Although electrically conductive and hydrophilic MXene sheets are promising for multifunctional fibers and electronic textiles,it is still a challenge to simultaneously enhance both conductivity and mechanical propert...Although electrically conductive and hydrophilic MXene sheets are promising for multifunctional fibers and electronic textiles,it is still a challenge to simultaneously enhance both conductivity and mechanical properties of MXene fibers because of the high rigidity of MXene sheets and insufficient inter-sheet interactions.Herein,we demonstrate a core-shell wet-spinning methodology for fabricating highly conductive,super-tough,ultra-strong,and environmentally stable Ti_(3)C_(2)T_(x) MXene-based core-shell fibers with conductive MXene cores and tough aramid nanofiber(ANF)shells.The highly orientated and low-defect structure endows the ANF@MXene core-shell fiber with supertoughness of~48.1 MJ m^(-3),high strength of~502.9 MPa,and high conductivity of~3.0×10^(5)S m^(-1).The super-tough and conductive ANF@MXene fibers can be woven into textiles,exhibiting an excellent electromagnetic interference(EMI)shielding efficiency of 83.4 dB at a small thickness of 213μm.Importantly,the protection of the ANF shells provides the fibers with satisfactory cyclic stability under dynamic stretching and bending,and excellent resistance to acid,alkali,seawater,cryogenic and high temperatures,and fire.The oxidation resistance of the fibers is demonstrated by their wellmaintained EMI shielding performances.The multifunctional core-shell fibers would be highly promising in the fields of EMI shielding textiles,wearable electronics and aerospace.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 the fields of electronic skin and soft wearable sensors,intrinsically stretchable conductors undergo rapid development;however,practical applications of artificial skinlike materials/devices have not been realized ...In the fields of electronic skin and soft wearable sensors,intrinsically stretchable conductors undergo rapid development;however,practical applications of artificial skinlike materials/devices have not been realized because of the difficulty in combining the electromechanical properties and sensing performance.Contrarily,insoluble inorganic conductive domains in the hydrogel matrix are generally incompatible with surrounding elastic networks,decreasing the mechanical strength.Usually,the hydrogels are vulnerable either to severe mechanical stimuli or large deformation,especially when notches are induced.In this study,based on an energy-dissipative dual-crosslinked conductive hydrogel,a mechanically durable and super-tough strain sensor was developed.The highly soft yet dynamically tough hydrogel demonstrated high ionic conductivity(30.2 mS cm^(-1)),ultrastretchability(>600%strain),and superior linear dependence of strain sensitivity with a maximum gauge factor of 1.2 at 500%strain.Because of these advantageous synergistic effects,the resultant hydrogel strain sensor demonstrated reliable and stable detection of a large range of human motion and subtle vibrations.Moreover,it impressively exhibited super toughness that could endure consecutive treading pressure and even retain normal operation after 20 times of car run-over on the road.These demonstrations highly confirm the sensor’s superior mechanical durability and reliability,displaying great potential in developing next-generation mechanically adaptable sensors.展开更多
Nanocomposite fibers have attracted intensive attentions owing to their promising applications in various fields. However, the fabrication of nanocomposite fibers with super toughness and strong strength under mild co...Nanocomposite fibers have attracted intensive attentions owing to their promising applications in various fields. However, the fabrication of nanocomposite fibers with super toughness and strong strength under mild conditions remains a great challenge. Here we present a facile flow-induced assembly strategy for the development of super-tough and strong nanocomposite fibers with highly ordered carbon nanotubes (CNTs), which can be induced by directional and fast flow on a grooved hydrogel surface. The prepared nanocomposite fibers show excellent mechanical properties, with a tensile strength up to 643±27 MPa and toughness as high as 77.3±3.4 MJ m^-3 at ultimate strain of 14.8±1.5%. This versatile and efficient flow-induced alignment strategy represents a promising direction for the development of high-performance nanocomposites for practical applications.展开更多
