氟是废旧锂电池回收难以回避的典型杂质元素,其迁移转化行为复杂,制约了高品质正极材料的可控再生制备.本研究通过揭示废旧锂电池在热解、浸出及高镍LiNi_(0.9)Co_(0.05)Mn_(0.05)O_(2)材料再生过程中氟的迁移转化规律,为氟的定向调控...氟是废旧锂电池回收难以回避的典型杂质元素,其迁移转化行为复杂,制约了高品质正极材料的可控再生制备.本研究通过揭示废旧锂电池在热解、浸出及高镍LiNi_(0.9)Co_(0.05)Mn_(0.05)O_(2)材料再生过程中氟的迁移转化规律,为氟的定向调控及材料的可控再生制备奠定理论基础实验结果表明:热解过程中部分氟(45.71%)以气态热解产物的形式释放到大气中,而另一部分氟(52.34%)则向废三元材料的晶格内发生迁移,并随着湿法浸出溶解到镍钴锰的浸出液中.浸出液中少量的氟会在共沉淀制备前驱体过程中迁移到Ni_(0.9)Co_(0.05)Mn_(0.05)(OH)2前驱体材料,并随着配锂烧结掺杂到再生LiNi_(0.9)Co_(0.05)Mn_(0.05)O_(2)材料表面.进一步通过调控氟含量发现,当浸出液中氟浓度控制在0.30 g L^(-1)时,引入到再生LiNi_(0.9)Co_(0.05)Mn_(0.05)O_(2)材料中的氟不仅不会引起不利相变,而且能够稳定材料结构,从而有效提升再生高镍材料的循环稳定性(1 C电流密度下循环100圈的容量保持率高达95.7%).因此,本研究不仅揭示了废旧锂电池回收过程中氟的迁移转化行为,而且可控再生制备了高性能氟掺杂高镍LiNi_(0.9)Co_(0.05)Mn_(0.05)O_(2)正极材料,为废旧锂离子电池回收过程中氟的调控提供了理论依据.展开更多
The poor electrochemical performance of all-solid-state batteries(ASSBs),which is assemblied by Ni-rich cathode and poly(ethylene oxide)(PEO)-based electrolytes,can be attributed to unstable cathodic interface and poo...The poor electrochemical performance of all-solid-state batteries(ASSBs),which is assemblied by Ni-rich cathode and poly(ethylene oxide)(PEO)-based electrolytes,can be attributed to unstable cathodic interface and poor crystal structure stability of Ni-rich cathode.Several coating strategies are previously employed to enhance the stability of the cathodic interface and crystal structure for Ni-rich cathode.However,these methods can hardly achieve simplicity and high efficiency simultaneously.In this work,polyacrylic acid(PAA)replaced traditional PVDF as a binder for cathode,which can achieve a uniform PAA-Li(LixPAA(0<x≤1))coating layer on the surface of single-crystal LiNi_(0.83)Co_(0.12)Mn_(0.05)O_(2)(SC-NCM83)due to H^(+)/Li^(+)exchange reaction during the initial charging-discharging process.The formation of PAA-Li coating layer on cathode can promote interfacial Li^(+)transport and enhance the stability of the cathodic interface.Furthermore,the partially-protonated surface of SC-NCM83 casued by H^(+)/Li^(+)exchange reaction can restrict Ni ions transport to enhance the crystal structure stability.The proposed SC-NCM83-PAA exhibits superior cycling performance with a retention of 92%compared with that(57.3%)of SC-NCM83-polyvinylidene difluoride(PVDF)after 200 cycles.This work provides a practical strategy to construct high-performance cathodes for ASSBs.展开更多
基金supported by the National Natural Science Foundation of China (51904340)the Natural Science Foundation of Hunan (2021JJ2020066)+1 种基金the National Key Research and Development Program (2019YFC1907801, 2019YFC1907803 and 2019YFC1907804)the Central South University Innovation-Driven Research Programme (2023CXQD009)。
文摘氟是废旧锂电池回收难以回避的典型杂质元素,其迁移转化行为复杂,制约了高品质正极材料的可控再生制备.本研究通过揭示废旧锂电池在热解、浸出及高镍LiNi_(0.9)Co_(0.05)Mn_(0.05)O_(2)材料再生过程中氟的迁移转化规律,为氟的定向调控及材料的可控再生制备奠定理论基础实验结果表明:热解过程中部分氟(45.71%)以气态热解产物的形式释放到大气中,而另一部分氟(52.34%)则向废三元材料的晶格内发生迁移,并随着湿法浸出溶解到镍钴锰的浸出液中.浸出液中少量的氟会在共沉淀制备前驱体过程中迁移到Ni_(0.9)Co_(0.05)Mn_(0.05)(OH)2前驱体材料,并随着配锂烧结掺杂到再生LiNi_(0.9)Co_(0.05)Mn_(0.05)O_(2)材料表面.进一步通过调控氟含量发现,当浸出液中氟浓度控制在0.30 g L^(-1)时,引入到再生LiNi_(0.9)Co_(0.05)Mn_(0.05)O_(2)材料中的氟不仅不会引起不利相变,而且能够稳定材料结构,从而有效提升再生高镍材料的循环稳定性(1 C电流密度下循环100圈的容量保持率高达95.7%).因此,本研究不仅揭示了废旧锂电池回收过程中氟的迁移转化行为,而且可控再生制备了高性能氟掺杂高镍LiNi_(0.9)Co_(0.05)Mn_(0.05)O_(2)正极材料,为废旧锂离子电池回收过程中氟的调控提供了理论依据.
基金the financial support from the National Natural Science Foundation of China(Nos.52034011 and 52204328)the Science and Technology Innovation Program of Hunan Province(2023RC305)the Changsha Municipal Natural Science Foundation(kq2202085)。
文摘The poor electrochemical performance of all-solid-state batteries(ASSBs),which is assemblied by Ni-rich cathode and poly(ethylene oxide)(PEO)-based electrolytes,can be attributed to unstable cathodic interface and poor crystal structure stability of Ni-rich cathode.Several coating strategies are previously employed to enhance the stability of the cathodic interface and crystal structure for Ni-rich cathode.However,these methods can hardly achieve simplicity and high efficiency simultaneously.In this work,polyacrylic acid(PAA)replaced traditional PVDF as a binder for cathode,which can achieve a uniform PAA-Li(LixPAA(0<x≤1))coating layer on the surface of single-crystal LiNi_(0.83)Co_(0.12)Mn_(0.05)O_(2)(SC-NCM83)due to H^(+)/Li^(+)exchange reaction during the initial charging-discharging process.The formation of PAA-Li coating layer on cathode can promote interfacial Li^(+)transport and enhance the stability of the cathodic interface.Furthermore,the partially-protonated surface of SC-NCM83 casued by H^(+)/Li^(+)exchange reaction can restrict Ni ions transport to enhance the crystal structure stability.The proposed SC-NCM83-PAA exhibits superior cycling performance with a retention of 92%compared with that(57.3%)of SC-NCM83-polyvinylidene difluoride(PVDF)after 200 cycles.This work provides a practical strategy to construct high-performance cathodes for ASSBs.
