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| 1 | Redistribution of Li-ions using covalent organic frameworks towards dendrite-free lithium anodes:a mechanism based on a Galton Board显示文摘Because of its high theoretical specific capacity and low reduction potential,Li metal is considered to be key to reaching high energy density in rechargeable batteries.In this context,most of the research has focused on suppressing dendrite formation during Li deposition to improve the cycling reversibility and safety of the batteries.Here,covalent organic framework(COF)film coating on a commercial polypropylene separator is applied as an ion redistributor to eliminate Li dendrites.The COF crystallites consist of ordered nanochannels that hinder the movement of anions while allowing Li-ions to transport across,leading to a high Li-ion transference number of 0.77±0.01.The transport of Li-ions across the COF film can be considered to be analogous to beads passing through a Galton Board,a model that demonstrates a statistical concept of a normal distribution.Thus,an even distribution of Li-ions is obtained at the COF/Li metal interface.The controlled Li-ion flux yields a smooth Li metal surface after 1,000 h(500 times)of cycling,leading to a significantly improved cycling stability and reversibility,as demonstrated by Cu||Li half cells,Li||Li symmetric cells,and Li Fe PO4||Li full cells.These results suggest that,following the principle of a Galton Board,nanopore insulators such as COF-based materials are effective ion distributors for the different energy storage or conversion systems. | Huanyu Xie Qing Hao Hongchang Jin Shuai Xie Zhaowei Sun Yadong Ye Chaohui Zhang Dong Wang Hengxing Ji Li-Jun Wan | 2020 | Science China Chemistry2020，63，9： | 3 |
| 2 | SPINDLY, ERECTA, and Its Ligand STOMAGEN Have a Role in Redox-Mediated Cortex Proliferation in the Arabidopsis Root显示文摘反应的氧种类(ROS ) 对所有生活有机体有害,因此,他们必须被移开保证正常生长和开发。ROS 也正在表明分子,但是到目前为止,很少在植物对 ROS 感觉和发展反应的机制被知道。我们这里报导那氢过氧化物在 Arabidopsis 根和那导致外皮增长细长纤弱(间谍) ,连接 O 的 glucosamine acetyltransferase,由维持细胞的氧化还原作用动态平衡调整外皮增长。我们也发现在充满白氨酸的受体 kinase ERECTA 和它的通常认为的肽 ligand STOMAGEN 的变化在根外皮增长上堵住氢过氧化物的效果。然而,而额外的外皮房间从内皮被生产, ERECTA 和 STOMAGEN 在脉管的织物被表示,建议细胞间的发信号的参与。间谍 ERECTA 显得行动下游,因为间谍变化仍然在 erecta 异种背景引起了外皮增长。我们因此有不仅获得了卓见进由哪个间谍调整根开发的机制而且揭开为在植物发信号的 ROS 的一条新奇小径。对氧化应力的保护的机制也被讨论的调停氧化还原作用的外皮增长的重要性。 | Hongchang Cui Danyu Konga Pengcheng Wei Yueling Hao Keiko U. Torii Jin Suk Lee Jie Li | 2014 | Molecular Plant2014，7，12： | 2 |
| 3 | Monitoring the mechanical properties of the solid electrolyte interphase(SEI)using electrochemical quartz crystal microbalance with dissipation显示文摘Stable solid electrolyte interphase(SEI)has been well established to be critical for the reversible operation of Li(ion)batteries,yet our understanding of its mechanical properties currently remains incomplete.Here,we used an electrochemical quartz crystal microbalance combined with dissipation monitoring(EQCM-D)to investigate SEI formation.By quantitatively estimating in-situ,the change in mass,shear modulus,and viscosity of the SEI,we show that the SEI formation in propylene carbonate(PC)-and ethylene carbonate/diethyl carbonate(EC/DEC)-based electrolytes involves the growth of a rigid laye r followed by a viscoelastic layer,whereas a distinct'one-layer'rigid model is applicable to the SEI formulated in tetraethylene glycol dimethyl ether(TEGDME)-based electrolyte.With the continuous formation of the SEI,its shear modulus decreases accompanied by an increase in viscosity.In TEGDME,the lightest/thinnest SEI(mass lower than in PC by a factor of nine)yet having the greatest stiffness(more than five times that in PC)is obtained.We attribute this behavior to differences in the chemical composition of the SEIs,which have been revealed by tracking the mass-change-per-mole-of-electrontransferred using EQCM-D and further confirmed by X-ray photoelectron spectroscopy. | Yinguang Chai Wenshan Jia Zhiqiu Hu Song Jin Hongchang Jin Huanxin Ju Xingbin Yan Hengxing Ji Li-Jun Wan | 2021 | Chinese Chemical Letters2021，32，3： | 2 |
