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中国有色金属学会会刊：英文版 2009年第4期19卷 1018-1022页

作者： Jae-Hyun NOH Kwan-Yo ung lee joong-kee lee Battery Research Center Korea Institute of Science and Technology Department of Chemical and Biological Engineering Korea University

Phosphorus doped silicon-carbon composite particles were synthesized through a DC arc plasma ***(SiH4) and methane(CH4) were introduced into the reaction chamber as the precursor of silicon and carbon,***(PH3) was used as a phosphorus dopant *** of synthesized particles were carried out by scanning electron microscopy(SEM),X-ray diffractometry(XRD),X-ray photoelectron spectroscopy(XPS) and bulk resistivity *** properties were investigated by cyclic test and electrochemical voltage spectroscopy(EVS).In the experimental range,phosphorus doped silicon-carbon composite electrode exhibits enhanced cycle performance than intrinsic silicon and phosphorus doped *** can be explained that incorporation of carbon into silicon acts as a buffer matrix and phosphorus doping plays an important role to enhance the conductivity of the electrode,which leads to the improvement of the cycle performance of the cell.

关键词：电化学特性磷掺杂负极活性材料磷硅电池材料锂离子 X射线光电子能谱扫描电子显微镜

Employment of encapsulated Si with mesoporous TiO_2 layer as anode material for lithium secondary batteries

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中国有色金属学会会刊：英文版 2009年第4期19卷 1023-1026页

作者： Sang-Eun PARK Bo-Eun KIM Sang-Wha lee joong-kee lee Advanced Energy Materials Processing Laboratory Korea Institute of Science and Technology Department of Chemical & Bio Engineering Kyungwon University

Silicon composite of nano-capsule type is newly applied as an active anode material for lithium ion ***2-encapsulated silicon powders were synthesized by a sol-gel reaction with titanium *** nanoparticles were successfully embedded into porous titanium oxide capsules that played as a buffer layer against drastic volume changes of silicon during the charge-discharge cycling,consequently leading to the retardation of the capacity fading of intrinsic silicon *** electrochemical and structural properties of silicon nanocomposites with different surface areas of encapsulating TiO2 layer were characterized by X-ray diffraction(XRD),nitrogen gas adsorption analysis by the Brunauer-Emmett-Teller(BET) equation,transmission electron microscopy(TEM),and galvanostatic charge-discharge experiments.

关键词：二氧化钛硅材料锂二次电池负极材料封装纳米复合材料透射电子显微镜就业

Stable Zn Metal Anodes with Limited Zn-Doping in MgF_(2) Interphase for Fast and Uniformly Ionic Flux

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Nano-Micro Letters 2022年第3期14卷 169-183页

作者： Ji Young Kim Guicheng Liu Ryanda Enggar Anugrah Ardhi Jihun Park Hansung Kim joong kee lee Energy Storage Research Center Korea Institute of Science and TechnologyHwarang‑ro 14‑gil 5Seongbuk‑guSeoul 02792Republic of Korea Department of Chemical and Biomolecular Engineering Yonsei University50 Yonsei‑roSeodaemun‑guSeoul 03722Republic of Korea Department of Physics Dongguk UniversitySeoul 04620Republic of Korea APC Technology 10868 Gangbyeonyeok‑ro‑4‑gilGwangjin‑guSeoul 05116Republic of Korea Department of Energy and Environmental Engineering KIST SchoolKorea University of Science and TechnologyHwarang‑ro 14‑gil 5Seongbuk‑guSeoul 02792Republic of Korea

The practical applications of aqueous Zn metal batteries are currently restricted by the inherent drawbacks of Zn such as the hydrogen evolution reaction,sluggish kinetics,and dendrite *** address these problems,herein,a limitedly Zn-doped MgF_(2)interphase comprising an upper region of pure,porous MgF_(2)and a lower region of gradient Zn-doped MgF_(2)is achieved via radio frequency sputtering *** porous MgF_(2)region is a polar insulator whose high corrosion resistance facilitates the de-solvation of the solvated Zn ions and suppression of hydrogen evolution,resulting in Zn metal electrodes with a low interfacial *** Zn-doped MgF_(2)region facilitates fast transfer kinetics and homogeneous deposition of Zn ions owing to the interfacial polarization between the Zn dopant and MgF_(2)matrix,and the high concentration of the Zn dopant on the surface of the metal substrate as fine ***,a symmetric cell incorporating the proposed Zn metal exhibits low overpotentials of~27.2 and~99.7 mV without Zn dendrites over 250 to 8000 cycles at current densities of 1.0 and 10.0 mA cm−2,*** developed Zn/MnO2 full cell exhibits superior capacity retentions of 97.5%and 84.0%with average Coulombic efficiencies of 99.96%after 1000 and 3000 cycles,respectively.

