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| 1 | Comparative Analysis of JmjC Domain-containing Proteins Reveals the Potential Histone Demethylases in Arabidopsis and Rice显示文摘Histone methylation homeostasis is achieved by controlling the balance between methylation and demethylation to maintain chromatin function and developmental regulation. In animals, a conserved Jumonji C (JmjC) domain was found in a large group of histone demethylases. However, it is still unclear whether plants also contain the JmjC domaincontaining active histone demethylases. Here we performed genome-wide screen and phylogenetic analysis of JmjC domain-containing proteins in the dicot plant, Arabidopsis, and monocot plant rice, and found 21 and 20 JmjC domaincontaining, respectively. We also examined the expression of JmjC domain-containing proteins and compared them to human JmjC counterparts for potential enzymatic activity. The spatial expression patterns of the Arabidopsis JmjC domaincontaining genes revealed that they are all actively transcribed genes. These active plant JmjC domaincontaining genes could possibly function in epigenetic regulation to antagonize the activity of the large number of putative SET domaincontaining histone methyltransferase activity to dynamically regulate histone methylation homeostasis. | Falong Lu Guanglin Li Xia Cui Chunyan Liu Xiu-Jie Wang Xiaofeng Cao | 2008 | Journal of Integrative Plant Biology2008，50，7： | 24 |
| 2 | One-step uniform growth of magnesium hydride nanoparticles on graphene显示文摘A simple solvent-free method to synthesize MgH_2 nanoparticles(MgH_2NPs) uniformly grown on graphene nanosheets(GNs) has been reported in this paper. Based on the formation of MgH_2 by di-n-butylmagnesium((C_4H_9)_2Mg) thermal decomposition under hydrogen pressure, the GNs were added as matrix to hinder the agglomeration and growing of MgH_2NPs. The fabricated MgH_2/GNs nanocomposites, in which MgH_2 NPs were homogenously growing in the graphene matrix, have been synthesized by the favorable adsorption energy between(C_4H_9)_2Mg and GNs. Resulting from the one-step solvent-free route, the generated MgH_2 NPs shows high hydrogen capacity and steady hydriding and dehydriding properties, without the interference of the synthetic medium. At the same time, the size of the fabricated MgH_2NPs can be controlled by adjusting the mass ratio of MgH_2 to graphene, the various hydrogen pressure and temperature. Attributed to smaller size effect, well uniform distribution of high density MgH_2NPs, and the agglomeration blocking ability of graphene,the MgH_2/GNs-40 wt% exhibits the favorite hydrogen storage performance. | Yuqin Huang Guanglin Xia Jie Chen Baoping Zhang Qian Li Xuebin Yu | 2017 | Progress in Natural Science:Materials International2017，27，1： | 5 |
| 3 | A balance between catalysis and nanoconfinement towards enhanced hydrogen storage performance of NaAlH_(4)显示文摘Owing to its favorable thermodynamics and high density,NaAlH_(4) has been widely regarded as a potential hydrogen storage material,but its practical application is hindered by the sluggish kinetics,high operating temperature and poor cycling stability.Here,taking advantage of Co-doped nanoporous carbon scaffolds as structural host,we develop a new strategy to balance the synergistic effect between the catalytic role of Co nanoparticles and the nanoconfinement role of porous carbon scaffolds via the controllable etching of Co nanoparticles towards enhanced hydrogen storage performance of NaAlH_(4).The etching of Co nanoparticles creates extra void spaces nearby catalytically active Co nanoparticles,which not only exerts the catalytic effect of Co nanoparticles,but also improves the nanoconfinement role in maintaining the cycling stability towards increased loading ratio and hence high systematic capacity.Induced by this balanced synergistic effect,the peak temperature for the dehydrogenation of NaAlH_(4) could be reduced to 164°C,97°C lower than the bulk counterpart,even under an ultrahigh loading ratio of 67%,and more importantly,the reversible systematic hydrogen storage capacity could still reach 3.3 wt.%after 5 cycles.This work opens up a new avenue to improve the hydrogen storage performance of various complex hydrides. | Wei Chen Lei You Guanglin Xia Xuebin Yu | 2021 | Journal of Materials Science & Technology2021，，20： | 1 |