| 4 | Cobalt and nitrogen atoms co-doped porous carbon for advanced electrical double-layer capacitors显示文摘Electrical double-layer capacitors are widely concerned for their high power density,long cycling life and high cycling efficiency.However,their wide application is limited by their low energy density.In this study,we propose a simple yet environmental friendly method to synthesize cobalt and nitrogen atoms co-doped porous carbon(CoAT-NC) material.Cobalt atoms connected with primarily pyridinic nitrogen atoms can be uniformly dispersed in the amorphous carbon matrix,which is benefit for improving electrical conductivity and density of states of the carbon material.Therefore,an enhanced perfo rmance is expected when CoAT-NC is served as electrode in a supercapacitor device.CoAT-NC displays a good gravimetric capacitance of 160 F/g at 0.5 A/g combing with outstanding capacitance retention of 90% at an extremely high current density of 100 A/g in acid electrolyte.Furthermore,a good energy density of 30 Wh/kg can be obtained in the organic electrolyte. | Aiqin Xiang Shuai Xie Fei Pan Hongchang Jin Yiheng Zhai Yanwu Zhu Xianghua Kong Hengxing Ji | 2021 | Chinese Chemical Letters2021，32，2： | 2 |
| 5 | NS codoped carbon nanorods as anode materials for high-performance lithium and sodium ion batteries显示文摘NS codoped carbon nanorods(NS-CNRs) were prepared using crab shell as template and polyphenylene sulfide(PPS) as both the C and S precursor, followed by carbonization in NH_3. The as-obtained NS-CNRs had a diameter of ~50 nm, length of several micrometers, and N and S contents of 12.5 at.% and 3.7 at.%,respectively, which can serve as anodes for both lithium-ion batteries(LIBs) and sodium ion batteries(SIBs). When serving as an anode of LIB, the NS-CNRs delivered gravimetric capacities of 2154 mAh g^(-1)at current densities of 0.1 A g^(-1)and 625 mAh g^(-1)at current densities of 5.0 A g^(-1)for 1000 cycles.When serving as an anode of SIB, the NS-CNRs delivered gravimetric capacities of 303 mAh g^(-1)at current densities of 0.1 A g^(-1)and 230 mAh g^(-1)at current densities of 1.0 A g^(-1)for 3000 cycles. The excellent electrochemical performance of NS-CNRs could be ascribed to the one-dimensional nanometer structure and high level of heteroatom doping. We expect that the obtained NS-CNRs would benefit for the future development of the doped carbon materials for lithium ion batteries and other extended applications such as supercapacitor, catalyst and hydrogen storage. | Ajuan Hu Song Jin Zhenzhen Du Hongchang Jin Hengxing Ji | 2018 | Journal of Energy Chemistry2018，27，1： | 1 |
| 6 | Photosynthetic rate, chlorophyll fluorescence parameters, and lipid peroxidation of maize leaves as affected by zincdeficiency显示文摘 | Wang Hongchang Jin Jiyun | 2005 | Photosynthetica2005，43，4： | 1 |
| 7 | Regulating Li transport in Li-magnesium alloy for dendrite free Li metal anode显示文摘Li metal has become a strong candidate for anode due to its high theoretical specific capacity and lowest electrochemical potential.However,the poor reversibility caused by continuous chemical and electrochemical degradation hinders the practical application of Li metal.Solid-solution-based metal alloy phases have been proposed as hosts for regulating the non-dendrite electrodeposition,but the fundamental understanding remains unclear due to the drastically different deposition behaviors of Li on them.Here we found the difference in the diffusion coefficient of Li atoms on solid-solution-based metal alloy phases(Li-Mg and Li-Ag alloys)was a major contributor to the different