检索结果-内蒙古大学图书馆

SSRN 2024年

作者： Yu, Sung-Bo Susanto, Dieky Chang, Eun-Seo Shin, Hyeung-Keun Jeon, Young-Gyu Hwang, Sang-Yeop Kim, Hyun-Kyung Department of Battery Convergence Engineering Kangwon National University Chuncheon24341 Korea Republic of Interdisciplinary Program in Advanced Functional Materials and Devices Development Kangwon National University Chuncheon24341 Korea Republic of

Black phosphorus (BP) is a potential anode material for sodium-ion batteries due to its high theoretical capacity. However, large volume changes during electrochemical cycling prevent its practical application. Targeted covalent (P–O–C) bonding in a BP/reduced graphene oxide (rGO) composite was increased via high-energy mechanical milling. By attaching oxygen functional groups at the basal and edge planes, a BP/rGO composite with abundant P–O–C bonds was obtained, suppressing volume expansion during cycling. The total chemical bonding in the composite increased by 164%, enhancing the cycle retention from 6.3 to 60.9% over 100 cycles at 1 A g−1. © 2024, The Authors. All rights reserved.

关键词： Sodium-ion batteries

来源：评论

学校读者我要写书评

暂无评论

Coupled adsorption-photocatalysis process for the removal of diclofenac using magnetite/reduced graphene oxide nanocomposite

引用

Chemosphere 2024年 349卷 140788页

作者： Lee, Jooyoung Jo, Seong-Jun Yoon, Soyeong Ko, Mingi Jang, Taesoon Kim, Hyun-Kyung Park, Jeong-Ann Department of Environmental Engineering Kangwon National University Chuncheon24341 Korea Republic of Department of Battery Convergence Engineering Kangwon National University Chuncheon24341 Korea Republic of Interdisciplinary Program in Advanced Functional Materials and Devices Development Kangwon National University Chuncheon24341 Korea Republic of Department of Integrated Energy and Infra System Kangwon National University Chuncheon24341 Korea Republic of

Diclofenac (DCF) is frequently detected in water bodies (ng/L to g/L) as it is not completely removed by conventional wastewater treatment plants. Adsorption and photocatalysis have been studied as promising methods for treating DCF;however, both processes have limitations. Thus, in this study, the removal efficiency of DCF is evaluated using a magnetite/reduced graphene oxide (Fe3O4/RGO) nanocomposite via a coupled adsorption-catalysis process. The Fe3O4/RGO nanocomposite was successfully synthesized using a microwave-assisted solvothermal method and exhibited a bandgap of 2.60 eV. The kinetic data best fitted the Elovich model (R2 = 0.994, χ2 = 0.29), indicating rapid adsorption. The maximum DCF adsorption capacity calculated using the Langmuir model was 80.33 mg/g. An ultraviolet C (UVC) light source and 0.1 g/L of Fe3O4/RGO nanocomposite were the optimum conditions for the removal of DCF (C0 = 30 mM) by a coupled adsorption-photocatalysis process (first-order rate constant (k) = 0.088/min), which was greater than the single adsorption (k = 0.029/min) and pre-adsorption and post-photocatalysis (k = 0.053/min) processes. This indicates that the adsorbed DCF did not hamper the photocatalytic reaction of the Fe3O4/RGO nanocomposite, but rather enhanced the coupled adsorption-photocatalytic reaction. DCF removal efficiency was higher at acidic conditions (pH 4.3–5.0), because high H+ promotes the generation of certain reactive oxygen species (ROS) and increases of electrostatic interaction. The presence of NaCl and CaCl2 (10 mM) did not notably affect the total DCF removal efficiency;however, Ca2+ affected the initial DCF adsorption affinity. Scavenger experiments demonstrated O2∙− and h+ play a key ROS than ·OH to degrade DCF. The acute toxicity of DCF towards Aliivibrio fischeri gradually decreased with increasing treatment time. © 2023 Elsevier Ltd

关键词： Magnetite

来源：评论

学校读者我要写书评

暂无评论

Nano-Engineered Ga-Doped Llzo Electrolytes: A Leap Toward High-Performance Solid-State Batteries

