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无机材料学报 | 2014

Co掺杂改性尖晶石型Li 1.035 Mn 1.965 O 4 的合成及其电化学性能

Li Yunjiao; Xu Hu; Kong Long; Li Huacheng; Li Chun-Xia; Zhang Xian-Zhen; Han Qiang

Spinel powders of Li1.035CoxMn1.965-xO4 (x=0-0.100) systems were synthesized by a simple wet chemical process with post heat-treatment. X-ray diffraction patterns (XRD) reveal that the Co doping does not affect the Fd3m space group of the cathode materials. Scanning electron microscope (SEM) images show that the Li1.035CoxMn1.965-xO4 cathode materials have a uniform and nearly cubic morphology with a narrow size distribution. Transmission electron microscope (TEM) results demonstrate that the Li1.035Co0.035Mn1.930O4 powder has a good crystalline state. The electrochemical testing results indicate that the prepared Co-doped Li1.035CoxMn1.965-xO4 samples show a better cycling ability and rate capability at room temperature than that of Co-free Li1.035Mn1.965O4. In particular, the Li1.035 Co0.035Mn1.930O4 sample delivers a reversible specific capacity of 113 mAh/g in 1 st cycle and retains 93.8% of its initial capacity after 100 cycles at 0.5C rate. When discharging at 4C rate, the Li1.035Co0.035Mn1.930O4 powder maintains 86 mAh/g, which is 76.1% of the reversible capacity at 0.5C. Comparatively, the Li1.035Mn1.965O4 powder maintains only 64.8% of its reversible capacity at 0.5C discharge rate. The electrochemical impedance spectroscopy results show that Co ion doping can enhance the electrical conductivity and the Li-ion diffusion coefficient. These results indicate a superior cycling and rate performance compared with the pristine one.采用湿化学–后续热处理技术, 合成了掺钴尖晶石锰酸锂材料。X射线衍射(XRD)分析结果表明, 钴的掺入没有改变材料的Fd3m结构。扫描电子显微镜(SEM)分析表明, 所合成的材料颗粒均匀, 形貌规整, 粒径分布较窄。透射电子显微镜(TEM)结果表明, Li 1.035 Co 0.035 Mn 1.930 O 4 具有完好的结晶态。充放电测试结果表明, 在室温下钴掺杂能够提高材料的电性能。当产物为Li 1.035 Co 0.035 Mn 1.930 O 4 时, 其电性能达到最优: 以0.5 C 充放电,首次放电容量为113 mAh/g, 经过100次循环后容量保持率为93.8%, 经过4 C 放电后仍然能够保持0.5 C 放电容量的76.1%; 而未掺钴的Li 1.035 Mn 1.965 O 4 经过4C放电容量仅保持0.5 C 放电容量的64.8%。电化学阻抗测试结果表明, 钴离子的掺杂能够提高锰酸锂材料的锂离子扩散速率。采用湿化学–后续热处理技术, 合成了掺钴尖晶石锰酸锂材料。X射线衍射(XRD)分析结果表明, 钴的掺入没有改变材料的Fd3m结构。扫描电子显微镜(SEM)分析表明, 所合成的材料颗粒均匀, 形貌规整, 粒径分布较窄。透射电子显微镜(TEM)结果表明, Li 1.035 Co 0.035 Mn 1.930 O 4 具有完好的结晶态。充放电测试结果表明, 在室温下钴掺杂能够提高材料的电性能。当产物为Li 1.035 Co 0.035 Mn 1.930 O 4 时, 其电性能达到最优: 以0.5 C 充放电,首次放电容量为113 mAh/g, 经过100次循环后容量保持率为93.8%, 经过4 C 放电后仍然能够保持0.5 C 放电容量的76.1%; 而未掺钴的Li 1.035 Mn 1.965 O 4 经过4 C 放电容量仅保持0.5 C 放电容量的64.8%。电化学阻抗测试结果表明, 钴离子的掺杂能够提高锰酸锂材料的锂离子扩散速率。


Archive | 2013

Preparation method of manganese Li-NiCoMn ternary material for lithium ion battery

Wang Chunfei; Li Huacheng; Li Puliang; Li Yunjiao; Hu Mingchao; Lu Daohuan; Zhang Liyun; Wei Kang


Archive | 2014

Synthesis and Electrochemical Characterizations of Co-doped Lithium Manganese Oxide Spinel Li1.035Mn1.965O4

Li Yunjiao; Xu Hu; Kong Long; Li Huacheng; Li Chun-Xia; Zhang Xian-Zhen; Han Qiang


Archive | 2016

Preparing method for spherical LiMn1-x-yNixCoyO2 anode material

Zhong Qing; Li Yunjiao; Li Huacheng; Chen Nanxiong; Huang Guanhan; Ming Xianquan; Zhang Liyun; Zeng Wenming; Li Zhaoming


Archive | 2017

Preparation method of high-purity manganese monoxide

Li Huacheng; Li Puliang; Li Yunjiao; Xu Hu; Kong Long; Chen Nanxiong; Wang Chunfei


Materials Letters | 2017

高電圧リチウムイオン電池のための独創的な湿式化学法によるLiNi_1/3Co_1/3Mn_1/3O_2の合成と電気化学的性質【Powered by NICT】

Su Qianye; Li Yunjiao; Li Ling; Li Wei; Cao Guolin; Xue Longlong; Li Jianguo; Cao Xinlong


Ceramics International | 2017

水熱法で調製したMoドープLiNi_0 5Co_0 2Mn_0 3O_2陰極材料の合成と特性化【Powered by NICT】

Li Yunjiao; Su Qianye; Han Qiang; Li Puliang; Li Ling; Xu Chunrui; Cao Xinlong; Cao Guolin


Archive | 2016

Preparation method of oxide-cladding lithium ion battery positive material

Wang Chunfei; Yan Guanjie; Li Yunjiao; Wang Xizhi; Li Linhui; Wu Xile; Tang Yuebo; Zeng Wenming; Li Zhaoming


Archive | 2016

Preparation method of lithium ion power battery material lithium nickel manganese oxide

Wang Chunfei; Li Yunjiao; Li Huacheng; Yan Guanjie; Li Puliang; Zhang Liyun; Huang Ruihong; Li Zhaoliang; Li Chunxia


Archive | 2016

Desulphurization and denitrogenation integrated method

Li Yunjiao; Cao Xinlong; Ye Wanqi; Zhang Xianzhen; Li Jianguo

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Li Jianguo

Technical University of Berlin

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