| 4 | Changes of immunocytic phenotypes and functions from human colorectal adenomatous stage to cancerous stage: Update显示文摘 | Yanhong Shi Zhenfeng Li Wei Zheng Xia Liu Chenyi Sun Jann-Birger Laugsand Zhanju Liu Guanglin Cui | 2015 | Immunobiology2015，，10： | 1 |
| 5 | Magnesium hydride nanoparticles anchored on MXene sheets as high capacity anode for lithium-ion batteries显示文摘Magnesium hydride, with high specific capacity, favorable voltage profile and low voltage hysteresis properties, is regarded as a promising anode for lithium storage. However, the rapid fading of capacity caused by huge volume change, low electron/ion conduction, and spontaneous agglomeration of active materials during cycling greatly limit its practical application in lithium-ion batteries. Herein, we report the synthesis of monodisperse MgH2 nanoparticles with an average particle size of <20 nm homogeneously anchored on Ti3C2 MXene sheets by bottom-up self-assembly strategy. The unique nanoarchitectures are able to efficiently enhance the lithium insertion/extraction kinetics, accelerate the electron/lithium ion transfer and buffer the strain of volume changes. More importantly, the formed F–Mg bounding between MgH2 and MXene could avoid the shedding of MgH2 nanoparticles to electrolyte during cycling, which significantly enhance the capacity, cyclability, and rate performance of magnesium hydride. Moreover, due to the high density of MXene and the synergistic effect between the MgH2 and MXene matrix, the MgH2/MXene composite with 60 wt% MgH2 delivers a superior volumetric capacity of 1092.9 mAh cm−3 at a current density of 2000 mA g^(−1) after 1000 cycles. These results highlight the great promising of MgH2/MXene composite for high performance lithium-ion batteries. | Shulin Zhong Shunlong Ju Yifei Shao Wei Chen Tengfei Zhang Yuqin Huang Hongyu Zhang Guanglin Xia Xuebin Yu | 2021 | Journal of Energy Chemistry2021，30，11： | 1 |
| 6 | Hydro- gen release from amminelithium borohydride, LiBH4 ~ NH3 显示文摘 | Guo Yanhui Xia Guanglin Zhu Yihan | 2010 | Chemical Communications2010，46，15： | 1 |
| 7 | Ion diffusion,and hysteresis of magnesium hydride conversion electrode materials显示文摘MgH_(2),owing to a high theoretical capacity of 2038 mAh g^(−1),is regarded as a promising anode material for lithium-ion batteries(LIBs).However,the application of MgH_(2) is still far from satisfactory due to its poor cycling stability.Herein,nano-crystallization of MgH_(2) as an anode is applied for all-solid-state lithium-ion batteries(ASSLIBs)using LiBH4 as a solid-state electrolyte.The self-assembly designed MgH_(2) electrode on graphene could effectively alleviate the volume expansion,prevent the agglomeration of active substances,improve the electron transfer,and enhance the electrochemical performance of the anode material.As a result,a reversible capacity of 1214 mAh g^(−1) after 50 cycles is obtained.Significantly enhanced cycle life with a notable capacity of 597 mAh g^(−1) at a current density of 400 mA g^(−1) is delivered after 200 cycles.Further investigation on full cells also exhibits great application potential on ASSLIBs. | Yingtong Lv Xiang Zhang Wei Chen Shunlong Ju Zhenhua Liu Guanglin Xia Takayuki Ichikawa Tengfei Zhang Xuebin Yu | 2023 | Journal of Materials Science & Technology2023，，24： | 0 |