SSRN

引用

SSRN 2023年

作者： Jo, Seong-Jun Jeon, Young-Gue Hwang, Sang-Yeop Lim, Sung-Hwan Kumar, Ramachandran Vasant Kim, Kwang-Bum Kim, Hyun-Kyung Department of Battery Convergence Engineering Kangwon National University 1 Kangwondaehak-gil Chuncheon24341 Korea Republic of Interdisciplinary Program in Advanced Functional Materials and Devices Development Kangwon National University Chuncheon24341 Korea Republic of Department of Materials Science and Metallurgy University of Cambridge 27 Charles Babbage Road CambridgeCB3 0FS United Kingdom Department of Materials Science and Engineering Yonsei University 134 Shinchon-dong Seodaemoon-gu Seoul120-749 Korea Republic of

Garnet-type Li7La3Zr2O12 (LLZO) Li-ion solid electrolytes are promising candidates for the next generation of safe solid-state batteries. However, the lack of a methodology to control the ceramic powder particle size for obtaining and densifying fast-ion-conducting cubic garnet hinders the application of the Li7La3Zr2O12 as a Li+ ion solid electrolyte. In this study, the doping concentration of Ga, calcination temperature of the Ga-doped LLZO (Ga-LLZO) precursor for achieving nanostructured powders, and the evolution of grain size during sintering conditions are explored to determine the optimum parameters to prepare highly conductive ceramics using the microwave-assisted solvothermal method. The nanostructured precursor (−3 S cm−1) that be employed as a solid electrolyte in a lithium-ion battery. The above approach opens up a new synthesis avenue for making doped Li7La3Zr2O12-type materials with improved properties for energy storage applications. © 2023, The Authors. All rights reserved.

关键词： Solid electrolytes

来源：评论

学校读者我要写书评

暂无评论

Recent progress on surface chemistryⅡ:Property and characterization

引用

Chinese Chemical Letters 2025年第1期36卷 8-57页

作者： Xin Li Zhen Xu Donglei Bu Jinming Cai Huamei Chen Qi Chen Ting Chen Fang Cheng Lifeng Chi Wenjie Dong Zhenchao Dong Shixuan Du Qitang Fan Xing Fan Qiang Fu Song Gao Jing Guo Weijun Guo Yang He Shimin Hou Ying Jiang Huihui Kong Baojun Li Dengyuan Li Jie Li Qing Li Ruoning Li Shuying Li Yuxuan Lin Mengxi Liu Peinian Liu Yanyan Liu Jingtao Lü Chuanxu Ma Haoyang Pan JinLiang Pan Minghu Pan Xiaohui Qiu Ziyong Shen Qiang Sun Shijing Tan Bing Wang Dong Wang Li Wang Lili Wang Tao Wang Xiang Wang Xingyue Wang Xueyan Wang Yansong Wang Yu Wang Kai Wu Wei Xu Na Xue Linghao Yan Fan Yang Zhiyong Yang Chi Zhang Xue Zhang Yang Zhang Yao Zhang Xiong Zhou Junfa Zhu Yajie Zhang Feixue Gao Yongfeng Wang Center for Carbon-based Electronics and Key Laboratory for the Physics and Chemistry of Nanodevices School of ElectronicsPeking UniversityBeijing 100871China Spin-X Institute School of MicroelectronicsSouth China University of TechnologyGuangzhou 511442China School of Materials and Energy Guangzhou Key Laboratory of Low-Dimensional Materials and Energy Storage DevicesGuangdong University of TechnologyGuangzhou 510006China Faculty of Materials Science and Engineering Kunming University of Science and TechnologyKunming 650093China i-Lab CAS Key Laboratory of Nanophotonic Materials and DevicesSuzhou Institute of Nano-Tech and Nano-BionicsChinese Academy of SciencesSuzhou 215123China CAS Key Laboratory of Molecular Nanostructure and Nanotechnology CAS Research/Education Center for Excellence in Molecular SciencesBeijing National Laboratory for Molecular Sciences(BNLMS)Institute of ChemistryChinese Academy of SciencesBeijing 100190China State Key Laboratory for Organic Electronics and Information Displays&Jiangsu Key Laboratory for Biosensors Institute of Advanced MaterialsJiangsu National Synergetic Innovation Center for Advanced MaterialsNanjing University of Posts and TelecommunicationsNanjing 210023China Institute of Functional Nano and Soft Materials(FUNSOM) Jiangsu Key Laboratory for Carbon-Based Functional Materials and DevicesSoochow UniversitySuzhou 215123China Hefei National Research Center for Physical Sciences at the Microscale and Synergetic Innovation Center of Quantum Information and Quantum Physics University of Science and Technology of ChinaHefei 230026China Institute of Physics&University of Chinese Academy of Sciences Beijing 100190China State Key Laboratory of Catalysis Dalian Institute of Chemical PhysicsChinese Academy of SciencesDalian 116023China College of Chemistry Beijing Normal UniversityBeijing 100875China Beijing National Laboratory for Molecular Sciences(BNLMS) College of Chemistry and Molecular EngineeringPeking UniversityBeijing 100871China School

