Decheng Li
Soochow University (Taiwan)
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Featured researches published by Decheng Li.
RSC Advances | 2013
Weiwei Liu; Guoqing Fang; Bingbo Xia; Hongdan Sun; Shingo Kaneko; Decheng Li
To improve the rate capability of lithium-rich layered cathode material Li[Li0.2Ni0.17Mn0.56Co0.07]O2 a facile method aimed at micro-structural rearrangement was proposed. Through the combination of excess lithium and chemical activation post-treatment, the resulting material showed well ordered bulk and surface structures. The capacity retention for the modified material improved significantly (compared with untreated sample) at high discharge current densities. Moreover, the unique electrochemical behavior of the modified material reveals the existence of the chemically activated Li2MnO3 component within the composite.
Journal of Solid State Electrochemistry | 2013
Guoqing Fang; Weiwei Liu; Shingo Kaneko; Bingbo Xia; Hongdan Sun; Junwei Zheng; Decheng Li
Sn-Co-C alloy as a promising anode material was prepared via a facile carbothermal reduction method, using both graphite and sucrose as the composited carbon sources. The effect of the combination pattern of graphite and sucrose on the microstructure and electrochemical performances of the alloys was investigated using X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and galvanostatic cycling tests. Compared with the Sn-Co-C samples using only graphite or sucrose as the carbon sources, the sample using the composited carbon sources has a relative higher reversible capacity and better rate capability, which is probably related to the continuous and stable conductive network formed by graphite and amorphous carbon originated from the thermal decomposition of sucrose, as well as the small particle size and uniform distribution in the conductive network.
Chemical Research in Chinese Universities | 2013
Shici He; Qian Zhang; Weiwei Liu; Guoqing Fang; Yuichi Sato; Junwei Zheng; Decheng Li
LiNi0.5Mn1.5O4 prepared by a spray drying method was re-treated in N2 at 500, 600 and 700 °C, respectively. Their structural and electrochemical properties were studied by means of Fourier transform infrared(FTIR), X-ray diffraction(XRD), and charge-discharge tests. The space group of the LiNi0.5Mn1.5O4 transforms from P4332 to
RSC Advances | 2018
Xianyu Zhu; Jingbin Quan; Jichun Huang; Zheng Ma; Yixin Chen; Decheng Zhu; Chongxing Ji; Decheng Li
Electrochimica Acta | 2011
Bing Liu; Qian Zhang; Shici He; Yuichi Sato; Junwei Zheng; Decheng Li
Fd\bar 3m
Electrochimica Acta | 2013
Guoqing Fang; Shingo Kaneko; Weiwei Liu; Bingbo Xia; Hongdan Sun; Ruixue Zhang; Junwei Zheng; Decheng Li
Archive | 2012
Bing Liu; Shici He; Xi Zhang; Junwei Zheng; Decheng Li
at an annealing temperature of 700 °C. The electrochemical characteristics of the treated samples are closely related to the annealing temperature. The sample treated in N2 at 500 °C shows both an improved rate capability and cyclic performance at a high temperature compared with the as-prepared sample, while the sample treated in N2 at 700 °C shows dramatically decrease in its reversible capacity.
Archive | 2012
Decheng Li; Shici He; Xi Zhang; Weiwei Liu; Guoqing Fang; Hongdan Sun; Bingbo Xia; Junwei Zheng
ZnMn2O4 and Zn1−xAlxMn2O4 were synthesized by a spray drying process followed by an annealing treatment. Their structural and electrochemical characteristics were investigated by SEM, XRD, XPS, charge–discharge tests and EIS. XPS data indicate that the substitution of Al3+ for Zn2+ causes manganese to be in a mixed valence state by a charge compensation mechanism. Moreover, the presence of this charge compensation significantly improves the electrochemical performance of Zn1−xAlxMn2O4, such as increasing the initial coulombic efficiency, stabilizing the cycleability as well as improving the rate capability. The sample with 2% Al doping shows the best performance, with a first cycle coulombic efficiency of 69.6% and a reversible capacity of 597.7 mA h g−1 after 100 cycles. Even at the high current density of 1600 mA g−1, it still retained a capacity of 558 mA h g−1.
Archive | 2012
Shici He; Bing Liu; Qian Zhang; Kunlin Ru; Junwei Zheng; Decheng Li
Electrochimica Acta | 2011
Bing Liu; Qian Zhang; Shici He; Yuichi Sato; Junwei Zheng; Decheng Li