

关键词： plasmas starting discussions

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Erratum to: Search for dark matter produced in association with a leptonically decaying Z boson in proton–proton collisions at s = 13 Te

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The European Physical Journal C 2021年第4期81卷 1-16页

作者： A. M. Sirunyan A. Tumasyan W. Adam T. Bergauer M. Dragicevic J. Erö A. Escalante Del Valle R. Frühwirth M. Jeitler N. Krammer L. Lechner D. Liko T. Madlener I. Mikulec F. M. Pitters N. Rad J. Schieck R. Schöfbeck M. Spanring S. Templ W. Waltenberger C.-E. Wulz M. Zarucki V. Chekhovsky A. Litomin V. Makarenko J. Suarez Gonzalez M. R. Darwish E. A. De Wolf D. Di Croce X. Janssen T. Kello A. Lelek M. Pieters H. Rejeb Sfar H. Van Haevermaet P. Van Mechelen S. Van Putte N. Van Remortel F. Blekman E. S. Bols S. S. Chhibra J. D’Hondt J. De Clercq D. Lontkovskyi S. Lowette I. Marchesini S. Moortgat A. Morton Q. Python S. Tavernier W. Van Doninck P. Van Mulders D. Beghin B. Bilin B. Clerbaux G. De Lentdecker B. Dorney L. Favart A. Grebenyuk A. K. Kalsi I. Makarenko L. Moureaux L. Pétré A. Popov N. Postiau E. Starling L. Thomas C. Vander Velde P. Vanlaer D. Vannerom L. Wezenbeek T. Cornelis D. Dobur M. Gruchala I. Khvastunov M. Niedziela C. Roskas K. Skovpen M. Tytgat W. Verbeke B. Vermassen M. Vit G. Bruno F. Bury C. Caputo P. David C. Delaere M. Delcourt I. S. Donertas A. Giammanco V. Lemaitre K. Mondal J. Prisciandaro A. Taliercio M. Teklishyn P. Vischia S. Wuyckens J. Zobec G. A. Alves C. Hensel A. Moraes W. L. Aldá Júnior E. Belchior Batista Das Chagas H. BRANDAO MALBOUISSON W. Carvalho J. Chinellato E. Coelho E. M. Da Costa G. G. Da Silveira D. De Jesus Damiao S. Fonseca De Souza J. Martins D. Matos Figueiredo M. Medina Jaime C. Mora Herrera L. Mundim H. Nogima P. Rebello Teles L. J. Sanchez Rosas A. Santoro S. M. Silva Do Amaral A. Sznajder M. Thiel F. Torres Da Silva De Araujo A. Vilela Pereira C. A. Bernardes L. Calligaris T. R. Fernandez Perez Tomei E. M. Gregores D. S. Lemos P. G. Mercadante S. F. Novaes Sandra S. Padula A. Aleksandrov G. Antchev I. Atanasov R. Hadjiiska P. Iaydjiev M. Misheva M. Rodozov M. Shopova G. Sultanov M. Bonchev A. Dimitrov T. Ivanov L. Litov B. Pavlov P. Petkov A. Petrov W. Fang Q. Guo H. Wang L. Yuan M. Ahmad Z. Hu Y. Wang E. Chapon G. M. Chen H. S. Chen M. Chen A. Kapoor D. Leggat H. Yerevan Physics Institute Yerevan Armenia Institut für Hochenergiephysik Vienna Austria Vienna University of Technology Vienna Austria Institute for Nuclear Problems Minsk Belarus Universiteit Antwerpen Antwerpen Belgium Department of Basic and Applied Sciences Faculty of Engineering Arab Academy for Science Technology and Maritime Transport Alexandria Egypt Université Libre de Bruxelles Bruxelles Belgium Vrije Universiteit Brussel Brussel Belgium Ghent University Ghent Belgium IRFU CEA Université Paris-Saclay Gif-sur-Yvette France Université Catholique de Louvain Louvain-la-Neuve Belgium Centro Brasileiro de Pesquisas Fisicas Rio de Janeiro Brazil Universidade do Estado do Rio de Janeiro Rio de Janeiro Brazil Universidade Estadual de Campinas Campinas Brazil Federal University of Rio Grande do Sul Porto Alegre Brazil UFMS Nova Andradina Brazil Universidade Federal de Pelotas Pelotas Brazil Universidade Estadual Paulista Universidade Federal do ABC São Paulo Brazil Institute for Nuclear Research and Nuclear Energy Bulgarian Academy of Sciences Sofia Bulgaria University of Sofia Sofia Bulgaria Beihang University Beijing China Department of Physics Tsinghua University Beijing China Institute of High Energy Physics Beijing China University of Chinese Academy of Sciences Beijing China State Key Laboratory of Nuclear Physics and Technology Peking University Beijing China Sun Yat-Sen University Guangzhou China Institute of Modern Physics and Key Laboratory of Nuclear Physics and Ion-beam Application (MOE) - Fudan University Shanghai China Zhejiang University Hangzhou China Universidad de Los Andes Bogota Colombia Universidad de Antioquia Medellin Colombia University of Split Faculty of Electrical Engineering Mechanical Engineering and Naval Architecture Split Croatia University of Split Faculty of Science Split Croatia Institute Rudjer Boskovic Zagreb Croatia Institute for Theoretical and Experimental Physics named by A.I. Alikhanov of NRC ‘K