关键词： Zinc metal battery MgF_(2)layer Limited zinc doping Ion-transfer kinetic Deposition guidance

Effect of metal catalyst on the mechanism of hydrogen spillover in three-dimensional covalent-organic frameworks

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Chinese Physics B 2017年第2期26卷 412-419页

作者： Xiu-Ying Liu Jing-Xin Yu Xiao-Dong Li Gui-Cheng Liu Xiao-Feng Li joong-kee lee College of Science Henan University of Technology Zhengzhou 450000 China Center for Energy Convergence Research Green City Research Institute Korea Institute of Science and Technology (KIST) Seou102792 Republic of Korea College of Physical and Electronic Information Luoyang Normal University Luoyang 471022 China

Hydrogen spillover mechanism of metal-supported covalent-organic frameworks COF-105 is investigated by means of the density functional theory, and the effects of metal catalysts M_4（Pt_4, Pd_4, and Ni_4） on the whole spillover process are systematically analyzed. These three metal catalysts exhibit several similar phenomena：（i） they prefer to deposit on the tetra（_4-dihydroxyborylphenyl） silane（TBPS） cluster with surface-contacted configuration;（ii） only the H atoms at the bridge site can migrate to 2,3,6,7,10,11-hexahydroxy triphenylene（HHTP） and TBPS surfaces, and the migration process is an endothermic reaction and not stable;（iii） the introduction of M_4 catalyst can greatly reduce the diffusion energy barrier of H atoms, which makes it easier for the H atoms to diffuse on the substrate surface. Differently, all of the H2 molecules spontaneously dissociate into H atoms onto Pt_4 and Pd_4clusters. However, the adsorbed H2 molecules on Ni_4 cluster show two types of adsorption states： one activated state with stretched H–H bond length of 0.88 ？A via the Kubas interaction and five dissociated states with separated hydrogen atoms. Among all the M_4 catalysts, the orders of the binding energy of M_4 deposited on the substrate and average chemisorption energy per H2 molecule are Pt_4〉Ni_4〉Pd_4. On the contrary, the orders of the migration and diffusion barriers of H atoms are Pt_4

关键词： covalent-organic frameworks hydrogen spillover hydrogen storage density functional theory

Reversible Zn/polymer heterogeneous anode

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Carbon Energy 2023年第6期5卷 82-91页

作者： Lingyun Xiong Hao Fu Kai Yang Ji Young Kim Ren Ren joong kee lee Woochul Yang Guicheng Liu Department of Physics Dongguk UniversitySeoulRepublic of Korea School of Energy Power and Mechanical Engineering North China Electric Power UniversityBeijingChina Energy Storage Research Center Clean Energy InstituteKorea Institute of Science and Technology(KIST)Seongbuk‐guSeoulRepublic of Korea Department of Materials Science and Engineering City University of Hong KongKowloonHong KongChina

Commercialization of Zn-metal anodes with low cost and high theoretical capacity is hindered by the poor reversibility caused by dendrites growth,side reactions,and the slow Zn^(2+)-transport and reaction ***,a reversible heterogeneous electrode of Zn-nanocrystallites/polyvinylphosphonic acrylamide(Zn/PPAm)with fast electrochemical kinetics is designed for the first time:phosphonic acid groups with strong polarity and chelation effect ensure structural reversibility and stability of the threedimensional Zn-storage-host PPAm network and the Zn/PPAm hybrid;hydrophobic carbon chains suppress side reactions such as hydrogen evolution and corrosion;weak electron-donating amide groups constitute Zn^(2+)-transport channels and promote“desolvation”and“solvation”effects of Zn^(2+)by dragging the PPAm network on the Zn-metal surface to compress/stretch during Zn plating/stripping,respectively;and the heterostructure and Zn nanocrystallites suppress dendrite growth and enhance electrochemical reactivity,***,the Zn/PPAm electrode shows cycle reversibility of over 6000 h with a hysteresis voltage as low as 31 mV in symmetrical cells and excellent durability and flexibility in fiber-shaped batteries.

