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多界面耦合空心核壳MnCoSe_(x)/MnO@氮掺杂碳复合材料的制备及电化学性能
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作者 周济 张丽娜 +2 位作者 刘彬彬 徐彩霞 刘宏 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2023年第8期2471-2482,共12页
通过简单的溶剂热和硒化策略以及进一步的碳层包覆程序制备氮掺杂碳壳包裹的空心MnCoSe_(x)/MnO纳米球(MnCoSe_(x)/MnO@N-C)。得益于MnCoSe_(x)和MnO之间的多界面耦合以及独特的空心核壳结构,MnCoSe_(x)/MnO@N-C复合材料具有较高的比电... 通过简单的溶剂热和硒化策略以及进一步的碳层包覆程序制备氮掺杂碳壳包裹的空心MnCoSe_(x)/MnO纳米球(MnCoSe_(x)/MnO@N-C)。得益于MnCoSe_(x)和MnO之间的多界面耦合以及独特的空心核壳结构,MnCoSe_(x)/MnO@N-C复合材料具有较高的比电容和优异的倍率性能,即使在5 A/g的高电流密度下,MnCoSe_(x)/MnO@N-C仍可以稳定运行20000次循环,并保持84.6%的初始比电容。由MnCoSe_(x)/MnO@N-C和活性炭组装的非对称超级电容器器件在功率密度为810 W/kg时表现出11.2 W·h/kg的高能量密度,并拥有超长的循环寿命,在20000次循环后仍可保留初始比电容的84.0%。 展开更多
关键词 硒化物 空心纳米球 氮掺杂碳 正极 超级电容器 电化学性能
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One-step construction of strongly coupled Co_(3)V_(2)O_(8)/Co_(3)O_(4)/MXene heterostructure via in-situ Co-F bonds for high performance all-solid-state asymmetric supercapacitors
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作者 Ji Zhou Bin-Bin Liu +3 位作者 Hu Zheng Wen-Qing Ma Qian Li cai-xia xu 《Rare Metals》 SCIE EI CAS CSCD 2024年第2期682-691,共10页
Co_(3)V_(2)O_(8)/Co_(3)O_(4)/Ti_(3)C_(2)T_(x) composite was easily synthesized via one-step succinct-operated hydrothermal process.The interconnected Co_(3)V_(2)O_(8)/Co_(3)O_(4) nanowires network can in-situ grow and... Co_(3)V_(2)O_(8)/Co_(3)O_(4)/Ti_(3)C_(2)T_(x) composite was easily synthesized via one-step succinct-operated hydrothermal process.The interconnected Co_(3)V_(2)O_(8)/Co_(3)O_(4) nanowires network can in-situ grow and anchor on the surface of Ti_(3)C_(2)T_(x) via the strong Co-F bonds and contribute tremendously to depress Ti_(3)C_(2)T_(x) self-restacking.Profiting from the synergistically interplayed effect among the multiple interfaces and high conductivity of Ti_(3)C_(2)T_(x) as well as outstanding stability of the as-designed nanostructure,the optimum Co_(3)V_(2)O_(8)/Co_(3)O_(4)/Ti_(3)C_(2)T_(x)electrode reaches a commendable specific capacitance(up to 3800 mF·cm^(−2)),great rate capability(80%capacitance retention after 20-times current increasing),and preeminent cycling stability(95.4%/85.5%retention at 7000th/20,000th cycle).Moreover,the all-solid-state asymmetric supercapacitor based on Co_(3)V_(2)O_(8)/Co_(3)O_(4)/Ti_(3)C_(2)T_(x) and active carbon can deliver a high energy density of 84.0μWh·cm^(−2) at the power energy of 3.2 mW·cm^(−2),and excellent cycling durability with 87.0%of initial capacitance retention upon 20,000 loops.This work provides a practicable pathway to tailor MXene-based composites for high-performance supercapacitor. 展开更多
关键词 Ti_(3)C_(2)T_(x) Co_(3)V_(2)O_(8)/Co_(3)O_(4) HETEROSTRUCTURE Cathode Supercapacitor
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Carbon shell coated hollow NiCoSe_(x)composite as high-performance anode for lithium storage 被引量:7
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作者 Zi-Zhong Chen Jia-Gang Hou +3 位作者 Ji Zhou Peng Huang Hai-Qing Wang cai-xia xu 《Rare Metals》 SCIE EI CAS CSCD 2021年第11期3185-3194,共10页
Hollow NiCoSe_(x)(H-NiCoSe_(x)) nanospheres encapsulated with carbon shell were prepared via one-step easy solvothermal method followed by the carbon coating process.H-NiCoSe_(x)@C has large interior void with the uni... Hollow NiCoSe_(x)(H-NiCoSe_(x)) nanospheres encapsulated with carbon shell were prepared via one-step easy solvothermal method followed by the carbon coating process.H-NiCoSe_(x)@C has large interior void with the uniform dimension around 350 nm and the thickness of carbon shell around 20-30 nm.Coupling with the large interior void as well as robust protective carbon shell,H-NiCoSe_(x)@C can retain the reversible capacity of 805.6 mAh·g^(-1) after 100 cycles at 200 mA·g^(-1).In particular,H-NiCoSe_(x)@C delivers large reversible capacity of 1532.2 mAh·g^(-1) upon cycling for 1000 loops at 1000 mA·g^(-1)with the capacity retention as high as 128.2% upon long period of activation.Even at the high rate of 3000 mA·g^(-1),its specific capacity still retains up to 659.3 mAh·g^(-1).The superior lithium storage performances for H-NiCoSe_(x)@C profit from its robust hollow core-shell structure as well as enhanced electrical conductivity and ion transport. 展开更多
关键词 SELENIDE Hollow sphere Carbon shell Lithium-ion batteries ANODE
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Catalyst-free hydrochlorination protocol for terminal arylalkynes with hydrogen chloride
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作者 cai-xia xu Cun-Hua Ma +2 位作者 Fu-Rong Xiao Hong-Wei Chen Bin Dai 《Chinese Chemical Letters》 SCIE CAS CSCD 2016年第11期1683-1685,共3页
We present a simple and straightforward protocol for hydrochlorination of terminal arylalkynes to vinyl chlorides using hydrogen chloride under mild reaction conditions. This protocol does not involve any metal cataly... We present a simple and straightforward protocol for hydrochlorination of terminal arylalkynes to vinyl chlorides using hydrogen chloride under mild reaction conditions. This protocol does not involve any metal catalysts or additives. It is simple, inexpensive, and easy to prepare, and exhibits good reaction activity. The hydrochlorination proceeds smoothly to yield unique regioselective products via the Markovnikov addition rule. 展开更多
关键词 Hydrochlorination Arylalkynes Vinyl chlorides Catalyst-free Markovnikov addition
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