Halide solid-state electrolytes(HSSEs)with excellent ionic conductivity and high voltage stability are promising for all-solid-state Li-ion batteries(ASSLBs).However,they suffer from poor processability,mechanical dur...Halide solid-state electrolytes(HSSEs)with excellent ionic conductivity and high voltage stability are promising for all-solid-state Li-ion batteries(ASSLBs).However,they suffer from poor processability,mechanical durability and humidity stability,hindering their large-scale applications.Here,we introduce a dry-processing fibrillation strategy using hydrophobic polytetrafluoroethylene(PTFE)binder to encapsulate Li_(3)InCl_(6)(LIC)particles(the most representative HSSE).By manipulating the fibrillating process,only 0.5 wt%PTFE is sufficient to prepare free-standing LIC-PTFE(LIC-P)HSSEs.Additionally,LIC-P demonstrates excellent mechanical durability and humidity resistance.They can maintain their shapes after being exposed to humid atmosphere for 30 min,meanwhile still exhibit high ionic conductivity of>0.2m S/cm at 25℃.Consequently,the LIC-P-based ASSLBs deliver a high specific capacity of 126.6 m Ah/g at0.1 C and long cyclability of 200 cycles at 0.2 C.More importantly,the ASSLBs using moisture-exposed LIC-P can still operate properly by exhibiting a high capacity-retention of 87.7%after 100 cycles under0.2 C.Furthermore,for the first time,we unravel the LIC interfacial morphology evolution upon cycling because the good mechanical durability enables a facile separation of LIC-P from ASSLBs after testing.展开更多
Polyamide/acrylonitrile-butadiene-styrene copolymer(PA/ABS) blends have drawn considerable attention from both academia and industry for their important applications in automotive and electronic areas. Due to poor mis...Polyamide/acrylonitrile-butadiene-styrene copolymer(PA/ABS) blends have drawn considerable attention from both academia and industry for their important applications in automotive and electronic areas. Due to poor miscibility of PA and ABS, developing an effective compatibilization strategy has been an urgent challenge to achieve prominent mechanical properties. In this study, we create a set of mechanically enhanced PA6/ABS blends using two multi-monomer melt-grafted compatibilizers, SEBSg-(MAH-co-St) and ABS-g-(MAH-co-St). The dispersed domain size is significantly decreased and meanwhile the unique "soft shell-encapsulating-hard core" structures form in the presence of compatibilizers. The optimum mechanical performances manifest an increase of 36% in tensile strength and an increase of 1300% in impact strength, compared with the neat PA6/ABS binary blend.展开更多
In this study, the maleic anhydride （MAH） and styrene （St） dual monomers grafted polypropylene （PP） and poly[styrene-b- （ethylene-co-butylene）-b-styrene] （SEBS）, i.e. PP-g-（MAH-co-St） and SEBS-g-（MAH-co-S...In this study, the maleic anhydride （MAH） and styrene （St） dual monomers grafted polypropylene （PP） and poly[styrene-b- （ethylene-co-butylene）-b-styrene] （SEBS）, i.e. PP-g-（MAH-co-St） and SEBS-g-（MAH-co-St） are prepared as multi-phase compatibilizers and used to compatibilize the PA6/PS/PP/SEBS （70/10/10/10） model quaternary blends. Both PS and SEBS are encapsulated by the hard shell of PP-g-（MAH-co-St） in the dispersed domains （about 2 μm） of the PA6/PS/PP-g-（MAH-co-St）/SEBS （70/10/10/10） quaternary blend. In contrast, inside the dispersed domains （about 1 μm） of the PA6/PS/PP/SEBS-g-（MAH-co-St） （70/10/10/10） quaternary blend, the soft SEBS-g-（MAH-co-St） encapsulates both the hard PS and PP phases and separates them. With increasing the content of the compatibilizers equally, the morphology of the PA6/PS/（PP＋PP-g-（MAH-co-St））/（SEBS＋SEBS-g-（MAH-co-St）） （70/10/10/10） quaternary blends evolves from the soft （SEBS＋SEBS-g-（MAH-co-St）） encapsulating PS and partially encapsulating PP （about 1 μm）, then to PS exclusively encapsulated by the soft SEBS-g-（MAH-co-St） and then separated by PP-g-（MAH-co-St） inside the smaller domains （about 0.6 μm）. This morphology evolution has been well predicted by spreading coefficients and explained by the reaction between the matrix PA6 and the compatibilizers. The quaternary blends compatibilized by more compatibilizers exhibit stronger hierarchical interfacial adhesions and smaller dispersed domain, which results in the further improved mechanical properties. Compared to the uncompatibilized blend, the blend with both 10 wt% PP-g-（MAH-co-St） and 10 wt% SEBS-g-（MAH-co-St） has the best mechanical properties with the stress at break, strain at break and impact failure energy improved significantly by 97%, 71% and 261%, respectively. There is a strong correlation between the structure and property in the blends.展开更多
