|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Disassembly of the fruit cell wall by the ripening-associated polygalacturonase and expansin influences tomato cracking显示文摘Fruit cracking is an important problem in horticultural crop production.Polygalacturonase(SlPG)and expansin(SlEXP1)proteins cooperatively disassemble the polysaccharide network of tomato fruit cell walls during ripening and thereby,enable softening.A Golden 2-like(GLK2)transcription factor,SlGLK2 regulates unripe fruit chloroplast development and results in elevated soluble solids and carotenoids in ripe fruit.To determine whether SlPG,SlEXP1,or SlGLK2 influence the rate of tomato fruit cracking,the incidence of fruit epidermal cracking was compared between wild-type,Ailsa Craig(WT)and fruit with suppressed SlPG and SlEXP1 expression(pg/exp)or expressing a truncated nonfunctional Slglk2(glk2).Treating plants with exogenous ABA increases xylemic flow into fruit.Our results showed that ABA treatment of tomato plants greatly increased cracking of fruit from WT and glk2 mutant,but not from pg/exp genotypes.The pg/exp fruit were firmer,had higher total soluble solids,denser cell walls and thicker cuticles than fruit of the other genotypes.Fruit from the ABA treated pg/exp fruit had cell walls with less water-soluble and more ionically and covalently-bound pectins than fruit from the other lines,demonstrating that ripening-related disassembly of the fruit cell wall,but not elimination of SlGLK2,influences cracking.Cracking incidence was significantly correlated with cell wall and wax thickness,and the content of cell wall protopectin and cellulose,but not with Ca^(2+)content. | Fangling Jiang Alfonso Lopez Shinjae Jeon Sergio Tonetto de Freitas Qinghui Yu Zhen Wu John M.Labavitch Shengke Tian Ann L.T.Powell Elizabeth Mitcham | 2019 | Horticulture Research2019，6，1： | 13 |
| 2 | Hydrogen-assisted scalable preparation of ultrathin Pt shells onto surfactant-free and uniform Pd nanoparticles for highly efficient oxygen reduction reaction in practical fuel cells显示文摘Concentrating active Pt atoms in the outer layers of electrocatalysts is a very effective approach to greatly reduce the Pt loading without compromising the electrocatalytic performance and the total electrochemically active surface area(ECSA)for the oxygen reduction reaction(ORR)in hydrogen-based proton-exchange membrane fuel cells.Accordingly,a facile,low-cost,and hydrogen-assisted two-step method is developed in this work,to massively prepare carbon-supported uniform,small-sized,and surfactant-free Pd nanoparticles(NPs)with ultrathin~3-atomic-layer Pt shells(Pd@Pt_(3L) NPs/C).Comprehensive physicochemical characterizations,electrochemical analyses,fuel cell tests,and density functional theory calculations reveal that,benefiting from the ultrathin Pt-shell nanostructure as well as the resulting ligand and geometric effects,Pd@Pt_(3L) NPs/C exhibits not only significantly enhanced ECSA,electrocatalytic activity,and noble-metal(NM)utilization compared to commercial Pt/C,showing 81.24 m^(2)/gPt,0.710 mA/cm^(2),and 352/577 mA/mgNM/Pt in ECSA,area-,and NM-/Pt-mass-specific activity,respectively;but also a much better electrochemical stability during the 10,000-cycle accelerated degradation test.More importantly,the corresponding 25-cm^(2) H2-air/O_(2) fuel cell with the low cathodic Pt loading of~0.152 mgPt/cm^(2)geo achieves the high power density of 0.962/1.261 W/cm^(2)geo at the current density of only 1,600 mA/cm^(2)geo,which is much higher than that for the commercial Pt/C.This work not only develops a high-performance and practical Pt-based ORR electrocatalyst,but also provides a scalable preparation method for fabricating the ultrathin Pt-shell nanostructure,which can be further expanded to other metal shells for other energy-conversion applications. | Liuxuan Luo Cehuang Fu Aiming Wu Zechao Zhuang Fengjuan Zhu Fangling Jiang Shuiyun Shen Xiyang Cai Qi Kang Zhifeng Zheng Chenyi Hu Jiewei Yin Guofeng Xia Junliang Zhang | 2022 | Nano Research2022，15，3： | 2 |
| 3 | Effects of Eu substituting positions and concentrations on luminescent, dielectric, and magnetic properties of SrTiO3 ceramics 显示文摘 | JIANG C G FANGL SHEN M R ZHENG F G WU X L | 2009 | Applied Physics Letters2009，94，07： | 1 |
| 4 | Temperature-dependent structural changes of[Bmim]FeCl4 magnetic ionic liquid characterized by an in-situ X-ray absorption fine structure显示文摘The temperature-dependent structural changes in 1-butyl-3-methylimidazolium tetrafluoride([Bmim]FeCl4)magnetic ionic liquid(MIL)were investigated by using in-situ X-ray absorption fine structure(XAFS)combined with Raman spectroscopy and DFT calculations.XAFS re sults revealed that the coordination number and bond length of Fe-Cl in the anion of[Bmim]FeCl4 MIL decreased with increments in temperature.These results directly reflected the dissociation of tetrahedral structure[FeCl4]^-,and the formation of bridge-chain[Fe2 Cl5]^+,and[FeCl2]^+species in the anion of[Bmim]FeCl4 MIL.These behaviors indicated that[FeCl4]^-dissociation was endothermic,and was promoted by increased temperature.The results obtained through XAFS were in agreement with those obtained through Raman spectroscopy and DFT calculations. | Fangling Jiang Hao Peng Cheng Li Haiying Fu Guozhong Wu | 2020 | Chinese Chemical Letters2020，31，3： | 1 |
