Polyvinyl pyrrolidone-assisted synthesis of a Fe3O4/graphene composite with excellent lithium storage properties

Key Project of NSFC [U1305246, 21321062]; Xiamen city [3502Z20121002]This paper reports a weak interaction between metal oxide and graphene in the Fe3O4/graphene composite, which results in the superior electrochemical performance

Polyvinyl pyrrolidone-assisted synthesis of a Fe3O 4/graphene composite with excellent lithium storage properties

This paper reports a weak interaction between metal oxide and graphene in the Fe3O4/graphene composite, which results in the superior electrochemical performance. ? 2014 The Royal Society of Chemistry

Hierarchical structure LiFePO4@C synthesized by oleylamine-mediated method for low temperature applications

NSFC [U1305246, 21321062]; Major Project; Xiamen city [3502Z20121002]In this paper, a hierarchical nanostructure LiFePO4@C composite was firstly fabricated by an oleylamine mediated method. The oleylamine played a multifunctional role in restricting the particle size and forming the porous nano-structure of LiFePO4@C composite. Benefiting from its hierarchical structure, LiFePO4@C exhibited superior electrochemical performance, especially at low temperature. It can deliver a capacity of 117 mA h g(-1) at a current density of up to 700 mA g(-1) (about 5 C) at -20 degrees C

Study on SnO2/graphene composites with superior electrochemical performance for lithium-ion batteries

NSFC [U1305246, 21321062]; Xiamen city [3502Z20121002]; Quanzhou "Tong-Jiang Scholar" program; Fujian "Min-Jiang Scholar" program; program for New Century Excellent Talents in University [NCET-13-0879]; Education and Scientific Research Foundation (Class A) for Young Teachers of Education Bureau of Fujian Province, China [JA13263]; National Natural Science Foundation of China [21353001]In this study, the in situ growth of tin dioxide (SnO2) nanoparticles on reduced graphene oxide (rGO) has been realized using a hydrothermal method. The size of the SnO2 nanoparticles in the SnO2/rGO composites prepared by three different procedures is about 5 nm, and they are well dispersed on rGO. When applied as anode materials for lithium-ion batteries, we found that the composites synthesized from the stannous oxalate precursor showed the best rate performance and highest cyclic stability. The surface status of the composites, including interactions between SnO2 and rGO and surface chemical components, was investigated in detail in order to understand why the composites prepared using different procedures displayed vastly different electrochemical performances. The results presented here describe a new approach for the synthesis of uniform and nanosized metal-oxide/rGO composites with excellent electrochemical performance

Preparation and characterization of a novel composite microporous polymer electrolyte for Li-ion batteries

A novel composite microporous polymer electrolyte composed of poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP) and mesoporous SBA-15 was prepared. The composite solid polymer electrolyte (CSPE) exhibits ionic conductivity as high as 0.30 mS-(cm-1) with a composition of SBA-15 : PVdF-HFP=3 : 8 at room temperature. Infrared transmission spectroscopic results suggested that the mechanism of micropore formation is similar to that of the phase inversion. X-ray diffraction (XRD) results demonstrated that the addition of SBA-15 inhibits the crystallization of PVdF-HFP, while the SBA-15 preserves well its ordered mesoporous structure during the course of preparation. The Li/CSPE/MCF of half-cell was assembled, and it showed a good electrochemical and cyclability performance during charge-discharge cycles

Studies of the first lithiation of graphite materials by electrochemical impedance spectroscopy

First lithiation of graphite electrode in 1 mol/L LiPF6-EC:DEC:DMC electrolyte was investigated by electrochemical impedance spectroscopy (EIS). The results illustrated that the first arc in the high-frequency range observed in the Nyquist diagram appears near 0.9 V in the initial lithiation of graphite electrode, and its diameter increases with the decrease of polarization potential. These EIS features were attributed to the formation and growth of SEI film. Appropriate equivalent circuit was proposed to fit the experimental EIS data. The fitting results revealed the process of the formation and growth of SEI film, and evaluated quantitatively the resistance of charge transfer, as well as the capacitance of double layer along with the increase of polarization potentials

Solid-state thin film li-ion batteries

Thin film lithium batteries based on polymer electrolytes and solid-state inorganic electrolytes are introduced in this article. We mainly review the progress of the all-solid-state thin film lithium batteries based on inorganic electrolytes, including the preparation methods and the properties of the cathode materials, anode materials and solid-state inorganic electrolytes. The studies on constructions of the thin film lithium batteries are also presented

Controlling Reversible Expansion of Li2O2 Formation and Decomposition by Modifying Electrolyte in Li-O2 Batteries

