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Yifei Cai,Bin Qin,Chun Li,Xiaoqing Si,Jian Cao,Xiaohang Zheng,LIANG QIAO,Junlei Qi 한국공업화학회 2023 Journal of Industrial and Engineering Chemistry Vol.120 No.-
Lithium (Li) metal is a promising material for high-energy–density batteries, but it is still plagued byobvious capacity degradation and low average Coulombic efficiency resulting from dendrite Li propagation. One main reason is the electro-mechanic coupled failure of plated Li on the current collector, whichcontributes to non-dense Li deposition on the anode. Transition metal oxides (TMOs) with a conversiontypemechanism have been used directly as the anode materials for lithium ion batteries, which demonstratedbetter electro-mechanical stability than metal Li. Herein, a successive ’’conversion-deposition’’mechanism is ingeniously developed to restrain the generation of dendritic Li. Specifically, a microcrystallineCu2O modified current collector was prepared, in which Li+ are sequentially inserted intoCu2O and deposited in the form of Li metal at successive low potential. A Li-Cu half-cell based on thehybrid mechanism sustains a high Coulombic efficiency of over 99.3 % in up to 800 cycles. This work ingeniouslyinhibits the generation of dendrite Li by incorporating conversion-type materials withdeposition-dissolution type metal Li, which contributes to a novel concept for the design of functionalcurrent collectors for composite Li anodes.
Non-volatile, Li-doped ion gel electrolytes for flexible WO<sub>3</sub>-based electrochromic devices
Yun, Tae Yong,Li, Xinlin,Bae, Jaehyun,Kim, Se Hyun,Moon, Hong Chul Elsevier 2019 Materials & Design Vol.162 No.-
<P><B>Abstract</B></P> <P>Flexible electrochromic devices (ECDs) based on Li-doped ion gels and tungsten trioxide (WO<SUB>3</SUB>) are demonstrated. Colored ECDs cannot be produced using conventional ion gels comprised of copolymers and room temperature ionic liquids (RTILs) due to a lack of cations that can be inserted into WO<SUB>3</SUB>. Based on considerations of the coloration mechanism, we developed Li-doped ion gels and applied these to devices. The effects of Li salt concentration are systematically examined, with respect to device dynamics, coloration efficiency, and transmittance contrast. In addition, the coloration/bleaching switching stability of the ECD produced using optimal Li salt content is investigated. The ECD exhibits distinct colored and bleached states even after 24 h operation in air. Using the described Li-doped ion gel electrolytes, flexible WO<SUB>3</SUB> ECDs were successfully demonstrated with good bending stability and no electrolyte leakage.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Non-volatile, Li-doped ion gel electrolytes are designed for flexible WO<SUB>3</SUB>-based ECDs. </LI> <LI> ECDs exhibit low voltage operation (–0.9 V) and large transmittance contrast (~85%) between colored and bleached states. </LI> <LI> Electrolyte leakage is not observed in flexible ECDs containing Li-doped gel electrolyte when bending deformation is applied. </LI> <LI> Flexible ECDs maintain ~90.3 and ~84.5% of initial optical transmittance and coloration efficiency after 1000 bending tests. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>
Li, Yuanyuan,Mi, Yiming,Chung, Jin Suk,Kang, Sung Gu Elsevier 2018 International journal of hydrogen energy Vol.43 No.4
<P><B>Abstract</B></P> <P>The structural stability and hydrogen release properties of M-doped KMgH<SUB>3</SUB> (M = Li, Na, Rb, or Cs) were examined using density functional theory (DFT) calculations. The reaction enthalpies (ΔH) of the four possible dehydrogenation reaction pathways were calculated using the doped structures with different phases ( P m 3 ¯ m , P<I>nma</I>, and R3<I>c</I>). The most favorable reaction pathway among these four pathways was found. Among the dopants investigated, the most promising dopant for this reaction was Li. In addition, the application of pressure was found to be useful for tuning the reaction enthalpies of the dehydrogenation reactions. Overall, the results present an efficient means of designing new promising perovskite-type hydrides for hydrogen storage.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Perovskite-type KMgH<SUB>3</SUB> is a promising candidate for hydrogen storage. </LI> <LI> The most favorable reaction pathway of dehydrogenation reactions was examined. </LI> <LI> Li was the most useful and effective dopant to release hydrogen. </LI> <LI> Pressure can be usefully employed for tuning the reaction enthalpies of dehydrogenation reactions. </LI> </UL> </P>
Aijia Wei,Wen Li,Lihui Zhang,Xiaohui Li,Xue Bai,Zhenfa Liu 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2017 NANO Vol.12 No.5
Zn2+ and F- ions are successfully used to modify pure Li4Ti5O12 via a co-precipitation method followed by calcination at 400℃ for 5 h in an Ar atmosphere in order to further investigate the reaction mechanism of the fluoride modification process. Zn2+ and F- co-modified Li4Ti5O12 samples are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and electrochemical measurements. After the modification process, no ZnF2 coating layer is formed on the surface of Li4Ti5O12, instead, F- ions react with Li4Ti5O12 to generate a new phase, composed of a small amount of anatase TiO2, rutile TiO2, LiF, and Zn2+ ions are suspected to form a ZnO coating layer on Li4Ti5O12 particles. The electrolyte reduction decomposition is suppressed in Zn2+ and F- co-modified Li4Ti5O12 due to the ZnO coating layer. 1 wt.% Zn2+ and F- co-modified Li4Ti5O12 exhibits the best rate capability, which leads to a charge capacity of 236.7, 227.8, 222.1, 202.7, 188.9 and 150.7 mAh g -1 at 0.2C, 0.5C, 1C, 3C, 5C and 10C, respectively, between 0 V and 3 V. Furthermore, 1 wt.% Zn2+ and F- comodified Li4Ti5O12 exhibits 96.0% charge capacity retention at 3C rate after 200 cycles, which is significantly higher than that of pure Li4Ti5O12 (78.4%).