关键词： dendrite-free electrode process kinetics fiber-shaped battery reversible metal/polymer heterostructure Zn-metal anode

Uniform Metal Sulfide@N-doped Carbon Nanospheres for Sodium Storage: Universal Synthesis Strategy and Superior Performance

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Energy & Environmental Materials 2023年第2期6卷 389-396页

作者： Kai Yang Hao Fu Yixue Duan Manxiang Wang Minh Xuan Tran joong kee lee Woochul Yang Guicheng Liu Department of Physics Dongguk UniversitySeoul 04620Korea Shaanxi Key Laboratory of Chemical Additives for Industry Shaanxi University of Science and TechnologyXi’an 710021China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China College of Physics and Electronic Information Yan’an UniversityYan’an 716000China Center for Energy Storage Research Clean Energy InstituteKorea Institute of Science and Technology(KIST)Seoul 02792Korea

Nitrogen-doped carbon-coated transition-metal sulfides(TMS@NCs)have been considered as efficient anodes for sodium-ion ***,the uncontrollable morphology and weak core-shell binding forces significantly limit the sodium storage performance and ***,based on the reversible ring-opening reaction of the epoxy group of the tertiary amino group-rich epoxide cationic polyacrylamide(ECP)at the beginning of hydrothermal process(acidic environment)and the irreversible ring-opening(cross-linking reactions)at the late hydrothermal period(alkaline environment),47 nm-sized ZnS@NCs were prepared via a one-pot hydrothermal *** this process,the covalent bonds formed between the ZnS core and elastic carbon shell significantly improved the mechanical and chemical stabilities of ZnS@*** from the nanosize,fast ion/electron transfer,and high stability,ZnS@NC exhibited a high reversible capacity of 421.9 mAh g^(−1) at a current density of 0.1 A g^(−1) after 1000 cycles and a superior rate capability of 273.8 mAh g^(−1) at a current density of 5 A g^(−1).Moreover,via this universal synthesis strategy,a series of TMS@NCs,such as MoS_(2)@NC,NiS@NC,and CuS@NC were developed with excellent capacity and cyclability.

关键词： anode materials core-shell structure nitrogen-doped carbon ring-opening reaction transition-metal sulfide

Ordered SnO nanoparticles in MWCNT as a functional host material for high-rate lithium-sulfur battery cathode

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Nano Research 2017年第6期10卷 2083-2095页

作者： A-Young Kim Min Kyu Kim Ji Young Kim Yuren Wen Lin Gu Van-Duong Dao Ho-Suk Choi Dongjin Byun joong kee lee Center for Energy Convergence Korea Institute of Science and Technology Seoul02792 Republic of Korea Department of Material Science and Engineering Korea University Seoul 02841 Republic of Korea Beijing National Laboratory for Condensed Matter Physics Institute of Physics Chinese Academy of Sciences Beijing 100190 China Department of Chemical Engineering & Applied Chemistry Chungnam National University Daejeon 34134 Republic of Korea

Lithium-sulfur battery has become one of the most promising candidates for next generation batteries, and it is still restricted due to the low sulfur conductivity, large volume expansion and severe polysulfide shuttling. Herein, we present a novel hybrid electrode with a ternary nanomaterial based on sulfur-impregnated multiwalled carbon nanotubes filled with ordered tin-monoxide nanoparticles （MWCNT-SnO/S）. Using a dry plasma reduction method, a mechanically robust material is prepared as a cathode host material for lithium-sulfur batteries. The MWCNT-SnO/S electrode exhibits high conductivity, good ability to capture polysulfides, and small volume change during a repeated charge-discharge process. In situ transmission electron microscopy and ultraviolet-visible absorption results indicate that the MWCNT-SnO host efficiently suppresses volume expansion during lithiation and reduces polysulfide dissolution into the electrolyte. Furthermore, the ordered SnO nanoparticles in the MWCNTs facilitate fast ion/electron transfer during the redox reactions by acting as connective links between the walls of the MWCNTs. The MWCNT-SnO/S cathode with a high sulfur content of 70 wt.% exhibits an initial discharge capacity of 1,682.4 mAh·g^-1 at 167.5 m·g^-1 （0.1 C rate） and retains a capacity of 530.1 mAh·g^-1 at 0.5 C after 1,000 cycles with nearly 100% Coulombic efficiency. Furthermore, the electrode exhibits the high capacity even at a high current rate of 20 C.

