A LiFePO4/C composite was synthesized by a simple solid-state reaction method using glucose as reductive agent and carbon source and FePO4 as precursor, which was prepared by introduction of Na3PO4 as phosphorus sourc...A LiFePO4/C composite was synthesized by a simple solid-state reaction method using glucose as reductive agent and carbon source and FePO4 as precursor, which was prepared by introduction of Na3PO4 as phosphorus source and pH regulator in order to pursue lower cost and environmental protection. The structure and morphology of FePO4 and LiFePO4/C were investigated by X-ray diffraction(XRD) and scanning electron microscopy(SEM). Furthermore, electrochemical performance of LiFePO4/C was investigated by galvanostatic charge–discharge tests and cyclicvoltammogram(CV). The results indicate that FePO4 obtained has a small particle size and uniform particle distribution, which is demonstrated to be applicable as the iron source to synthesize LiFePO4/C. Prepared LiFePO4/C shows an excellent rate capability and cycle performance. At rates of 0.1 C, 0.2 C, 1 C and 2 C, the initial discharge capacities of 161, 158, 145 and 120 mAh/g were achieved, respectively and the discharge capacity is 154, 153, 140 and 116 mAh/g after 400 cycles. The employed method of preparing FePO4 by introduction of Na3PO4 has advantages such as low cost, safe raw material, environmental benign and recyclable products, which is suitable for industrial production.展开更多
Well-shaped spherical agglomerates of FePO4 particles were prepared by a novel method:chemical co-precipitation combined with spray-drying.Tap density analysis,Brunauer-Emmett-Teller analysis,characterizations of X-ra...Well-shaped spherical agglomerates of FePO4 particles were prepared by a novel method:chemical co-precipitation combined with spray-drying.Tap density analysis,Brunauer-Emmett-Teller analysis,characterizations of X-ray diffraction,scanning electron microscopy,and transmission electron microscopy confirmed that the micron-sized spherical agglomerates with high specific surface area and high tap density were composed of the uniform nano-sized particles.The effects of pH and reaction time on the morphology of the FePO4 particles were investigated by experimental and theoretical analyses.The analyses revealed that amorphous FePO4 was responsible for forming a well-shaped spherical agglomerate,and the ideal spherical particles were obtained at pH 3.The reaction time also played a significant role in controlling the size and surface morphology of the FePO4 particles,and smooth spherical FePO4 particles were obtained at a reaction time of 6 h.By this novel method,poly-porous spherical iron phosphate particles were prepared,which can be used with high efficiency in some special fields,especially as a precursor for synthesizing LiFePO4 and catalysts.展开更多
Using low-cost FePO4·2H2O as iron source,Na2FePO4F/C composite is prepared by alcohol-assisted ball milling and solid-state reaction method.The XRD pattern of Na2FePO4F/C composite demonstrates sharp peaks,indica...Using low-cost FePO4·2H2O as iron source,Na2FePO4F/C composite is prepared by alcohol-assisted ball milling and solid-state reaction method.The XRD pattern of Na2FePO4F/C composite demonstrates sharp peaks,indicating high crystalline and phase purity.The SEM and TEM images reveal that diameter of the spherical-like Na2FePO4F/C particles ranges from 50 to 300 nm,and HRTEM image shows that the surface of Na2FePO4F/C composite is uniformly coated by carbon layer with a average thickness of about 3.6 nm.The carbon coating constrains the growth of the particles and effectively reduces the agglomeration of nanoparticles.Using lithium metal as anode,the composite delivers a discharge capacities of 102.8,96.4 and 90.3 mA·h/g at rates of 0.5C,1C and 2C,respectively.After 100 cycles at 0.5C,a discharge capacity of 98.9 mA·h/g is maintained with capacity retention of 96.2%.The Li+diffusion coefficient(D)of Na2FePO4F/C composite is calculated as 1.71×10^–9 cm^2/s.This study reveals that the simple solid state reaction could be a practical and effective synthetic route for the industrial production of Na2FePO4F/C material.展开更多
Besides Li＋ and Mg2＋, the electrochemical behavior of Na^＋ and K＋ in LiFePO4/FePO4 structures was studied since they naturally coexist with Li＋ and Mg2＋ in brine. The cyclic voltammogram （CV） results indicated...Besides Li＋ and Mg2＋, the electrochemical behavior of Na^＋ and K＋ in LiFePO4/FePO4 structures was studied since they naturally coexist with Li＋ and Mg2＋ in brine. The cyclic voltammogram （CV） results indicated that Na＋ exhibits some reversibility in LiFePO4/FePO4 structures. Its reduction peak appears at -0.511 V, more negative than that of Li＋ （-0.197 V）, meaning that a relatively positive potential is beneficial for decreasing Na＋ insertion. The reduction peak of K＋ could not be found clearly, indicating that K＋ is difficult to insert into the FePO4 structure. Furthermore, technical experiments using real brine with a super high Mg/Li ratio （493） at a cell voltage of 0.7V showed that the final extracted capacity of Li＋, Mg2＋ and Na＋ that can be attained in 1 g LiFePO4 is 24.1 mg, 7.32 mg and 4.61 mg, respectively. The Mg/Li ratio can be reduced to 0.30 from 493, and the Na/Li ratio to 0.19 from 16.7, which proves that, even in super high Mg/Li ratio brine, if a cell voltage is appropriately controlled, it is possible to separate Li^＋ and other impurities effectively.展开更多
基金Funded by Natural Science Foundation of Hebei Province(No E2017409004)Department of Education of Hebei Province(No QN2016224)
文摘A LiFePO4/C composite was synthesized by a simple solid-state reaction method using glucose as reductive agent and carbon source and FePO4 as precursor, which was prepared by introduction of Na3PO4 as phosphorus source and pH regulator in order to pursue lower cost and environmental protection. The structure and morphology of FePO4 and LiFePO4/C were investigated by X-ray diffraction(XRD) and scanning electron microscopy(SEM). Furthermore, electrochemical performance of LiFePO4/C was investigated by galvanostatic charge–discharge tests and cyclicvoltammogram(CV). The results indicate that FePO4 obtained has a small particle size and uniform particle distribution, which is demonstrated to be applicable as the iron source to synthesize LiFePO4/C. Prepared LiFePO4/C shows an excellent rate capability and cycle performance. At rates of 0.1 C, 0.2 C, 1 C and 2 C, the initial discharge capacities of 161, 158, 145 and 120 mAh/g were achieved, respectively and the discharge capacity is 154, 153, 140 and 116 mAh/g after 400 cycles. The employed method of preparing FePO4 by introduction of Na3PO4 has advantages such as low cost, safe raw material, environmental benign and recyclable products, which is suitable for industrial production.