Surface with well-defined components and structures possesses unique electronic,magnetic,optical and chemical *** a result,surface chemistry research plays a crucial role in various fields such as catalysis,energy,materials,quantum,and *** science mainly investigates the correspondence between surface property and *** probe microscopy(SPM)techniques are important tools to characterize surface properties because of the capability of atomic-scale imaging,spectroscopy and manipulation at the single-atom *** this review,we summarize recent advances in surface electronic,magnetic and optical properties characterized mainly by SPM-based *** focus on elucidating theπ-magnetism in graphene-based nanostructures,construction of spin qubits on surfaces,topology properties of surface organic structures,STM-based light emission,tip-enhanced Raman spectroscopy and integration of machine learning in SPM studies.

关键词： Surface chemistry Scanning probe microscopy π-Magnetism Spin qubits Tip-enhanced Raman spectroscopy

来源：评论

学校读者我要写书评

暂无评论

Recent progress on surface chemistryⅠ:Assembly and reaction

引用

Chinese Chemical Letters 2024年第12期35卷 43-94页

作者： Xin Li Zhen Xu Donglei Bu Jinming Cai Huamei Chen Qi Chen Ting Chen Fang Cheng Lifeng Chi Wenjie Dong Zhenchao Dong Shixuan Du Qitang Fan Xing Fan Qiang Fu Song Gao Jing Guo Weijun Guo Yang He Shimin Hou Ying Jiang Huihui Kong Baojun Li Dengyuan Li Jie Li Qing Li Ruoning Li Shuying Li Yuxuan Lin Mengxi Liu Peinian Liu Yanyan Liu Jingtao Lü Chuanxu Ma Haoyang Pan JinLiang Pan Minghu Pan Xiaohui Qiu Ziyong Shen Shijing Tan Bing Wang Dong Wang Li Wang Lili Wang Tao Wang Xiang Wang Xingyue Wang Xueyan Wang Yansong Wang Yu Wang Kai Wu Wei Xu Na Xue Linghao Yan Fan Yang Zhiyong Yang Chi Zhang Xue Zhang Yang Zhang Yao Zhang Xiong Zhou Junfa Zhu Yajie Zhang Feixue Gao Yongfeng Wang Center for Carbon-based Electronics and Key Laboratory for the Physics and Chemistry of Nanodevices School of ElectronicsPeking UniversityBeijing 100871China Spin-X Institute School of MicroelectronicsSouth China University of TechnologyGuangzhou 511442China School of Materials and Energy Guangzhou Key Laboratory of Low-Dimensional Materials and Energy Storage DevicesGuangdong University of TechnologyGuangzhou 510006China Faculty of Materials Science and Engineering Kunming University of Science and TechnologyKunming 650093 China i-Lab CAS Key Laboratory of Nanophotonic Materials and DevicesSuzhou Institute of Nano-Tech and Nano-BionicsChinese Academy of SciencesSuzhou 215123China CAS Key Laboratory of Molecular Nanostructure and Nanotechnology CAS Research/Education Center for Excellence in Molecular SciencesBeijing National Laboratory for Molecular Sciences(BNLMS)Institute of ChemistryChinese Academy of SciencesBeijing 100190China State Key Laboratory for Organic Electronics and Information Displays&Jiangsu Key Laboratory for Biosensors Institute of Advanced MaterialsJiangsu National Synergetic Innovation Center for Advanced MaterialsNanjing University of Posts and TelecommunicationsNanjing 210023China Institute of Functional Nano and Soft Materials(FUNSOM) Jiangsu Key Laboratory for Carbon-Based Functional Materials and DevicesSoochow UniversitySuzhou 215123China Hefei National Research Center for Physical Sciences at the Microscale and Synergetic Innovation Center of Quantum Information and Quantum Physics University of Science and Technology of ChinaHefei 230026China Institute of Physics&University of Chinese Academy of Sciences Beijing 100190China State Key Laboratory of Catalysis Dalian Institute of Chemical PhysicsChinese Academy of SciencesDalian 116023China College of Chemistry Beijing Normal UniversityBeijing 100875China Beijing National Laboratory for Molecular Sciences(BNLMS) College of Chemistry and Molecular EngineeringPeking UniversityBeijing 100871China School