| 5 | Dispersion hydrophobic electrolyte enables lithium-oxygen battery enduring saturated water vapor显示文摘Li-O_(2) batteries gain widespread attention as a can didate for next-generati on energy storage devices due to their extraordinary theoretic specific energy.The semi-open structure of Li-O_(2) batteries causes many parasitic reactions,especially related to water.Water is a double-edged sword,which destroys Li anode and simultaneously triggers a solution-based pathway of the discharge product.In this work,hexamethyldisilazane(HMDS)is introduced into the electrolyte of an aprotic Li-O_(2) battery.HMDS has a strong ability to combine with a trace of water to gen erate a hydrophobic hexamethyldisiloxa ne(MM),which eliminates water from the electrolyte decomposition and then prevents the Li anode from producing the insulating LiOH with water.In this case,the hydrophobic MM disperses in the ether-based electrolyte,forming a dispersion hydrophobic electrolyte.This electrolyte can anchor water from the environment on the cathode side,which triggers a solution-based pathway and regulates the growth morphology of the discharge product and consequently increases the discharge capacity.Compared with the Li-O_(2) battery without the HMDS,the HMDS-containing Li-O_(2) battery contributes an about 13-fold increase of cyclability(400 cycles,1800 h)in the extreme environment of saturated water vapor.This work opens a new approach for directly operating aprotic Li-O_(2) batteries in ambient air. | Yinan Zhang Fangling Jiang Hao Jiang Osamu Yamamoto Tao Zhang | 2022 | Journal of Energy Chemistry2022，31，1： | 0 |
| 6 | Structural analysis of [Bmim]_2CuCl_4 ionic liquids in the presence of water and ethanol by XAFS technique显示文摘The structure of [Bmim]2Cu Cl4 ionic liquids(Bmim: 1-butyl-3-methylimidazolium) with different ratios of H2 O and C2H5 OH was investigated using X-ray absorption fine structure(XAFS) technique. In this study, XAFS was employed to directly probe the conformational variations of copper ions in [Bmim]2Cu Cl4 with the addition of either water or ethanol. XAFS analysis confirmed that the structure of ionic liquids gradually transformed from tetrahedral to octahedral configuration with the increase in ratio of H2 O. Our results also showed that water molecules coordinated with the copper ions of [Bmim]2Cu Cl4, leading to the conformational change in ionic liquids. However, the XAFS spectra of [Bmim]2Cu Cl4/C2H5 OH indicated no coordination of anhydrous ethanol with the copper ions of [Bmim]2Cu Cl4. The structure of [Bmim]2Cu Cl4 ionic liquids is maintained as the tetrahedral configuration in presence of ethanol. Therefore, anhydrous ethanol causes little variation in the structure of ionic liquids and it is a good solvent for the dilution of ionic liquids. | Fangling Jiang Cheng Li Haiying Fu Yaxing Wang Xiaojing Guo Guozhong Wu | 2015 | Science China Chemistry2015，58，4： | 0 |
| 7 | Local Coordination and Reactivity of a Pt Single-Atom Catalyst as Probed by Spectroelectrochemical and Computational Approaches显示文摘The interaction between isolated transition-metal atoms and neighboring dopants in single-atom catalysts(SACs)plays a key role in adsorption strength tuning and catalytic performance engineering.Clarifying the local coordination structures of SACs is therefore of great importance and yet very challenging at the atomic level. | Kun Jiang Xian-Yin Ma Seoin Back Jiajun Zhao Fangling Jiang Xianxian Qin Junliang Zhang Wen-Bin Cai | 2021 | CCS Chemistry2021，3，12： | 0 |
| 8 | A New Comprehensive Evaluation System for Thermo-Tolerance in Tomato at Different Growth Stage显示文摘 | Mintao Sun Fangling Jiang Chuan Zhang Meng Shen Zhen Wu | 2016 | Journal of Agricultural Science and Technology(B)2016，6，3： | 0 |
| 9 | Influence of Fe on electrocatalytic activity of iron-nitrogendoped carbon materials toward oxygen reduction reaction显示文摘The development of highly active nitrogendoped carbon-based transition metal(M-N-C)compounds for the oxygen reduction reaction(ORR)in proton exchange membrane fuel cells(PEMFCs)greatly helps reduce fuel cell cost,thus rapidly promoting their commercial applications.Among different M-N-C electrocatalysts,the series of Fe-N-C materials are highly favored because of their high ORR activity.However,there remains a debate on the effect of Fe,and rare investigations focus on the influence of Fe addition in the second heat treatment usually performed after acid leaching in the catalyst synthesis.It is thus very critical to explore the influences of Fe on the ORR electrocatalytic activity,which will,in turn,guide the design of Fe-N-C materials with enhanced performance.Herein,a series of Fe-N-C electrocatalysts are synthesize and the influence of Fe on the ORR activity are speculated both experimentally and theoretically.It is deduced that the active site lies in the structure of Fe-N4,accompanied with the addition of appropriate Fe,and the number of active sites increases without the occurrence of agglomeration particles.Moreover,it is speculated that Fe plays an important role in stabilizing N as well as constituting active sites in the second pyrolyzing process. | Lin LI Cehuang FU Shuiyun SHEN Fangling JIANG Guanghua WEI Junliang ZHANG | 2022 | Frontiers in Energy2022，16，5： | 0 |
您所在的机构暂未开通此部分的功能，请联系管理员