文摘Well-shaped spherical agglomerates of FePO4 particles were prepared by a novel method:chemical co-precipitation combined with spray-drying.Tap density analysis,Brunauer-Emmett-Teller analysis,characterizations of X-ray diffraction,scanning electron microscopy,and transmission electron microscopy confirmed that the micron-sized spherical agglomerates with high specific surface area and high tap density were composed of the uniform nano-sized particles.The effects of pH and reaction time on the morphology of the FePO4 particles were investigated by experimental and theoretical analyses.The analyses revealed that amorphous FePO4 was responsible for forming a well-shaped spherical agglomerate,and the ideal spherical particles were obtained at pH 3.The reaction time also played a significant role in controlling the size and surface morphology of the FePO4 particles,and smooth spherical FePO4 particles were obtained at a reaction time of 6 h.By this novel method,poly-porous spherical iron phosphate particles were prepared,which can be used with high efficiency in some special fields,especially as a precursor for synthesizing LiFePO4 and catalysts.
基金Projects(51472211,51502256)supported by the National Natural Science Foundation of ChinaProjects(2016GK4005,2016GK4030)supported by the Strategic New Industry of Hunan Province,ChinaProject(13C925)supported by the Research Foundation of Education Bureau of Hunan Province,China
文摘Using low-cost FePO4·2H2O as iron source,Na2FePO4F/C composite is prepared by alcohol-assisted ball milling and solid-state reaction method.The XRD pattern of Na2FePO4F/C composite demonstrates sharp peaks,indicating high crystalline and phase purity.The SEM and TEM images reveal that diameter of the spherical-like Na2FePO4F/C particles ranges from 50 to 300 nm,and HRTEM image shows that the surface of Na2FePO4F/C composite is uniformly coated by carbon layer with a average thickness of about 3.6 nm.The carbon coating constrains the growth of the particles and effectively reduces the agglomeration of nanoparticles.Using lithium metal as anode,the composite delivers a discharge capacities of 102.8,96.4 and 90.3 mA·h/g at rates of 0.5C,1C and 2C,respectively.After 100 cycles at 0.5C,a discharge capacity of 98.9 mA·h/g is maintained with capacity retention of 96.2%.The Li+diffusion coefficient(D)of Na2FePO4F/C composite is calculated as 1.71×10^–9 cm^2/s.This study reveals that the simple solid state reaction could be a practical and effective synthetic route for the industrial production of Na2FePO4F/C material.
基金Project(K1205034-11) supported by Technology Program of Changsha,China
文摘Besides Li＋ and Mg2＋, the electrochemical behavior of Na^＋ and K＋ in LiFePO4/FePO4 structures was studied since they naturally coexist with Li＋ and Mg2＋ in brine. The cyclic voltammogram （CV） results indicated that Na＋ exhibits some reversibility in LiFePO4/FePO4 structures. Its reduction peak appears at -0.511 V, more negative than that of Li＋ （-0.197 V）, meaning that a relatively positive potential is beneficial for decreasing Na＋ insertion. The reduction peak of K＋ could not be found clearly, indicating that K＋ is difficult to insert into the FePO4 structure. Furthermore, technical experiments using real brine with a super high Mg/Li ratio （493） at a cell voltage of 0.7V showed that the final extracted capacity of Li＋, Mg2＋ and Na＋ that can be attained in 1 g LiFePO4 is 24.1 mg, 7.32 mg and 4.61 mg, respectively. The Mg/Li ratio can be reduced to 0.30 from 493, and the Na/Li ratio to 0.19 from 16.7, which proves that, even in super high Mg/Li ratio brine, if a cell voltage is appropriately controlled, it is possible to separate Li^＋ and other impurities effectively.