Surface chemistry focuses on the investigation of the adsorption,migration,assembly,activation,reaction,and desorption of atoms and molecules at *** chemistry plays the pivotal roles in both fundamental science and applied *** review will summarize the recent progresses on surface assembly,synthesis and catalysis investigated mainly by scanning tunneling microscopy and atomic force *** assemblies of water and small biomolecules,construction of Sierpin′ski triangles and surface chirality are ***-surface synthesis of conjugated carbo-and heterocycles and other kinds of carbon nanostructures are *** model catalysis,including single-atom catalysis and electrochemical catalysis,are discussed at the single-atom level.

关键词： Surface chemistry Assembly Surface synthesis Catalysis on surface Surface electrochemical processes

来源：评论

学校读者我要写书评

暂无评论

Dual Chemifunctional Tin(Iv) Oxide/Nanoperforated Graphene Interlayer as a Polysulfide Adsorbent for Use in High-Performance Lithium-Sulfur Batteries

SSRN

引用

SSRN 2023年

作者： Lee, Junho Jung, Nae Yeon Ahn, Wook Lim, Hyung-Kyu Kim, Hyun-Kyung Department of Battery Convergence Engineering Kangwon National University 1 Kangwondaehak-gil Chuncheon24341 Korea Republic of Interdisciplinary Program in Advanced Functional Materials and Devices Development Kangwon National University Chuncheon24341 Korea Republic of Division of Chemical Engineering and Bioengineering Kangwon National University 1 Kangwondaehak-gil Chuncheon24341 Korea Republic of Department of Energy Engineering Soonchunhyang University 22 Soonchunhyang-ro Shinchang-myeon Chungcheongnam-do Asan-Si31538 Korea Republic of

The development of Li-S batteries is limited by their levels of rapid capacity decay owing to polysulfide dissolution and diffusion in organic electrolytes. We addressed this critical issue by fabricating a dual chemifunctional interlayer comprising SnO2 nanoparticles and nanoperforated graphene (NPG) that could function as a polysulfide adsorbent. The synergistic effects of SnO2 and the high-density functional groups of NPG on polysulfide capture were conceptually confirmed. NPG not only supported the adsorption of Li polysulfides but also provided pathways for simple Li-ion motion within the SnO2/NPG interlayer. A cell assembled with the SnO2/NPG interlayer displayed a high rate capability and initial discharge capacity and good reversible capacity. The excellent high-rate cycling performance of the cathode could mainly be attributed to the strong chemical bonds formed between SnO2/NPG and the polysulfides, rapid electron transfer, and optimized ion diffusion pathways derived from the well-organized structure of the composite. Synthesizing dual chemifunctional interlayers using a composite of metal oxides and NPG may lead to the development of advanced Li-S batteries with numerous practical applications in the near future. © 2023, The Authors. All rights reserved.

关键词： Lithium sulfur batteries

来源：评论

学校读者我要写书评

暂无评论

An in-situ defect passivation through a green anti-solvent approach for high-efficiency and stable perovskite solar cells

