Cross-linked polyethylene (PEX) pipes used in hot water supply are required for high mechanical strength and high creep resistance at high temperature. Especially PEX-a pipes which are made by peroxide cross-linking h...Cross-linked polyethylene (PEX) pipes used in hot water supply are required for high mechanical strength and high creep resistance at high temperature. Especially PEX-a pipes which are made by peroxide cross-linking have better performance, such as creep resistance and thermal shock resistance than the pipes made by the other cross-linking method. Because the PEX-a pipes indicate the higher cross-link degree as compared with the other PEX pipes. In this study, the PEX-a pipes which were mixed with several stabilizers were tested to evaluate the effects on cross-link degree and the oxygen induction time. And also they are evaluated with the chlorine aqueous solution by the performance of the long-term hydrostatic pressure test and the long-term hydro dynamic pressure test. As a result, it was found that the combination of antioxidants for PEX-a pipes plays an important role to prolong the oxygen induction time without inhibiting the cross-linking. From the results of the 1H pulsed NMR measurement over the melting point of polyethylene, it was found that each peroxide PEX pipe with different antioxidant combinations indicated the different proportion and crosslink density of cross-linked region, in addition, that these pipes had the effective structure of cross-linking for the hydrostatic and hydrodynamic pressure test with the chlorine aqueous solution. Therefore, it was considered to be useful results for studies of the stricture of cross-linking of polyethylene.展开更多
Polyimide(PI)is a promising electronic packaging material,but it remains challenging to obtain an all-organic PI hybrid film with decreased dielectric constant and loss without modifying the monomer.Herein,a series of...Polyimide(PI)is a promising electronic packaging material,but it remains challenging to obtain an all-organic PI hybrid film with decreased dielectric constant and loss without modifying the monomer.Herein,a series of allorganic PI hybrid films were successfully prepared by introducing the covalent organic framework(COF),which could induce the formation of the cross-linking structure in the PI matrix.Due to the synergistic effects of the COF fillers and the cross-linking structure,the PI/COF hybrid film containing 2 wt%COF exhibited the lowest dielectric constant of 2.72 and the lowest dielectric loss(tanδ)of 0.0077 at 1 MHz.It is attributed to the intrinsic low dielectric constant of COF and a large number of mesopores within the PI.Besides,the cross-linking network of PI prevents the molecular chains from stacking and improves the fraction of free volume(FFV).The molecular dynamics simulation results are well consistent with the dielectric properties data.Furthermore,the PI/COF hybrid film with 5 wt%COF showed a significant enhancement in breakdown strength,which increased to 412.8 kV/mm as compared with pure PI.In addition,the PI/COF hybrid film achieve to reduce the dielectric constant and thermal expansion coefficient(CTE).It also exhibited excellent thermal,hydrophobicity,and mechanical performance.The all-organic PI/COF hybrid films have great commercial potential as next-generation electronic packaging materials.展开更多
Large-scale and low-cost preparation of carbon-based potassium anode with long life and high capacity is one of the footstones for the development of potassium ion batteries(PIBs).Herein,a low-cost carbon-based materi...Large-scale and low-cost preparation of carbon-based potassium anode with long life and high capacity is one of the footstones for the development of potassium ion batteries(PIBs).Herein,a low-cost carbon-based material,cross-linked hollow graphitic carbon(HGC),is large scale synthesized to apply for PIBs anode.Its hollow structure can afford sufficient space to overcome the damage caused by the volume expansion of graphitic carbon(GC).While the cross-linked structure forms a compact interconnection network that allows electrons to rapid transfer between different GC frameworks.Electrochemical measurements demonstrated that the HGC anode exhibited low charge/discharge plateau(about 0.25 V and 0.1 V)and excellent specific capacity as high as 298 m A h g^(-1)at the current density of 50 m A g^(-1).And more important,after 200 cycles the capacity of HGC anode still shows 269 m A h g^(-1)(the decay rate of per cycle is only 0.048%).Meanwhile,the use of commercial traditional electrolyte(KPF_(6))and cheap raw materials that provide new hope for trying and realizing the large-scale production of PIBs based on carbon anode materials.展开更多