Multi-bond network(MBN) hydrogels contain hierarchical dynamic bonds with different bond association energy as energy dissipation units,enabling super-tough mechanical properties.In this work,we copolymerize a protona...Multi-bond network(MBN) hydrogels contain hierarchical dynamic bonds with different bond association energy as energy dissipation units,enabling super-tough mechanical properties.In this work,we copolymerize a protonated 2-ureido-4[1 H]-pyrimidone(UPy)-contained monomer with acrylic acid in HCl solution.After removing excess HCl,UPy motifs are deprotonated and from dimers,thus generating an UPy-contained MBN hydrogel.The obtained MBN hydrogels(75 wt% watercontent) exhibit super-tough mechanical properties(0.39 MPa to 2.51 MPa tensile strength),with tremendous amount of energy(1.68 MJ/m^(3) to 11.1 MJ/m^(3)) dissipated by the dissociation of UPy dimers.The introduction of ionic bonds can further improve the mechanical properties.Moreover,owing to their dynamic nature,both UPy dimers and ionic bonds can re-associate after being dissociated,resulting in excellent self-recovery ability(around 90% recovery efficiency within only 1 h).The excellent self-recovery ability mainly originates from the re-association of UPy dimers based on the high dimerization constant of UPy motifs.展开更多
Hydrogel-based quasi-solid-state electrolytes(Q-SSEs) swollen with electrolyte solutions are important components in stretchable supercapacitors and other wearable devices. This work fabricates a supertough, fatigue-r...Hydrogel-based quasi-solid-state electrolytes(Q-SSEs) swollen with electrolyte solutions are important components in stretchable supercapacitors and other wearable devices. This work fabricates a supertough, fatigue-resistant, and alkali-resistant multi-bond network(MBN) hydrogel aiming to be an alkaline Q-SSE. To synthesize the hydrogel, a 2-ureido-4[1H]-pyrimidone(UPy) motif is introduced into a poly(acrylic acid) polymer chain. The obtained MBN hydrogels with 75 wt% water content exhibit tensile strength as high as 2.47 MPa, which is enabled by the large energy dissipation ability originated from the dissociation of UPy dimers due to their high bond association energy. Owing to the high dimerization constant of UPy motifs, the dissociated UPy motifs are able to partially re-associate soon after being released from external forces, resulting in excellent fatigue-resistance. More importantly, the MBN hydrogels exhibit excellent alkali-resistance ability. The UPy Gel-10 swollen with 1 mol/L KOH display a tensile strength as high as ~1.0 MPa with elongation at break of ~550%. At the same time, they show ionic conductivity of ~17 m S/cm, which do not decline even when the hydrogels are stretched to 500% strain.The excellent mechanical property and ionic conductivity of the present hydrogels demonstrate potential application as a stretchable alkaline Q-SSE.展开更多
基金Financial support from the National Natural Science Foundation of China(51922020,52090034)the Fundamental Research Funds for the Central Universities(BHYC1707B,XK1802-2)。
文摘Although electrically conductive and hydrophilic MXene sheets are promising for multifunctional fibers and electronic textiles,it is still a challenge to simultaneously enhance both conductivity and mechanical properties of MXene fibers because of the high rigidity of MXene sheets and insufficient inter-sheet interactions.Herein,we demonstrate a core-shell wet-spinning methodology for fabricating highly conductive,super-tough,ultra-strong,and environmentally stable Ti_(3)C_(2)T_(x) MXene-based core-shell fibers with conductive MXene cores and tough aramid nanofiber(ANF)shells.The highly orientated and low-defect structure endows the ANF@MXene core-shell fiber with supertoughness of~48.1 MJ m^(-3),high strength of~502.9 MPa,and high conductivity of~3.0×10^(5)S m^(-1).The super-tough and conductive ANF@MXene fibers can be woven into textiles,exhibiting an excellent electromagnetic interference(EMI)shielding efficiency of 83.4 dB at a small thickness of 213μm.Importantly,the protection of the ANF shells provides the fibers with satisfactory cyclic stability under dynamic stretching and bending,and excellent resistance to acid,alkali,seawater,cryogenic and high temperatures,and fire.The oxidation resistance of the fibers is demonstrated by their wellmaintained EMI shielding performances.The multifunctional core-shell fibers would be highly promising in the fields of EMI shielding textiles,wearable electronics and aerospace.