引用

Science Bulletin 2021年第14期66卷 1419-1428,M0004页

作者： Chang Liu Lei Huang Xianyong Zhou Xingzhu Wang Jianxi Yao Zhike Liu Shengzhong Frank Liu Wanli Ma Baomin Xu Academy for Advanced Interdisciplinary Studies Southern University of Science and TechnologyShenzhen 518055China Department of Materials Science and Engineering and Shenzhen Engineering Research and Development Center for Flexible Solar Cells Southern University of Science and TechnologyShenzhen 518055China Key Laboratory of Energy Conversion and Storage Technologies(Southern University of Science and Technology) Ministry of EducationShenzhen 518055China Guangdong-Hong Kong-Macao Joint Laboratory for Photonic-Thermal-Electrical Energy Materials and Devices Southern University of Science and TechnologyShenzhen 518055China State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources North China Electric Power UniversityBeijing 102206China Key Laboratory of Applied Surface and Colloid Chemistry(Ministry of Education) Shaanxi Key Laboratory for Advanced Energy DevicesShaanxi Engineering Laborartory for Advanced Energy TechnologySchool of Materials Science and EngineeringShaanxi Normal UniversityXi’an 710119China Institute of Functional Nano&Soft Materials Jiangsu Key Laboratory for Carbon-Based Functional Materials&DevicesJoint International Research Laboratory of Carbon-Based Functional Materials and DevicesSoochow UniversitySuzhou 215123China

Surface and grain boundary defects in halide perovskite solar cells are highly detrimental,reducing efficiencies and *** halide anion and organic cation defects usually aggravate ion diffusion and material degradation on the surfaces and at the grain boundaries of perovskite *** this study,we employ an in-situ green method utilizing nontoxic cetyltrimethylammonium chloride(CTAC)and isopropanol(IPA)as anti-solvents to effectively passivate both surface and grain boundary defects in hybrid *** vacancies can be readily passivated by the chloride group due to its high electronegativity,and cation defects can be synchronously passivated by the more stable cetyltrimethylammonium *** results show that the charge trap density was significantly reduced,while the carrier recombination lifetime was markedly *** a result,the power conversion efficiency of the cell can reach 23.4%with this in-situ green *** addition,the device retains 85%of its original power conversion efficiency after 600 h of operation under illumination,showing that the stability of perovskite solar cells is improved with this in-situ passivation *** work may provide a green and effective route to improve both the stability and efficiency of perovskite solar cells.

关键词： Perovskite solar cells In-situ defect passivation Green anti-solvent

来源：评论

学校读者我要写书评

暂无评论

Disorder-driven glasslike thermal conductivity in colusite Cu26V2Sn6S32 investigated by Mössbauer spectroscopy and inelastic neutron scattering

引用

Physical Review materials 2020年第2期4卷 025404-025404页

作者： Christophe Candolfi Gabin Guélou Cédric Bourgès Andrew R. Supka Rabih Al Rahal Al Orabi Marco Fornari Bernard Malaman Gérard Le Caër Pierric Lemoine Vincent Hardy Jean-Marc Zanotti Raju Chetty Michihiro Ohta Koichiro Suekuni Emmanuel Guilmeau Institut Jean Lamour UMR 7198 CNRS – Université de Lorraine 2 allée André Guinier-Campus ARTEM BP 50840 54011 Nancy Cedex France Laboratoire CRISMAT UMR 6508 CNRS ENSICAEN 6 Boulevard du Maréchal Juin 14050 Caen Cedex 04 France Department of Physics and Science of Advanced Materials Program Central Michigan University Mt. Pleasant Michigan 48859 United States Solvay Design and Development of Functional Materials Department AXEL’ ONE Collaborative Platform − Innovative Materials 87 Rue des Freres Perret − BP62 69192 Saint Fons Cedex France Institut de Physique de Rennes UMR UR1-CNRS 6251 Université de Rennes I Campus de Beaulieu 35042 Rennes Cedex France Université de Rennes CNRS ISCR – UMR 6226 F-35000 Rennes France Laboratoire Léon Brillouin CNRS-CEA (UMR 12) CNRS Université Paris-Saclay CEA Saclay 91191 Gif-sur-Yvette Cedex France Research Institute for Energy Conservation National Institute of Advanced Industrial Science and Technology (AIST) Tsukuba Ibaraki 305–8568 Japan Department of Applied Science for Electronics and Materials Interdisciplinary Graduate School of Engineering Sciences Kyushu University Kasuga Fukuoka 816–8580 Japan