Chitosan (CS) microparticles with and without cross-linking were prepared by a water-in-oil emulsion solvent diffusion method without any surfactants. Aqueous CS solution and ethyl ace- tate were used as water and oil...Chitosan (CS) microparticles with and without cross-linking were prepared by a water-in-oil emulsion solvent diffusion method without any surfactants. Aqueous CS solution and ethyl ace- tate were used as water and oil phases, respectively. Genipin was used as a cross-linker. Influ- ences of genipin ratios and cross-linking times on CS microparticle characteristics were investigated. Non-cross-linked and cross-linked CS microparticles were spherical in shape and rough in surface. Microparticle matrices showed porous structures. Surface roughness, mean par- ticle sizes and bulk density of CS microparticles increased and their dissolutions in acetic acid solution decreased when genipin ratio and cross- linking time increased.展开更多
Microfluidic modulation spectroscopy(MMS)has been recognised as a novel technology for producing high quality and reproducible data at a wide concentration range to characterise protein structure.In this study,the use...Microfluidic modulation spectroscopy(MMS)has been recognised as a novel technology for producing high quality and reproducible data at a wide concentration range to characterise protein structure.In this study,the use of MMS for food applications was explored through the structural analysis of pea protein,whey protein,and pea/whey protein complexes prepared by transglutaminase cross-linking.MMS generated reproducible data with>99.5%repeatability in all protein samples.The cross-linking seemed to alter the structure of whey protein with isopeptide and hydrogen bond formation,more significantly than that of pea protein.The larger secondary and tertiary structural changes were observed with higher whey protein content in cross-linked pea/whey protein complex,which eventually increased the surface hydrophobicity.According to the second derivatives analysis by MMS,β-sheet and random coil increased andβ-turn decreased in the pea protein,whereasα-helix,β-sheet,andβ-turn decreased and random coil increased in the whey protein after cross-linking.In the pea/whey protein complex,β-turn shifted toβ-sheet due to cross-linking.There are some discrepancies between the relative secondary structure contents obtained from MMS data compared to the data acquired from circular dichroism.However,MMS has the considerable advantage of being able to directly measure original samples without significant dilution as required for circular dichroism measurements.This study provides evidence that MMS technology could be a robust technique to quantify the secondary structures of typical proteins in food with high reliability.展开更多
Cross-linkedβ-cyclodextrin polymer/Fe3O4 composite nanoparticles with core-shell structures were prepared via cross linking reaction on the surface of carboxymethylβ-cyclodextrin(CM-β-CD) modified Fe3O4 nanoparti...Cross-linkedβ-cyclodextrin polymer/Fe3O4 composite nanoparticles with core-shell structures were prepared via cross linking reaction on the surface of carboxymethylβ-cyclodextrin(CM-β-CD) modified Fe3O4 nanoparticles inβ-cyclodextrin alkaline solution by using epichlorohydrin as crosslinking agent.The morphology,structure and magnetic properties of the prepared composite nanoparticles were investigated by transmission electron microscopy(TEM),Fourier transform infrared(FTIR) spectrometry,X-ray diffraction(XRD) measurement,thermogravimetric analysis(TGA) and Vibrating sample magnetometry (VSM),respectively.展开更多
The macroporous anion exchangers with long-chained cross-linking agents were investigated for the tungsten recovery from salt solutions.The physical-chemical characteristics of these sorbents were studied by means of ...The macroporous anion exchangers with long-chained cross-linking agents were investigated for the tungsten recovery from salt solutions.The physical-chemical characteristics of these sorbents were studied by means of sorption-desorption experiment aswell as electron and IR-spectroscopy.The anion exchangers on the basis of macroporous copolymers of methylacrylate and divinyl-ester of diethyleneglycol or tetravinyl-ester of pentaerythritol possess the exchange capacity to tungsten 2--5 times greater than the porous anion exchangers on the basis of styrene and divinylbenzene,therefore they can be used for selective tungsten recovery from comulex salt solutions.展开更多