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the Science Technology and Innovation Committee of Shenzhen Municipality under Shenzhen Technology Project(JSGG20180508151728414)the Department of Science and Technology of Guangdong Province under Guangdong Science and Technology Project(2018B020208001)。
文摘In the fields of electronic skin and soft wearable sensors,intrinsically stretchable conductors undergo rapid development;however,practical applications of artificial skinlike materials/devices have not been realized because of the difficulty in combining the electromechanical properties and sensing performance.Contrarily,insoluble inorganic conductive domains in the hydrogel matrix are generally incompatible with surrounding elastic networks,decreasing the mechanical strength.Usually,the hydrogels are vulnerable either to severe mechanical stimuli or large deformation,especially when notches are induced.In this study,based on an energy-dissipative dual-crosslinked conductive hydrogel,a mechanically durable and super-tough strain sensor was developed.The highly soft yet dynamically tough hydrogel demonstrated high ionic conductivity(30.2 mS cm^(-1)),ultrastretchability(>600%strain),and superior linear dependence of strain sensitivity with a maximum gauge factor of 1.2 at 500%strain.Because of these advantageous synergistic effects,the resultant hydrogel strain sensor demonstrated reliable and stable detection of a large range of human motion and subtle vibrations.Moreover,it impressively exhibited super toughness that could endure consecutive treading pressure and even retain normal operation after 20 times of car run-over on the road.These demonstrations highly confirm the sensor’s superior mechanical durability and reliability,displaying great potential in developing next-generation mechanically adaptable sensors.
基金supported by the National Key R&D Program of China(2017YFA0207800)the National Natural Science Foundation of China(21574004)+4 种基金the National Natural Science Funds for Distinguished Young Scholar(21725401)the 111 project(B14009)the Fundamental Research Funds for the Central Universitiesthe National “Young Thousand Talents Program”the China Postdoctoral Science Foundation(2017M620012)
文摘Nanocomposite fibers have attracted intensive attentions owing to their promising applications in various fields. However, the fabrication of nanocomposite fibers with super toughness and strong strength under mild conditions remains a great challenge. Here we present a facile flow-induced assembly strategy for the development of super-tough and strong nanocomposite fibers with highly ordered carbon nanotubes (CNTs), which can be induced by directional and fast flow on a grooved hydrogel surface. The prepared nanocomposite fibers show excellent mechanical properties, with a tensile strength up to 643±27 MPa and toughness as high as 77.3±3.4 MJ m^-3 at ultimate strain of 14.8±1.5%. This versatile and efficient flow-induced alignment strategy represents a promising direction for the development of high-performance nanocomposites for practical applications.
基金the National Natural Science Foundation of China(Nos.21774069,51633003 and 21474058)for financial support。
文摘Multi-bond network(MBN) hydrogels contain hierarchical dynamic bonds with different bond association energy as energy dissipation units,enabling super-tough mechanical properties.In this work,we copolymerize a protonated 2-ureido-4[1 H]-pyrimidone(UPy)-contained monomer with acrylic acid in HCl solution.After removing excess HCl,UPy motifs are deprotonated and from dimers,thus generating an UPy-contained MBN hydrogel.The obtained MBN hydrogels(75 wt% watercontent) exhibit super-tough mechanical properties(0.39 MPa to 2.51 MPa tensile strength),with tremendous amount of energy(1.68 MJ/m^(3) to 11.1 MJ/m^(3)) dissipated by the dissociation of UPy dimers.The introduction of ionic bonds can further improve the mechanical properties.Moreover,owing to their dynamic nature,both UPy dimers and ionic bonds can re-associate after being dissociated,resulting in excellent self-recovery ability(around 90% recovery efficiency within only 1 h).The excellent self-recovery ability mainly originates from the re-association of UPy dimers based on the high dimerization constant of UPy motifs.
基金the National Natural Science Foundation of China (Nos. 21774069, 51633003 and 21474058) for financial support。
文摘Hydrogel-based quasi-solid-state electrolytes(Q-SSEs) swollen with electrolyte solutions are important components in stretchable supercapacitors and other wearable devices. This work fabricates a supertough, fatigue-resistant, and alkali-resistant multi-bond network(MBN) hydrogel aiming to be an alkaline Q-SSE. To synthesize the hydrogel, a 2-ureido-4[1H]-pyrimidone(UPy) motif is introduced into a poly(acrylic acid) polymer chain. The obtained MBN hydrogels with 75 wt% water content exhibit tensile strength as high as 2.47 MPa, which is enabled by the large energy dissipation ability originated from the dissociation of UPy dimers due to their high bond association energy. Owing to the high dimerization constant of UPy motifs, the dissociated UPy motifs are able to partially re-associate soon after being released from external forces, resulting in excellent fatigue-resistance. More importantly, the MBN hydrogels exhibit excellent alkali-resistance ability. The UPy Gel-10 swollen with 1 mol/L KOH display a tensile strength as high as ~1.0 MPa with elongation at break of ~550%. At the same time, they show ionic conductivity of ~17 m S/cm, which do not decline even when the hydrogels are stretched to 500% strain.The excellent mechanical property and ionic conductivity of the present hydrogels demonstrate potential application as a stretchable alkaline Q-SSE.