The influence of structural disorder on the thermal transport in the colusite Cu26V2Sn6S32 has been investigated by means of low-temperature thermal conductivity and specific heat measurements (2–300 K), Sn119 Mössbauer spectroscopy and temperature-dependent powder inelastic neutron scattering (INS). Variations in the high-temperature synthesis conditions act as a key parameter for tuning the degree of disorder in colusite compounds. Intriguingly, we find that all synthesized samples are disordered, the degree of which varies with the synthesis conditions used. Mössbauer data clearly evidence that Sn atoms do not solely occupy the 6c site of the crystal lattice but are present on possibly both the Cu and V sites, leading to a random distribution of these three cations within the unit cell. Increasing the disorder in these materials tends to lead to a smearing out of the main features in the phonon density of states measured by INS. Although the evolution of the inelastic signal upon warming is well described by a quasiharmonic approximation, elastic properties calculations indicate large average Grüneisen parameters, consistent with those determined experimentally from thermodynamic data. Increasing the level of disorder results in a decreased average Grüneisen parameter suggesting that the lowered lattice thermal conductivity is not driven by enhanced anharmonicity. These results provide experimental evidence to support that the remarkable changeover in the lattice thermal conductivity from crystalline to glasslike is solely driven by enhanced disorder accompanied by local lattice distortions.

关键词： Thermal properties Polycrystalline materials Mössbauer spectroscopy Time-of-flight neutron spectroscopy

来源：评论

学校读者我要写书评

暂无评论

Copper-Rich Thermoelectric Sulfides: Size-Mismatch Effect and Chemical Disorder in the [TS4]Cu6 Complexes of Cu26T2Ge6S32 (T=Cr, Mo, W) Colusites

引用

advanced materials 2019年第43期58卷 15601-15609页

作者： Kumar, Ventrapati Pavan Guélou, Gabin Lemoine, Pierric Raveau, Bernard Supka, Andrew R. Orabi, Rabih Al Rahal Al Fornari, Marco Suekuni, Koichiro Guilmeau, Emmanuel CRISMAT CNRS Normandie Univ ENSICAEN UNICAEN Caen14000 France Univ Rennes CNRS ISCR – UMR 6226 Rennes35000 France Department of Physics and Science of Advanced Materials Program Central Michigan University Mt. PleasantMI48859 United States Department of Applied Science for Electronics and Materials Interdisciplinary Graduate School of Engineering Sciences Kyushu University Kasuga Fukuoka816-8580 Japan Solvay Design and Development of Functional Materials Department Axel’One 87 avenue des Frères Perret Saint Fons Cedex69192 France

Herein, we investigate the Mo andWsubstitution for Cr in synthetic colusite, Cu26Cr2Ge6S32. Primarily, we elucidate the origin of extremely low electrical resistivity which does not compromise the Seebeck coefficient and leads to outstanding power factors of 1.94 mWm−1K−2 at 700 K in Cu26Cr2Ge6S32. We demonstrate that the abnormally long iono-covalent T–S bonds competing with short metallic Cu–T interactions govern the electronic transport properties of the conductive „Cu26S32" framework. We address the key role of the cationic size-mismatch at the core of the mixed tetrahedral–octahedral complex over the transport properties. Two essential effects are identified: 1) only the tetrahedra that are directly bonded to the [TS4]Cu6 complex are significantly distorted upon substitution and 2) the major contribution to the disorder is localized at the central position of the mixed tetrahedral–octahedral complex, and is maximized for x=1, i.e. for the highest cationic sizevariance, σ2. © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

关键词： Copper compounds

来源：评论

学校读者我要写书评

暂无评论

Native diversity buffers against severity of non-native tree invasions ( vol 621,pg 773 , 2023 )