In order to prepare the polyethylene materials with controlling properties,we developed two kinds of controllable cross-linking polyethylene foaming system.2,5-dimethyl-2,5-bis (tert-butyl peroxy) hexane was used as c...In order to prepare the polyethylene materials with controlling properties,we developed two kinds of controllable cross-linking polyethylene foaming system.2,5-dimethyl-2,5-bis (tert-butyl peroxy) hexane was used as cross-linking agent and TEMPO as cross-linking inhibitor,azodicarbonamide (AC) was used as foaming agent and citric acid as foaming promoter.The density,expansion ratio,cellular structure and mechanical property of these two kinds of controllable materials were studied.Experimental results show that,properties of these two kinds of materials appear similar trend:cellular size and expansion ratio are enlarged with the amount of cross-linking inhibitor or foaming promoter increasing,while density and mechanical strength appear decreasing trend.Through comparing those two material systems’ properties,cross-linking polyethelene foaming system with citric acid as foaming promoter has better properties.展开更多
Protein structure and protein-protein interactions(PPIs)are crucial for regulating cellular activities required for cell viability and homeostasis.Chemical cross-linking coupled with mass spectrometry(CXMS)has become ...Protein structure and protein-protein interactions(PPIs)are crucial for regulating cellular activities required for cell viability and homeostasis.Chemical cross-linking coupled with mass spectrometry(CXMS)has become a versatile tool providing insights into both protein structure with distance restraints and protein-protein interactions with interface sites.Cross-links as the most information-rich data in a CXMS experiment are responsible for the structural model validation and integrative modeling with high throughput and sensitivity.In this work,ensemble refinement of the existing protein structure against the in-vivo cross-linking distance restraints was performed for dynamic protein structure modeling and protein interaction binding interface building in the intracellular environment.These results indicate great potential of in-vivo CXMS data for providing a molecular basis of protein structural dynamics exploration and function performance.展开更多
1 Introduction Immobilization of homogeneous catalysts onto polymer supports through covalent attachment has received wide attention because these materials offer advantage features of heterogeneous catalysis to homog...1 Introduction Immobilization of homogeneous catalysts onto polymer supports through covalent attachment has received wide attention because these materials offer advantage features of heterogeneous catalysis to homogeneous systems.The polymer-supported catalysts enhance their thermal stability,selectivity,recyclability and easy separation from reaction products leading to the operationally flexible[1-2].Such behaviour prompted us to know the effect of pore structures of polymer supporters on catalytic ...展开更多
The semi-interpenetrating network anion exchange membranes(AEMs)based on quaternized polyvinyl alcohol(QPVA)and poly(-diallyldimethylammonium chloride)(PDDA)are synthesized.The chemical cross-linking structure is form...The semi-interpenetrating network anion exchange membranes(AEMs)based on quaternized polyvinyl alcohol(QPVA)and poly(-diallyldimethylammonium chloride)(PDDA)are synthesized.The chemical cross-linking structure is formed between hydroxyl groups of QPVA and aldehyde groups of glutaraldehyde(GA),which makes PDDA more stable embed in the QPVA matrix and also improves the mechanical properties and dimensional stability of AEMs.Due to the phase separation phenomenon of AEMs swelling in water,a microporous structure may be formed in the membrane,which reduces the transmission resistance of hydroxide ions and provides a larger space for the transfer of hydroxide ions,thus improving the conductivity.The ring structure of PDDA is introduced as a cationic group to transfer hydroxide ions,and shields the nucleophilic attack of the hydroxide ions through the steric hindrance effect,which improves alkaline stability.The hydroxide conductivity of semi-interpenetrating network membrane(QPVA/PDDA0.5-GA)is 36.5 mS cm^(-1) at 60℃.And the membrane of QPVA/PDDA0.5-GA exhibits excellent mechanical property with maximum tensile strength of 19.6 MPa.After immersing into hot 3 mol L^(-1) NaOH solutions at 60℃ for 300 h,the OHconductivity remains 78%of its initial value.The semi-interpenetrating network AEMs with microporous structure exhibit good ionic conductivity,mechanical strength and alkaline durability.展开更多
