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锂离子电池能量效率的研究 被引量:6
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作者 高红 吕丰 +1 位作者 魏学哲 戴海峰 《电源技术》 CAS CSCD 北大核心 2013年第12期2132-2134,2228,共4页
现有能量效率算法只能反映充放电一个循环的效率,它将充电能量损失与放电能量损失耦合在一起,不适用于充电和放电过程分离的场合。基于锂离子电池OCV与SOC之间存在一一对应关系,提出了电池理论能量的概念,将电池的能量效率细分为充电能... 现有能量效率算法只能反映充放电一个循环的效率,它将充电能量损失与放电能量损失耦合在一起,不适用于充电和放电过程分离的场合。基于锂离子电池OCV与SOC之间存在一一对应关系,提出了电池理论能量的概念,将电池的能量效率细分为充电能量效率、放电能量效率以及充放电能量效率,提出了适用于这类电池的能量效率算法,并通过实验验证了该算法的可行性。 展开更多
关键词 电池理论能量 充电能量效率 放电能量效率 充放电能量效率 锂离子电池
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Multifunctional V3S4-nanowire/graphene composites for high performance Li-S batteries 被引量:6
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作者 Tianyu Tang Teng Zhang +7 位作者 Lina Zhao Biao Zhang Wei Li Junjie Xu Tao Li Long Zhang Hailong Qiu Yanglong Hou 《Science China Materials》 SCIE EI CSCD 2020年第10期1910-1919,共10页
Lithium sulfur(Li-S)batteries have been regarded as a promising next-generation energy storage system with high theoretical specific capacity and energy density,but still facing challenges.In order to make Li-S batter... Lithium sulfur(Li-S)batteries have been regarded as a promising next-generation energy storage system with high theoretical specific capacity and energy density,but still facing challenges.In order to make Li-S batteries more competitive,combination of trapping sites and electrocatalytic properties for polysulfides is an effective way to improve the battery performance.In this study,we prepare a type of multifunctional V3S4-nanowire/graphene composites(V3S4-G)by uniformly dispersing V3S4 nanowires on the graphene substrate.This structure contributes to the sufficient exposure of multifunctional V3S4 active sites which can anchor polysulfides and accelerate reaction kinetics.Thus,the Li-S batteries based on the multifunctional V3S4-G sulfur cathode deliver a stable cycling performance and good rate capability.Even at sulfur loading of 3 mg cm^−2,the V3S4-G sulfur cathode possesses a low capacity decay rate of 0.186%per cycle at 0.5 C. 展开更多
关键词 Li-S batteries V3S4-G trapping sites electrocatalytic properties
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Enhancing sodium-ion storage performance of MoO/N-doped carbon through interfacial Mo–N–C bond 被引量:1
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作者 Bin Huang Shuang Liu +7 位作者 Xu Zhao Yanwei Li Jianwen Yang Quanqi Chen Shunhua Xiao Wenhua Zhang Hong-En Wang Guozhong Cao 《Science China Materials》 SCIE EI CSCD 2021年第1期85-95,共11页
Na-ion batteries(SIBs)have attracted considerable attention as promising alternatives to commercial Li-ion batteries(LIBs)due to comparable redox potential,and natural abundance of Na.However,it remains challenging to... Na-ion batteries(SIBs)have attracted considerable attention as promising alternatives to commercial Li-ion batteries(LIBs)due to comparable redox potential,and natural abundance of Na.However,it remains challenging to explore suitable anodes for SIBs.Herein,a MoO2/N-doped carbon(MoO2/N-C)composite composed of MoO2 nanocrystals embedded within carbon matrix with a Mo–N–C chemical bond is prepared by a simple yet effective carbonization-induced topochemical transformation route.Na-ion half-cells using MoO2/N-C exhibit excellent cycling stability over 5000 cycles at 5 A g^-1 and superior rate capability.Physicochemical characterizations and first-principles density functional theory(DFT)simulations reveal that the formation of chemical bond at the interface between MoO2 and N-doped carbon plays an important role in the excellent charge storage properties of MoO2/N-C.More importantly,the interfacial coupling can efficiently promote interface charge transfer.Benefiting from this,Na-ion capacitors(SICs)constructed with the MoO2/N-C anode and activated carbon cathode can deliver an impressive energy density of 15 W h kg^-1 at a power density of 1760 W kg^-1,together with a capacitance retention of 92.4%over 1000 cycles at 10 A g^-1.The proposed strategy in this paper based on interfacial chemical bond may hold promises for the design of high-performance electrodes for energy storage devices. 展开更多
关键词 topochemical transformation Mo–N chemical bond Na-ion batteries Na-ion capacitor density functional theory simulations
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