锂空电池分别使用空气中的氧气和金属锂作为正负极活性材料，具有极高的能量密度。但是，这一体系尚不能实现商业化的应用，其中一些关键问题未能解决。由于其正极活性材料是气体，使得电化学反应涉及气-液-固三相界面，电极过程十分复杂。与其它二次电池相比，空气电极需要考虑结构因素和催化因素。不仅要改善氧气电化学反应的动力学迟缓问题，还要考虑放电产物的驻留空间问题。董全峰教授课题组在前期开展了基于空气电极固相表面电催化研究，并结合电极结构方面的问题，构筑了有利于氧气发生反应的仿生开放式结构电极。 该研究工作主要由化学化工学院2015级iChEM直博生林晓东（第一作者）在董全峰教授、郑明森副教授和龚磊副教授的共同指导下完成，理论计算由袁汝明助理教授（共同第一作者）完成，曹勇、丁晓兵、蔡森荣、韩博闻等学生参与了部分工作。周志有教授和洪宇浩博士生在电化学微分质谱方面给予大力的帮助与支持。【Abstract】The aprotic lithium-oxygen (Li-O2) battery has attracted worldwide attention because of its ultrahigh theoretical energy density. However, its practical application is critically hindered by cathode passivation, large polarization, and severe parasitic reactions. Here, we demonstrate an originally designed Ru(Ⅱ) polypyridyl complex (RuPC) though which the reversible expansion of Li2O2 formation and decomposition can be achieved in Li-O2 batteries. Experimental and theoretical results revealed that the RuPC can not only expand the formation of Li2O2 in electrolyte but also suppress the reactivity of LiO2 intermediate during discharge, thus alleviating the cathode passivation and parasitic reactions significantly. In addition, an initial delithiation pathway can be achieved when charging in turn; thus, the Li2O2 products can be decomposed reversibly with a low overpotential. Consequently, the RuPC-catalyzed Li-O2 batteries exhibited a high discharge capacity, a low charge overpotential, and an ultralong cycle life. This work provides an alternative way of designing the soluble organic catalysts for metal-O2 batteries.This work was supported by the National 973 Program (2015CB251102), the Key Project of National Natural Science Foundation of China (21673196, 21621091, 21703186, 21773192),and the Fundamental Research Funds for the Central Universities (20720150042,20720150043). The authors thank Prof. Eric Meggers at Philipps-Univeristaet Marburg for his discussion about the synthesis of RuPC complex; Prof. Gang Fu at Xiamen University for his instructive discussions in DFT calculations; Lajia Yu and Dandan Tao at Xiamen University for their assistance in EPR experiments and UV-Vis spectroscopy experiments, respectively; and Yu Gu and Tao Wang at Xiamen University for their discussions in XPS results and CV data,respectively. 该工作得到科技部重大基础研究计划（项目批准号：2015CB251102）、国家自然科学基金（项目批准号：21673196、21621091、21703186、21773192）和中央高校基本科研业务费专项资金（项目批准号：20720150042、20720150043）的资助。 此外，感谢傅钢教授在理论计算方面的讨论和建议，Eric Meggers教授在配合物合成上的讨论，泉州师范学院吴启辉教授和化学化工学院谷宇博士生在X射线光电子能谱方面的帮助，于腊佳老师在电子顺磁共振实验上的帮助，陶丹丹博士生在紫外可见光谱测试上的帮助以及王韬博士生在循环伏安方面的讨论

Two-and three-electrode impedance spectroscopic studies of graphite electrode in the first lithiation

The first lithiation of graphite electrode was investigated by electrochemical impedance spectroscopy (EIS) and scanning electron microscope (SEM) in a two-electrode button cell and a three-electrode glass cell. The results demonstrate that the study of the variation of EIS feature of the graphite electrode in the two-electrode button cell with electrode polarization potential decreasing in the first lithiation cannot be used to investigate the formation mechanism of the solid electrolyte interphase (SEI) film. However, the formation and growth process of the SEI film can be acquired by investigating the variation of EIS features of the graphite electrode in the three-electrode glass cell with the decrease of electrode polarization potential in the first lithiation. Moreover, the results also point out that the SEI film on graphite electrode is mainly formed between 1.0 and 0.6 V in the first lithiation.Major State Basic Research Development Program of China [2009CB220102

An electrochemical impedance spectroscopic study of the electronic and ionic transport properties of LiCoO2 cathode

The storage behavior and process of the first delithiation-lithiation of LiCoO2 cathode were investigated by electrochemical impedance spectroscopy (EIS). The electronic and ionic transport properties of LiCoO2 cathode along with variation of electrode potential were obtained in 1 mol.L-1 LiPF6-EC: DMC: DEC electrolyte solution. It was found that after 9 h storage of the LiCoO2 cathode in electrolyte solutions, a new arc appears in the medium frequency range in Nyquist plots of EIS, which increases with increasing the storage time. In the charge/discharge processes, the diameter of the new arc is reversibly changed with electrode potential. Such variation coincides well with the electrode potential dependence of electronic conductivity of the LiCoO2.. Thus this new EIS feature is attributed to the change of electronic conductivity of LixCoO2 during storage of the LiCoO2 cathode in electrolyte solutions, as well as in processes of intercalation-deintercalationtion of lithium ions. It has been revealed that the reversible increase and decrease of the resistance of SEI film in charge-discharge processes can be also ascribed to the variation of electronic conductance of active materials of the LiCoO2 cathode