A Correction to this paper has been published: https://***/10.1140/epjc/s10052-020-08739-5

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Superconductivity of LaH10and LaH16: new twists of the story

arXiv

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arXiv 2018年

作者： Kruglov, Ivan A. Semenok, Dmitrii V. Song, Hao Szczȩśniak, Radoslaw Wrona, Izabela A. Akashi, Ryosuke Esfahani, M. Mahdi Davari Duan, Defang Cui, Tian Kvashnin, Alexander G. Oganov, Artem R. Moscow Institute of Physics and Technology 9 Institutsky lane Dolgoprudny141700 Russia Moscow127055 Russia Skolkovo Institute of Science and Technology Skolkovo Innovation Center 3 Nobel Street Moscow121205 Russia Institute of Physics Jan Dlugosz University in Czestochowa Ave. Armii Krajowej 13/15 Czestochowa42-200 Poland Institute of Physics Czestochowa University of Technology Ave. Armii Krajowej 19 Czestochowa42-200 Poland University of Tokyo 7-3-1 Hongo Bunkyo Tokyo113-8654 Japan Department of Geosciences Center for Materials by Design Institute for Advanced Computational Science State University of New York Stony BrookNY11794-2100 United States International Center for Materials Discovery Northwestern Polytechnical University Xi'an710072 China Key State Laboratory of Superhard Materials Jilin University Changchun China

Recent experiments have established previously predicted LaH10as the highesttemperature superconductor, with TCup to 250-260 K [1]. In this work we explore the highpressure phase stability and superconductivity of lanthanum hydrides LaHm. We predict the stability of a hitherto unreported polyhydride P 6/mmm-LaH16at pressures above 150 GPa;at 200 GPa its predicted superconducting TCis 156 K, critical field μ0HC(0) ∼ 35 T and superconducting gap is up to 35 meV. We revisit the superconductivity of LaH10and find its TCto be up to 259 K at 170 GPa from solving the Eliashberg equation and 271 K from solving the gap equation in SCDFT, which also allowed us to compute the Coulomb pseudopotential μ∗for LaH10and LaH16. The presence of several polymorphic modifications of LaH10may explain the variety in its measured TCvalues [1,2]. Copyright © 2018, The Authors. All rights reserved.

关键词： Lanthanum compounds

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Electrochemical Double‐Layer Capacitor Energized by Adding an Ambipolar Organic Redox Radical into the Electrolyte

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Angewandte Chemie 2018年第27期130卷

作者： Lintong Hu Chao Shi Kai Guo Tianyou Zhai Huiqiao Li Yonggang Wang State Key Laboratory of Material Processing and Die & Mould Technology School of Materials Science and Engineering Huazhong University of Science and Technology Wuhan 430074 P. R. China Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials Institute of New Energy iChEM (Collaborative Innovation Center of Chemistry for Energy Materials) Fudan University Shanghai 200433 P. R. China

Carbon‐based electrochemical double‐layer capacitors (EDLCs) generally exhibit high power and long life, but low energy density/capacitance. Pore/morphology optimization and pseudo‐capacitive materials modification of carbon materials have been used to improve electrode capacitance, but leading to the consumption of tap density, conductivity and stability. Introducing soluble redox mediators into electrolyte is a promising alternative to improve the capacitance of electrode. However, it is difficult to find one redox mediator that can provide additional capacitance for both positive and negative electrodes simultaneously. Here, an ambipolar organic radical, 2, 2, 6, 6‐tetramethylpiperidinyloxyl (TEMPO) is first introduced to the electrolyte, which can substantially contribute additional pseudo‐capacitance by oxidation at the positive electrode and reduction at the negative electrode simultaneously. The EDLC with TEMPO mediator delivers an energy density as high as 51 Wh kg −1 , 2.4 times of the capacitor without TEMPO, and a long cycle stability over 4000 cycles. The achieved results potentially point a new way to improve the energy density of EDLCs.