| 8 | Atomic scale understanding of aluminum intercalation into layered TiS2 and its electrochemical properties显示文摘Aluminum-ion batteries (AIBs) are attracting great attentions recently because of the high volumetric capacity,natural abundance of Al and operational safety.Using metallic A1 as anode,the development of suitable cathode materials is a key issue to build an advanced AIBs system [1,2].Up to now,various materials have been studied as cathode materials for AIBs,including graphite [3,4],metal oxides [5-7],and metal sulfides [8,9].However,few of them can meet the application requirements,and the theoretical understanding of their electrochemical mechanism is limited. | Shunlong Ju Xiaowei Chen Zunxian Yang Guanglin Xia Xuebin Yu | 2020 | Journal of Energy Chemistry2020，29，4： | 0 |
| 9 | Synergistic effect of lithiophilic Zn nanoparticles and N-doping for stable Li metal anodes显示文摘Li metal is the most ideal anode material for next-generation high energy lithium-ion batteries.The uncontrollable growth of Li dendrites,however,hinders its practical application.Herein,we propose the adoption of Zn nanoparticles uniformly embedded in N-doped carbon polyhedra homogeneously built on carbon cloth(Zn@NC@CC)to prevent the formation of Li dendrites.Based on theoretical calculation and experimental observation,lithiophilic Zn nanoparticles and N-doping inside of the assynthesized Zn@NC play a synergistic role in enhancing the adsorption capacity with Li,thus resulting in uniform Li deposition and complete suppression of Li dendrites.Moreover,the porous N-doped carbon polyhedras uniformly distributed on carbon cloth effectively relieves the volume change of Li upon repeated Li stripping/plating process,which contributes to preserving the structural integrity of the whole electrode and hence enhancing its long-term cycling stability.Benefiting from these synergistic effects,the Li-Zn@NC@CC electrode delivers a prolonged lifespan of over 1200 h at 1 mA cm^(-2) with an areal capacity of 1 mA h cm^(-2) in symmetric cells and high Coulombic efficiencies of 95.4%under an ultrahigh capacity of 12 mA h cm^(-2).Remarkably,Li-Zn@NC@CC//LiFePO_(4) full cells deliver a high reversible capacity of 110.2 mA h g^(-1) at 1 C over 200 cycles. | Lei You Shunlong Ju Jianwen Liu Guanglin Xia Zaiping Guo Xuebin Yu | 2022 | Journal of Energy Chemistry2022，31，2： | 0 |
| 10 | Niobium fluoride-modified hydrogen evolution reaction of magnesium borohydride diammoniate显示文摘Metal borohydride ammoniates have become one of the most promising hydrogen storage materials due to their ultrahigh capacities.However,their application is still restricted by the high temperature of hydrogen desorption and the release of ammonia.Here,to promote the dehydrogenation evolution and suppress the ammonia release,different amounts of NbF 5 were introduced into Mg(BH4)2·2NH3.Compared to the pure Mg(BH_(4))_(2)·2NH_(3),the Mg(BH_(4))_(2)·2NH_(3)-NbF_(5) composites exhibit lower onset dehydriding temperatures(53–57℃)and higher dehydriding capacities(5.6 wt.%–8.2 wt.%)at below 200℃,with the complete suppression of ammonia.In addition,7.4 wt.%H_(2) could be released from Mg(BH_(4))_(2)·2NH_(3)–5 mol%NbF5 composite at 200℃ within 20 min and the apparent activation energy is calculated to be 60.28 kJ mol^(-1),which is much lower than that of pure Mg(BH_(4))_(2)·2NH_(3)(92.04 kJ mol^(-1)).Mg(BH_(4))_(2)·2NH_(3) should mechanochemically react with NbF5,forming dual-metal(Mg,Nb)borohydride ammoniate and spherical MgF2.The introduction of electronegative Nb cation results in-situ formation of(Mg,Nb)borohydride ammoniate towards a lower dehydrogenation temperature and a higher hydrogen release purity.The increased phase boundaries among the Mg(BH_(4))_(2)·2NH_(3),dual-metal(Mg,Nb)borohydride ammoniate,and MgF2 phases further facilitate the hydrogen diffusion during the dehydrogenation of the composites. | Yujie Lv Bao Zhang Haixiang Huang Bogu Liu Wei Lv Jianguang Yuan Guanglin Xia Xuebin Yu Dalin Sun Ying Wu | 2023 | Journal of Materials Science & Technology2023，，25： | 0 |
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