In this study,sub-micrometer LiFePO_4 particles with high purity and crystallinity were synthesized using supercritical hydrothermal method as the cathode material for lithium ion batteries.Experimental results show t...In this study,sub-micrometer LiFePO_4 particles with high purity and crystallinity were synthesized using supercritical hydrothermal method as the cathode material for lithium ion batteries.Experimental results show that templates and calcination time have significant impacts on the purity,particle size and morphology of LiFePO_4 particles.The as-prepared LiFePO_4 particles using polyvinyl pyrrolidone(PVP) template with additional one hour calcination at 700℃exhibit characteristics of good crystallinity,uniform size distribution,high capacity and cycling performance.The specific discharge capacities of 141.2 and 114.0mA·h/g were obtained at the charge/discharge rates of 0.1 and 1.0 C,respectively.It retained 96.0%of an initial capacity after 100 cycles at 1.0 C rate.The good electrochemical performance of the as-synthesized material is attributed to the synergistic factors of its reasonable particle size and surface areas and high crystallinity.展开更多
Synthesis of the spinel structure lithium manganese oxide （LiMn2O4） by supercritical hydrothermal （SH） accelerated solid state reaction （SSR） route was studied. The impacts of the reaction pressure, reaction tem...Synthesis of the spinel structure lithium manganese oxide （LiMn2O4） by supercritical hydrothermal （SH） accelerated solid state reaction （SSR） route was studied. The impacts of the reaction pressure, reaction temperature and reaction time of SH route, and the calcination temperature of SSR route on the purity, particle morphology and electrochemical properties of the prepared LiMn2O4 materials were studied. The experimental results show that after 15 min reaction in SH route at 400 ℃ and 30 MPa, the reaction time of SSR could be significantly decreased, e.g. down to 3 h with the formation temperature of 800 ℃, compared with the conventional solid state reaction method. The prepared LiMn2O4 material exhibits good crystallinity, uniform size distribution and good electrochemical performance, and has an initial specific capacity of 120 mA.h/g at a rate of 0.1C （1C=148 mA/g） and a good rate capability at high rates, even up to 50C.展开更多
A new compound, [Eu（Hcit）（H2O）2]·H2O]n （1, Hcit^3-= C（OH）（COO-）（CH2COO-）2）, has been synthesized under hydrothermal reactions of europium oxide, MnCl2·4H2O and citric acid at 120 ℃ for three day...A new compound, [Eu（Hcit）（H2O）2]·H2O]n （1, Hcit^3-= C（OH）（COO-）（CH2COO-）2）, has been synthesized under hydrothermal reactions of europium oxide, MnCl2·4H2O and citric acid at 120 ℃ for three days. The compound was characterized by single-crystal X-ray diffraction analyses, IR and TGA. Complex 1 crystallizes in monoclinic, space group P21/n with a = 6.179（1）, b = 9.688（2）, c = 16.990（3） A, β = 91.98（3）°, Z = 4, V = 1016.4（3） A^3, C6H11EuO10, Mr = 395.11, Dc = 2.582 g/cm3, μ = 6.218 mm-1, F（000） = 760, R = 0.0183 and wR = 0.0411. Single-crystal X-ray analysis reveals that complex 1 displays 1D ladder chains along the a axis, with dinuclear Eu2O2 units serving as ＂steps＂ and carboxylate groups as ＂uprights＂, which are connected by hydrogen bonds. The solid-state luminescent property of complex 1 was investigated at room temperature. Upon excitation at 394 nm, compound 1 exhibits interesting luminescent properties with several intense bands in the visible region and the most intense and sharp emission being in the red region at 615 nm. The TGA and XRD results prove that complex 1 undergoes facile thermal decomposition to form Eu2O3 at about 870 ℃.展开更多
基金the Fundamental Research Funds for the Central Universities of China(No.DUT11NY08)
文摘In this study,sub-micrometer LiFePO_4 particles with high purity and crystallinity were synthesized using supercritical hydrothermal method as the cathode material for lithium ion batteries.Experimental results show that templates and calcination time have significant impacts on the purity,particle size and morphology of LiFePO_4 particles.The as-prepared LiFePO_4 particles using polyvinyl pyrrolidone(PVP) template with additional one hour calcination at 700℃exhibit characteristics of good crystallinity,uniform size distribution,high capacity and cycling performance.The specific discharge capacities of 141.2 and 114.0mA·h/g were obtained at the charge/discharge rates of 0.1 and 1.0 C,respectively.It retained 96.0%of an initial capacity after 100 cycles at 1.0 C rate.The good electrochemical performance of the as-synthesized material is attributed to the synergistic factors of its reasonable particle size and surface areas and high crystallinity.
基金Project supported by the Research Funds of the Key Laboratory of Fuel Cell Technology of Guangdong Province,ChinaProject(7411793079907)supported by the Guangzhou Special Foundation for Applied Basic Research+1 种基金Project(2013A15GX048)supported by the Dalian Science and Technology Project Foundation,ChinaProject(21376035)supported by the National Natural Science Foundation of China
文摘Synthesis of the spinel structure lithium manganese oxide （LiMn2O4） by supercritical hydrothermal （SH） accelerated solid state reaction （SSR） route was studied. The impacts of the reaction pressure, reaction temperature and reaction time of SH route, and the calcination temperature of SSR route on the purity, particle morphology and electrochemical properties of the prepared LiMn2O4 materials were studied. The experimental results show that after 15 min reaction in SH route at 400 ℃ and 30 MPa, the reaction time of SSR could be significantly decreased, e.g. down to 3 h with the formation temperature of 800 ℃, compared with the conventional solid state reaction method. The prepared LiMn2O4 material exhibits good crystallinity, uniform size distribution and good electrochemical performance, and has an initial specific capacity of 120 mA.h/g at a rate of 0.1C （1C=148 mA/g） and a good rate capability at high rates, even up to 50C.
基金supported by the Fundamental Research Funds for the Central Universities,SCUT (No. 2009ZM0313)the National Natural Science Foundation of China (B5080320)
文摘A new compound, [Eu（Hcit）（H2O）2]·H2O]n （1, Hcit^3-= C（OH）（COO-）（CH2COO-）2）, has been synthesized under hydrothermal reactions of europium oxide, MnCl2·4H2O and citric acid at 120 ℃ for three days. The compound was characterized by single-crystal X-ray diffraction analyses, IR and TGA. Complex 1 crystallizes in monoclinic, space group P21/n with a = 6.179（1）, b = 9.688（2）, c = 16.990（3） A, β = 91.98（3）°, Z = 4, V = 1016.4（3） A^3, C6H11EuO10, Mr = 395.11, Dc = 2.582 g/cm3, μ = 6.218 mm-1, F（000） = 760, R = 0.0183 and wR = 0.0411. Single-crystal X-ray analysis reveals that complex 1 displays 1D ladder chains along the a axis, with dinuclear Eu2O2 units serving as ＂steps＂ and carboxylate groups as ＂uprights＂, which are connected by hydrogen bonds. The solid-state luminescent property of complex 1 was investigated at room temperature. Upon excitation at 394 nm, compound 1 exhibits interesting luminescent properties with several intense bands in the visible region and the most intense and sharp emission being in the red region at 615 nm. The TGA and XRD results prove that complex 1 undergoes facile thermal decomposition to form Eu2O3 at about 870 ℃.