引用

NATURE 2023年第7982期622卷 E2-E2页

作者： Delavaux, Camille S. Crowther, Thomas W. Zohner, Constantin M. Robmann, Niamh M. Lauber, Thomas van den Hoogen, Johan Kuebbing, Sara Liang, Jingjing de-Miguel, Sergio Nabuurs, Gert-Jan Reich, Peter B. Abegg, Meinrad Yao, Yves C. Adou Alberti, Giorgio Zambrano, Angelica M. Almeyda Alvarado, Braulio Vilchez Alvarez-Davila, Esteban Alvarez-Loayza, Patricia Alves, Luciana F. Ammer, Christian Anton-Fernandez, Clara Araujo-Murakami, Alejandro Arroyo, Luzmila Avitabile, Valerio Aymard, Gerardo A. Baker, Timothy R. Balazy, Radomir Banki, Olaf Barroso, Jorcely G. Bastian, Meredith L. Bastin, Jean-Francois Birigazzi, Luca Birnbaum, Philippe Bitariho, Robert Boeckx, Pascal Bongers, Frans Bouriaud, Olivier Brancalion, Pedro H. S. Brandl, Susanne Brienen, Roel Broadbent, Eben N. Bruelheide, Helge Bussotti, Filippo Gatti, Roberto Cazzolla Cesar, Ricardo G. Cesljar, Goran Chazdon, Robin Chen, Han Y. H. Chisholm, Chelsea Cho, Hyunkook Cienciala, Emil Clark, Connie Clark, David Colletta, Gabriel D. Coomes, David A. Valverde, Fernando Cornejo Corral-Rivas, Jose J. Crim, Philip M. Cumming, Jonathan R. Dayanandan, Selvadurai de Gasper, Andre L. Decuyper, Mathieu Derroire, Geraldine DeVries, Ben Djordjevic, Ilija Dolezal, Jiri Dourdain, Aurelie Obiang, Nestor Laurier Engone Enquist, Brian J. Eyre, Teresa J. Fandohan, Adande Belarmain Fayle, Tom M. Feldpausch, Ted R. Ferreira, Leandro V. Fischer, Markus Fletcher, Christine Frizzera, Lorenzo Gamarra, Javier G. P. Gianelle, Damiano Glick, Henry B. Harris, David J. Hector, Andrew Hemp, Andreas Hengeveld, Geerten Herault, Bruno Herbohn, John L. Herold, Martin Hillers, Annika Coronado, Euridice N. Honorio Hui, Cang Ibanez, Thomas T. Amaral, Ieda Imai, Nobuo Jagodzinski, Andrzej M. Jaroszewicz, Bogdan Johannsen, Vivian Kvist Joly, Carlos A. Jucker, Tommaso Jung, Ilbin Karminov, Viktor Kartawinata, Kuswata Kearsley, Elizabeth Kenfack, David Kennard, Deborah K. Kepfer-Rojas, Sebastian Keppel, Gunnar Khan, Mohammed Latif Killeen, Timothy J. Kim, Hyun Seok Kitayama, Kanehiro Kohl, Michael Korju Institute of Integrative Biology ETH Zurich (Swiss Federal Institute of Technology) Zurich Switzerland Department of Genetics Evolution and Environment University College London London UK The Forest School at The Yale School of the Environment Yale University New Haven CT USA Department of Forestry and Natural Resources Purdue University West Lafayette IN USA Department of Agriculture Forestry and Bioresources Seoul National University Seoul South Korea Department of Crop and Forest Sciences University of Lleida Lleida Spain Joint Research Unit CTFC–AGROTECNIO–CERCA Solsona Spain Wageningen University and Research Wageningen The Netherlands World Agroforestry (ICRAF) Nairobi Kenya Department of Forest Resources University of Minnesota St Paul MN USA Hawkesbury Institute for the Environment Western Sydney University Penrith New South Wales Australia Institute for Global Change Biology and School for Environment and Sustainability University of Michigan Ann Arbor MI USA Swiss Federal Institute for Forest Snow and Landscape Research WSL Birmensdorf Switzerland UFR Biosciences University Félix Houphouët-Boigny Abidjan Côte d’Ivoire Department of Agricultural Food Environmental and Animal Sciences University of Udine Udine Italy Faculty of Science and Technology Free University of Bolzano Bolzano Italy Spatial Ecology and Conservation Laboratory Department of Tourism Recreation and Sport Management University of Florida Gainesville FL USA Forestry School Tecnológico de Costa Rica TEC Cartago Costa Rica Fundacion ConVida Universidad Nacional Abierta y a Distancia UNAD Medellin Colombia Field Museum of Natural Histiory Chicago IL USA Center for Tropical Research Institute of the Environment and Sustainability UCLA Los Angeles CA USA Silviculture and Forest Ecology of the Temperate Zones University of Göttingen Göttingen Germany Division of Forest and Forest Resources Norwegian Institute of Bioeconomy Research (NIBIO) Ås Norway Museo de Hi

来源：评论

学校读者我要写书评

暂无评论

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

请选择保存的检索档案：

请选择收藏分类：

通借通还

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：