Xiaohong Li,Hong-Ling Cui,Rui-Zhou Zhang 한국물리학회 2019 Current Applied Physics Vol.19 No.6
The electronic, mechanical and acoustic properties of Li17Si4-xGex (x=0, 2.3, 3.08, 3.53, and 4) have been investigated by using first-principles calculations based on the density functional theory (DFT). The research shows that the bulk modulus B, Young's modulus E, shear modulus G, and hardness Hv gradually decrease with the increasing Ge content. Li17Si4-xGex have the brittle nature from the analysis of B/G ratio and Cauchy pressure. The maximum Young's moduli are all along [1 1 0] plane, and the sequence of degree of anisotropic property is Li17Ge4 > Li17Si0.48Ge3.52 > Li17Si0.92Ge3.08 > Li17Si1.7Ge2.3 > Li17Si4. The analysis of acoustic velocity shows that all the sound velocities decrease with the increasing Ge content for Li17Si4-xGex (x=0, 2.3, 3.08, 3.53, and 4), and the longitudinal wave along [111] direction is fastest for the studied compounds. Debye temperature ΘD, vt and vl decrease with the increasing Ge content. The minimum thermal conductivity decreases with the increasing Ge content, and Li17Si4-xGex have low thermal conductivities and are not potential thermal conductors. The analysis of electronic properties indicates that Li17Si4-xGex have the metal nature and anisotropic electrical conductivity. The electric conduction is improved with the increasing Ge content.
A polymeric composite protective layer for stable Li metal anodes
Guo Suogang,Wang Li,Jin Yuhong,Piao Nan,Chen Zonghai,Tian Guangyu,Li Jiangang,Zhao Chenchen,He Xiangming 나노기술연구협의회 2020 Nano Convergence Vol.7 No.21
Lithium (Li) metal is a promising anode for high-performance secondary lithium batteries with high energy density due to its highest theoretical specific capacity and lowest electrochemical potential among anode materials. However, the dendritic growth and detrimental reactions with electrolyte during Li plating raise safety concerns and lead to premature failure. Herein, we report that a homogeneous nanocomposite protective layer, prepared by uniformly dispersing AlPO 4 nanoparticles into the vinylidene fluoride-co-hexafluoropropylene matrix, can effectively prevent dendrite growth and lead to superior cycling performance due to synergistic influence of homogeneous Li plating and electronic insulation of polymeric layer. The results reveal that the protected Li anode is able to sustain repeated Li plating/stripping for > 750 cycles under a high current density of 3 mA cm −2 and a renders a practical specific capacity of 2 mAh cm −2 . Moreover, full-cell Li-ion battery is constructed by using LiFePO 4 and protected Li as a cathode and anode, respectively, rendering a stable capacity after 400 charge/discharge cycles. The current work presents a promising approach to stabilize Li metal anodes for next-generation Li secondary batteries.