关键词： hybrid nanomaterial multiwalled carbonnanotube (MWCNT) ordered tin monoxide cathode high loading lithium-sulfur battery

Constructing“π–π”Reinforced Bridge Carbon Nanofibers with Highly Active Co‑N/C@pyridine N/C@CNTs Sites as Free‑Standing Bifunctional Oxygen Electrodes for Zn–Air Batteries

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Advanced Fiber Materials 2024年第4期6卷 1108-1121页

作者： Tuo Lu Nengneng Xu Liyuan Guo Benji Zhou Lingyu Dai Woochul Yang Guicheng Liu joong kee lee Jinli Qiao State Key Laboratory for Modification of Chemical Fibers and Polymer Materials and College of Environmental Science and Engineering Donghua UniversityShanghai 201620People’s Republic of China Shanghai Institute of Pollution Control and Ecological Security Shanghai 200092People’s Republic of China Department of Physics Dongguk UniversitySeoul 04620Republic of Korea School of Energy Power and Mechanical Engineering North China Electric Power UniversityBeijing 102206People’s Republic of China Energy Storage Research Center and Clean Energy Institute Korea Institute of Science and TechnologySeoul 02792Republic of Korea

Rechargeable Zn-air batteries(ZABs)have received extensive attention,while their real applications are highly restricted by the slow kinetics of the oxygen reduction and oxygen evolution reactions(ORR/OER).Herein,we report a“bridge”structured flexible self-supporting bifunctional oxygen electrode(CNT@Co-CNFF50-900)with strong active and stable Co-N/C@pyridine N/C@CNTs reaction *** from the electron distribution optimization and the advantages of hierarchical catalytic design,the CNT@Co-CNF_(F50-900)electrode had superior ORR/OER activity with a small potential gap(ΔE)of 0.74 *** by highly graphitized carbon and the“π-π”bond,the free-standing CNT@Co-CNFF50-900 electrode exhibited outstanding catalytic stability with only 36 mV ***,the CNT@Co-CNFF50-900-based liquid ZAB showed a high power density of 371 mW cm^(−2),a high energy density of 894 Wh kg^(−1),and a long cycling life of over 130 *** assembled quasi-solid-state ZAB also demonstrated a high power density,attaining 81 mW cm^(−2),with excellent charge-discharge durability beyond 100 h and extremely high flexibility under the multi-angle *** study provides an effective electrospinning solution for integrating high-efficiency electrocatalysts and electrodes for energy storage and conversion devices.

关键词： Electrospinning MOF-derived carbon tube Bifunctional oxygen catalytic electrode “Bridge”structure Zn–air battery

Correction to:Stable Zn Metal Anodes with Limited Zn-Doping in MgF2 Interphase for Fast and Uniformly Ionic Flux

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Nano-Micro Letters 2022年第4期14卷 289-289页

In the original version of the article affiliation 1 has been missed out for an author and affiliation 1 superscript has been added in this *** Original article has been *** kee lee1,5Open Access This article is licensed under a Creative Commons Attribution 4.0 International License,which permits use,sharing,adaptation,distribution and reproduction in any medium or format,as long as you give appropriate credit to the original author(s)and the source,provide a link to the Creative Commons licence,and indicate if changes were made.

关键词： Creative Open app

Comparative Optical Separation of Racemic Ibuprofen by Using Chiral Stationary Phase

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Chinese Journal of Chemical Engineering 2002年第6期10卷 681-685页

作者： Dalkeun PARK joong kee lee 等 Nano-EcoResearchCenter KISTSeoul136-791Korea ChemicalEngineeringDepartment HongikUniversitySeoul121-791Korea

Ibuprofen is widely used as a non-steroidal anti-inflammatory drug and produced as racemic mixture. Its pharmacological activity resides only in S-(+)-enantiomer, and R-()-enantiomer is not only inactive but also has many side effects. Thus it is necessary to separate R-enantiomer from racemic ibuprofen. We studied optical separation of racemic Ibuprofen with chiral high performance liquid chromatography (HPLC). Out of three different chiral stationary phases, which were selected on the basis of structure and availability, two were found to be ef-fective. There was optimum eluent composition for each stationary phase for good resolution in optical separation. Resolution decreased with increase of eluent flow rate, but effect of injection volume on resolution was insignificant at high eluent flow rate.

关键词： ibuprofen enantiomer separation high performance liquid chromatography chiral stationary phase