基金supported by the 261 Project of MIITthe National Natural Science Foundation of China(Nos.52250010,52201242,U23A20574)the Young Elite Scientists Sponsorship Program by CAST(No.2021QNRC001)。
文摘Halide solid-state electrolytes(HSSEs)with excellent ionic conductivity and high voltage stability are promising for all-solid-state Li-ion batteries(ASSLBs).However,they suffer from poor processability,mechanical durability and humidity stability,hindering their large-scale applications.Here,we introduce a dry-processing fibrillation strategy using hydrophobic polytetrafluoroethylene(PTFE)binder to encapsulate Li_(3)InCl_(6)(LIC)particles(the most representative HSSE).By manipulating the fibrillating process,only 0.5 wt%PTFE is sufficient to prepare free-standing LIC-PTFE(LIC-P)HSSEs.Additionally,LIC-P demonstrates excellent mechanical durability and humidity resistance.They can maintain their shapes after being exposed to humid atmosphere for 30 min,meanwhile still exhibit high ionic conductivity of>0.2m S/cm at 25℃.Consequently,the LIC-P-based ASSLBs deliver a high specific capacity of 126.6 m Ah/g at0.1 C and long cyclability of 200 cycles at 0.2 C.More importantly,the ASSLBs using moisture-exposed LIC-P can still operate properly by exhibiting a high capacity-retention of 87.7%after 100 cycles under0.2 C.Furthermore,for the first time,we unravel the LIC interfacial morphology evolution upon cycling because the good mechanical durability enables a facile separation of LIC-P from ASSLBs after testing.
基金the National Natural Science Foundation of China (No. 51633003) for the financial support
文摘Polyamide/acrylonitrile-butadiene-styrene copolymer(PA/ABS) blends have drawn considerable attention from both academia and industry for their important applications in automotive and electronic areas. Due to poor miscibility of PA and ABS, developing an effective compatibilization strategy has been an urgent challenge to achieve prominent mechanical properties. In this study, we create a set of mechanically enhanced PA6/ABS blends using two multi-monomer melt-grafted compatibilizers, SEBSg-(MAH-co-St) and ABS-g-(MAH-co-St). The dispersed domain size is significantly decreased and meanwhile the unique "soft shell-encapsulating-hard core" structures form in the presence of compatibilizers. The optimum mechanical performances manifest an increase of 36% in tensile strength and an increase of 1300% in impact strength, compared with the neat PA6/ABS binary blend.
基金financially supported by the National Natural Science Foundation of China (No. 51633003)State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology (No. OIC-201601006)
文摘In this study, the maleic anhydride （MAH） and styrene （St） dual monomers grafted polypropylene （PP） and poly[styrene-b- （ethylene-co-butylene）-b-styrene] （SEBS）, i.e. PP-g-（MAH-co-St） and SEBS-g-（MAH-co-St） are prepared as multi-phase compatibilizers and used to compatibilize the PA6/PS/PP/SEBS （70/10/10/10） model quaternary blends. Both PS and SEBS are encapsulated by the hard shell of PP-g-（MAH-co-St） in the dispersed domains （about 2 μm） of the PA6/PS/PP-g-（MAH-co-St）/SEBS （70/10/10/10） quaternary blend. In contrast, inside the dispersed domains （about 1 μm） of the PA6/PS/PP/SEBS-g-（MAH-co-St） （70/10/10/10） quaternary blend, the soft SEBS-g-（MAH-co-St） encapsulates both the hard PS and PP phases and separates them. With increasing the content of the compatibilizers equally, the morphology of the PA6/PS/（PP＋PP-g-（MAH-co-St））/（SEBS＋SEBS-g-（MAH-co-St）） （70/10/10/10） quaternary blends evolves from the soft （SEBS＋SEBS-g-（MAH-co-St）） encapsulating PS and partially encapsulating PP （about 1 μm）, then to PS exclusively encapsulated by the soft SEBS-g-（MAH-co-St） and then separated by PP-g-（MAH-co-St） inside the smaller domains （about 0.6 μm）. This morphology evolution has been well predicted by spreading coefficients and explained by the reaction between the matrix PA6 and the compatibilizers. The quaternary blends compatibilized by more compatibilizers exhibit stronger hierarchical interfacial adhesions and smaller dispersed domain, which results in the further improved mechanical properties. Compared to the uncompatibilized blend, the blend with both 10 wt% PP-g-（MAH-co-St） and 10 wt% SEBS-g-（MAH-co-St） has the best mechanical properties with the stress at break, strain at break and impact failure energy improved significantly by 97%, 71% and 261%, respectively. There is a strong correlation between the structure and property in the blends.