deposition behaviors.The low Li atom diffusion coefficient of Li-Mg alloy showed a preferential Li accumulation on the upper surface rather than the inward-growth plating of Li atoms into alloy foil in Li-Ag alloy.By the process of secondary recrystallization,we improved the diffusion coefficient of Li atoms in Li-Mg alloy that facilitates the inward transfer rather than surface plating of Li atoms.In this case,the recrystallized Li-Mg alloy underwent a solidsolution phase change in the delithiation-lithiation cycles which yielded a high Coulombic efficiency of 99.3%with a reversible gravimetric capacity of 2,874 mAh·g−1 and superior cycling stability over 5,000 h without dendrite growth. | Jinxi Wang Yadong Ye Hongmin Zhou Wei Zhang Zhaowei Sun Jiawen Zhu Hongchang Jin Huanyu Xie Haoliang Huang Yi Cui Rong Huang Zezhong Li Song Jin Hengxing Ji | 2023 | Nano Research2023，16，6： | 0 |
| 8 | TiN nanocrystal anchored on N-doped graphene as effective sulfur hosts for high-performance lithium-sulfur batteries显示文摘Lithium-sulfur(Li-S)batteries have become prospective candidates for next-generation energy storage owing to the high energy density and low cost.However,the sluggish kinetics of the electrochemical reaction and shuttle effect result in a rapid capacity decay.Herein,a titanium nitride nanocrystal/Ndoped graphene(TiN@NG)composite is developed to host elemental sulfur.The TiN nanoparticles decorated on graphene sheets attract Li polysulfides(LiPSx)and catalyze the electrochemical reduction and oxidation of LiPSx in the discharge and charge processes,respectively.These two effects effectively restrain the dissolution of the LiPSx and accelerate the electrochemical reactions,thereby,alleviating the shuttle effect.As a result,the cathode composed of TiN@NG/S delivers a remarkable reversible capacity(1390 mA h g^(-1) at 0.1 C)and excellent cycling performance(730 mA h g^(-1) after 300 cycles).We believe that this work can bring some inspiration for designing high-performance Li-S batteries. | Wenmiao Chen Hongchang Jin Shuai Xie Huanyu Xie Junfa Zhu Hengxing Ji Li-Jun Wan | 2021 | Journal of Energy Chemistry2021，30，3： | 0 |
| 9 | A comparison study on single metal atoms(Fe,Co,Ni)within nitrogen-doped graphene for oxygen electrocatalysis and rechargeable Zn-air batteries显示文摘Single atom catalysts(SACs)with atomically dispersed transition metals on nitrogen-doped carbon supports have recently emerged as highly active non-noble metal electrocatalysts for oxygen reduction reaction(ORR)and oxygen evolution reaction(OER),showing great application potential in Zn-air batteries.However,because of the complex structure-performance relationships of carbon-based SACs in the oxygen electrocatalytic reactions,the contribution of different metal atoms to the catalytic activity of SACs in Zn-air batteries still remains ambiguous.In this study,SACs with atomically dispersed transition metals on nitrogen-doped graphene sheets(M-N@Gs,M=Co,Fe and Ni),featured with similar physicochemical properties and M-N@C configurations,are obtained.By comparing the on-set potentials and the maximum current,we observed that the ORR activity is in the order of Co-N@G>Fe-N@G>Ni-N@G,while the OER activity is in the order of Co-N@G>Ni-N@G>Fe-N@G.The Zn-air batteries with Co-N@G as the air cathode catalysts outperform those with the Fe-N@G and Ni-N@G.This is due to the accelerated charge transfer between Co-N@C active sites and the oxygen-containing reactants.This study could improve our understanding of the design of more efficient bifunctional electrocatalysts for Zn-air batteries at the atomic level. | Shuai Xie Hongchang Jin Chao Wang Huanyu Xie Ying-Rui Lu Ting-Shan Chan Wensheng Yan Song Jin Hengxing Ji | 2023 | Chinese Chemical Letters2023，34，6： | 0 |
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