关键词： Ambipolare Redoxmediatoren Energiespeicherung Organische Radikale Redoxaktive Elektrolyte Superkondensatoren

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Aerodynamic levitated laser annealing method to defective titanium dioxide with enhanced photocatalytic performance

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Nano Research 2016年第12期9卷 3839-3847页

作者： Hehe Wei Xiaoguang Ma Liu Gu Jianqiang Li Wenjie Si Gang OU Wen Yu Chunsong Zhao Jiaying Li Mingjun Song Zhijian Peng Hui Wu State Key Laboratory of New Ceramics and Fine Processing School of Materials Science and Engineering Tsinghua University Beijing 100084 China National Engineering Laboratory for Hydrometallurgical Cleaner Production Technology Key Laboratory of Green Process and Engineering Institute of Process Engineering Chinese Academy of Sciences Beijing 100190 China School of Engineering and Technology China University of Geosciences Beijing 100083 China Department of Chemistry and Collaborative Innovation Center for Nanomatefial Science and Engineering Tsinghua University Beijing 100084 China

Defective TiO2 has attracted increasing attention for use in photocatalytic and electrochemical materials because of its narrowed band-gap and improved visible-light photocatalytic activity. However, a facile and efficient approach for obtaining defect-rich TiO2 still remains a challenge. Herein, we demonstrate such an approach to narrow its bandgap and improve visible-light absorption through implanting abundant defects by aerodynamic levitated laser annealing （ALLA） treatment. Note that the ALLA method not only provides rapid annealing, solidifying and cooling process, but also exhibits high efficiency for homogeneous and defective TiO2 nanoparticles. The laser-annealed TiO2 achieves a high hydrogen evolution rate of 8.54 mmol.h-1.g-1, excellent decomposition properties within 60 min, and outstanding recyclability and stability, all of which are superior to the corresponding properties of commercial P25.

关键词： hydrogen evolution TiO2 photocatalyst laser annealing

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Li–O2Batteries: Interfacial Super‐Assembled Porous CeO2/C Frameworks Featuring Efficient and Sensitive Decomposing Li2O2for Smart Li–O2Batteries (Adv. Energy Mater. 40/2019)

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advanced Energy materials 2019年第40期9卷

作者： Yue Hou Jun Wang Jiaqing Liu Chuanxin Hou Zhaohong Xiu Yuqi Fan Lanling Zhao Yanjie Zhai Hongyu Li Jie Zeng Xiang Gao Shan Zhou Dongwei Li Yong Li Feng Dang Kang Liang Pu Chen Changming Li Dongyuan Zhao Biao Kong Department of Chemistry Shanghai Key Lab of Molecular Catalysis and Innovative Materials iChEM Fudan University Shanghai 200433 P. R. China Key Laboratory for Liquid‐Solid Structural Evolution and Processing of Materials (Ministry of Education) Shandong University Jinan 250061 P. R. China National Supercomputer Research Center of Advanced Materials Advanced Materials Institute Qilu University of Technology Shandong Academy of Sciences Jinan 250014 P. R. China Institute of Environment and Ecology Shandong Normal University Jinan 250014 P. R. China School of Physics Shandong University Jinan 250100 P. R. China School of Chemical Engineering and Graduate School of Biomedical Engineering The University of New South Wales Sydney NSW 2052 Australia Department of Chemical Engineering University of Waterloo Waterloo Ontario N2L 3G1 Canada Institute for Clean Energy and Advanced Materials Southwest University Chongqing 400715 P. R. China

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First-Principles Study on Hexagonal WO_3 for HCHO Gas Sensing Application

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Acta Metallurgica Sinica(English Letters) 2015年第6期28卷 772-780页

作者： Bo-Lin Tang Guo-Hua Jiang Wen-Xing Chen Jun-Min Wan Department of Materials Engineering Zhejiang Sci-Tech University Key Laboratory of Advanced Textile Materials and Manufacturing Technology (ATMT) Ministry of Education National Engineering Laboratory for Textile Fiber Materials and Processing Technology (Zhejiang)