In-situ PECVD-enabled graphene-V<sub>2</sub>O<sub>3</sub> hybrid host for lithium–sulfur batteries
Song, Yingze,Zhao, Wen,Wei, Nan,Zhang, Li,Ding, Feng,Liu, Zhongfan,Sun, Jingyu Elsevier 2018 Nano energy Vol.53 No.-
<P><B>Abstract</B></P> <P>Lithium–sulfur (Li–S) batteries have been regarded as promising candidates for current energy-storage technologies due to their remarkable advantages in energy density and theoretical capacity. However, one of the daunting challenges remained for advanced Li–S systems thus far deals with the synchronous suppression of polysulfide (LiPS) shuttle and acceleration of redox kinetics. Herein, a cooperative interface bridging adsorptive V<SUB>2</SUB>O<SUB>3</SUB> and conductive graphene is constructed <I>in-situ</I> by virtue of direct plasma-enhanced chemical vapor deposition (PECVD), resulting in the design of a novel V<SUB>2</SUB>O<SUB>3</SUB>-graphene hybrid host to synergize the LiPS entrapment and conversion. The redox kinetics and electrochemical performances of thus-derived cathodes were accordingly enhanced owing to the smooth adsorption-diffusion-conversion of LiPSs even at a sulfur mass loading of 3.7 mg cm<SUP>–2</SUP>. Such interfacial engineering offers us a valuable opportunity to gain insight into the comprehensive regulation of LiPS anchoring ability, electrical conductivity and ion diffusive capability in hybrid hosts on suppressing the LiPS shuttle and propelling the redox kinetics. Our devised PECVD route might pave a new route toward the facial and economic design of hetero-phased multi-functional hosts for high-performance Li–S systems.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Graphene-V<SUB>2</SUB>O<SUB>3</SUB> hybrid host was designed <I>in-situ</I> based on PECVD route. </LI> <LI> Thus-derived cathode showed a low capacity decay of merely 0.046% per cycle at 2 C after 1000 cycles. </LI> <LI> Cathodes with a relatively high sulfur mass loading (3.7 mg cm<SUP>–2</SUP>) were fabricated. </LI> <LI> The smooth adsorption-diffusion-conversion of polysulfides was thoroughly probed <I>via</I> experimental studies and DFT simulations. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>
Shuai Ye,Shuyang Dong,Jun Tan,Le Chen,Hai Yang,Yang Chen,Zeyan Peng,Yingchao Huo,Juan Liu,Mingshan Tang,Yafei Li,Huadong Zhou,Yong Tao 대한신경과학회 2019 Journal of Clinical Neurology Vol.15 No.1
Background and Purpose This study investigated the contribution of white-matter hyperintensities (WMH) and lacunar infarcts (LI) to the risk of Alzheimer’s disease (AD) in an elderly cohort in China. Methods Older adults who were initially cognitively normal were examined with MRI at baseline, and followed for 5 years. WMH were classified as mild, moderate, or severe, and LI were classified into a few LI (1 to 3) or many LI (≥4). Cognitive function was assessed using the Mini Mental State Examination and the Activities of Daily Living scale. Results Among the 2,626 subjects, 357 developed AD by the end of the 5-year follow-up period. After adjusting for age and other potential confounders, having only WMH, having only LI, and having both WMH and LI were associated with an increased risk of developing AD compared with having neither WMH nor LI. Moderate and severe WMH were associated with an increased risk of developing AD compared with no WMH. Furthermore, patients with many LI had an increased risk of developing AD compared with no LI. Conclusions Having moderate or severe WMH and many LI were associated with an increased risk of developing AD, with this being particularly striking when both WMH and LI were present.
Xi-Yang Li,Qian-Lin Chen,Min Yang,Ya-Nan Li,Jing-Bo Ma 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2019 NANO Vol.14 No.3
The lithium titanium spinel Li4Ti5O12 has attracted more and more attention as anode materials applied in lithium ion batteries. Li4Ti5O12 material has been found to be able to intercalate lithium ions without deformation of the lattice. However, compared with graphite and other anode materials, the low conductivity of Li4Ti5O12 restricts its charging and discharging rate. Doping is deemed to be a businesslike method to enhance ionic and electronic conductivity of Li4Ti5O12. This paper reviews the effects of Li4Ti5O12 with different doping ions on different crystal lattice states. And it has been found by a summary that the doping objective of doping ions at Li4Ti5O12 is also different. Moreover, the applications of ion doping in different fields of Li4Ti5O12 are prospected.
Effect of Li Content on the Surface Film Formed on the Binary Mg–Li Alloys in NaCl Solution
Chuanqiang Li,Dahui Liang,Yejia Lin,Yong Dong,Binqing Shi,Changjian Yan,Zhengrong Zhang 대한금속·재료학회 2024 METALS AND MATERIALS International Vol.30 No.1
The surface film formed on the Mg–Li alloys with different Li content in 0.1 M NaCl solution were investigated via electrochemicaltesting, morphologies observation and chemical composition analysis in this work. The results revealed that thesurface film of Mg–14Li alloy (L14: body centred cubic (BCC)) possessed higher electrical resistivity and remained a highertolerating over-potential (0.1 V vs. open circuit potential) than those of Mg–4Li (L4: hexagonal closed-packed (HCP)) andMg–7.5Li (L7: HCP+BCC), resulting in a better corrosion performance. After 24 h immersion in NaCl solution, the wholesurface film of L14 remained undamaged and displayed weave-like and dense characteristic, while both L4 and L7 present aseverely damaged film. The cross-sectional details illustrated typical two layers of surface film formed on L14 with the outerlayer of ~ 1.5 μm and inner layer of ~ 2.5 μm in thickness, whilst only one layer of film with less than 2.5 μm in thicknesswas observed on L4 and L7. At last, combining analysis of X-ray diffraction, energy dispersive X-ray spectrometry, X-rayphotoelectron spectroscopy and transmission electron microscope confirmed the composition of outer layer of surface filmon the L14 contains much more Mg(OH)2 and Li-containing compounds, and the porous Mg(OH)2 film can be sealed by theLi-containing compounds, which is very different the single Mg(OH)2 film on the traditional magnesium and L4/L7 alloys. As a result, the best protective function of the surface film on the L14 alloy contribute to its high corrosion resistance.