The adsorption energy, electronic structure, density of states, and electron population for adsorption of HCHO on the hexagonal WO3 （h-WO3）（001） surfaces were investigated by density functional theory calculations. The adsorption energy of HCHO molecule on W and O sites of WO-terminated h-WO3 （001） surface was -0.309 and -0.432 eV compared with the value at -1.936 eV for HCHO molecule on O-terminated h-WO3 （001） surface. According to the calculated results, the adsorption of HCHO on h-WO3 （001） surface was spontaneous with physical adsorption on WO- terminated h-WO3 （001） surface and chemisorption on O-terminated h-WO3 （001） surface. The charge transfer from adsorbed HCHO molecule to WO3 （001） surface was confirmed by the Mulliken population analysis, which suggested the potential application of h-WO3 for HCHO gas detection.

关键词： Semiconductors Surfaces Crystal structure Electronic structure

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Preparation of Mesoporous Bi_4(GeO_4)_3 Microspheres from Na_4Ge_9O_(20) Template Microspheres for Photodegradation of Reactive Brilliant Red X-3B

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Acta Metallurgica Sinica(English Letters) 2015年第9期28卷 1156-1161页

作者： Hua Chen Guo-Hua Jiang Yong-Kun Liu Lei Li Qin Huang Wen-Xing Chen Department of Materials Engineering Zhejiang Sci-Tech University National Engineering Laboratory for Textile Fiber Materials and Processing Technology (Zhejiang) Key Laboratory of Advanced Textile Materials and Manufacturing Technology (ATMT) Ministry of Education

Mesoporous materials have attracted increasing attention due to their wide application. In this paper, the Na4Ge9020 microspheres were firstly prepared by solvothermal method. Then, the as-prepared Na4Ge9020 microspheres were dispersed into Bi（NO3）3 solution, and the Bi4（GeO4）3 microspheres with mesoporous structure were formed due to the solid-state reaction between bismuth nitrate and Na4Ge9020. The morphology, structure and optical properties were characterized by SEM, EDS, XRD, FITR, BET and UV-Vis diffuse reflectance analysis. The as-prepared products exhibited excellent photocatalytic performance for degradation of reactive brilliant red X-3B under the UV light irradi- ation. A possible photocatalytic mechanism was discussed as well.

关键词： Mesoporous Microspheres Photocatalysis

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Contrasting room-temperature hydrogen sensing capabilities of Pt-SnO2 and Pt-TiO2 composite nanoceramics

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Nano Research 2016年第11期9卷 3528-3535页

作者： Yao Xiong Wanping Chen Yesheng Li Ping Cui Shishang Guo Wei Chen Zilong Tang Zijie Yan Zhenyu Zhang School of Physics and Technology Wuhan University Wuhan 430072 China School of Materials Science and Engineering State Key Laboratory of New Ceramics and Fine Processing Tsinghua University Beijing 100084 China International Center for Quantum Design of Functional Materials (ICQD) Hefei Laboratory for Physical Sciences at Microscale (HFNL) and Synergetic Innovation Center of Notional Quantum Information and Quantum Physics University of Science and Technology of China Hefei 230026 China Department of Chemical and Biomolecular Engineering Clarkson University Potsdam New York 13699 USA

Contrasting room-temperature hydrogen sensing behaviors have been revealed for Pt-TiO2 and Pt-SnO2 composite nanoceramics. In the case of the Pt-TiO2 nanoceramics, the ultrahigh hydrogen sensitivities are lost abruptly when the oxygen/hydrogen concentration ratio in ambient atmosphere reaches a critical value. However, in the case of the Pt-SnO2 nanoceramics, such a phenomenon does not occur, and the extraordinary room-temperature hydrogen sensing capabilities are observed in the presence of oxygen in air. Our combined experimental and theoretical investigations establish a unified mechanism for both the systems, which is rooted in hydrogen chemisorption on the surface and interstitial lattice sites of SnO2 and TiO2; the difference in stability of the chemisorbed hydrogen on SnO2 and TiO2 is considered responsible for the contrasting hydrogen sensing capabilities. The central findings are helpful in enriching our microscopic understanding of hydrogen interaction with various metal oxide semiconductors （MOSs） at room temperature in varying mixed gaseous concentrations, and they could be instrumental in developing reliable room-temperature hydrogen sensors based on bulk MOSs.

关键词： Sn02 nanoceramics sensors hydrogen room-temperature

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