The development of high-sulfur-loading Li-S batteries is a key prerequisite for their commercial applications.This requires to surmount the huge polarization,severe polysulfide shuttling and drastic volume change caus...The development of high-sulfur-loading Li-S batteries is a key prerequisite for their commercial applications.This requires to surmount the huge polarization,severe polysulfide shuttling and drastic volume change caused by electrode thickening.High-strength polar binders are ideal for constructing robust and long-life high-loading sulfur cathodes but show very weak interfacial interaction with non-polar sulfur materials.To address this issue,this work devises a highly integrated sulfur@polydopamine/highstrength binder composite cathodes,targeting long-lasting and high-sulfur-loading Li-S batteries.The super-adhesion polydopamine(PD)can form a uniform nano-coating over the graphene/sulfur(G-S)surface and provide strong affinity to the cross-linked polyacrylamide(c-PAM)binder,thus tightly integrating sulfur with the binder network and greatly boosting the overall mechanical strength/conductivity of the electrode.Moreover,the PD coating and c-PAM binder rich in polar groups can form two effective blockades against the effusion of soluble polysulfides.As such,the 4.5 mg cm−2 sulfur-loaded G-S@PD-c-PAM cathode achieves a capacity of 480 mAh g−1 after 300 cycles at 1 C,while maintaining a capacity of 396 mAh g−1 after 50 cycles at 0.2 C when the sulfur loading rises to 9.1 mg cm−2.This work provides a system-wide concept for constructing high-loading sulfur cathodes through integrated structural design.展开更多
文摘Cross-linked polyethylene (PEX) pipes used in hot water supply are required for high mechanical strength and high creep resistance at high temperature. Especially PEX-a pipes which are made by peroxide cross-linking have better performance, such as creep resistance and thermal shock resistance than the pipes made by the other cross-linking method. Because the PEX-a pipes indicate the higher cross-link degree as compared with the other PEX pipes. In this study, the PEX-a pipes which were mixed with several stabilizers were tested to evaluate the effects on cross-link degree and the oxygen induction time. And also they are evaluated with the chlorine aqueous solution by the performance of the long-term hydrostatic pressure test and the long-term hydro dynamic pressure test. As a result, it was found that the combination of antioxidants for PEX-a pipes plays an important role to prolong the oxygen induction time without inhibiting the cross-linking. From the results of the 1H pulsed NMR measurement over the melting point of polyethylene, it was found that each peroxide PEX pipe with different antioxidant combinations indicated the different proportion and crosslink density of cross-linked region, in addition, that these pipes had the effective structure of cross-linking for the hydrostatic and hydrodynamic pressure test with the chlorine aqueous solution. Therefore, it was considered to be useful results for studies of the stricture of cross-linking of polyethylene.
基金supported by National Natural Science Foundation of China(52103029 and 51903075).
文摘Polyimide(PI)is a promising electronic packaging material,but it remains challenging to obtain an all-organic PI hybrid film with decreased dielectric constant and loss without modifying the monomer.Herein,a series of allorganic PI hybrid films were successfully prepared by introducing the covalent organic framework(COF),which could induce the formation of the cross-linking structure in the PI matrix.Due to the synergistic effects of the COF fillers and the cross-linking structure,the PI/COF hybrid film containing 2 wt%COF exhibited the lowest dielectric constant of 2.72 and the lowest dielectric loss(tanδ)of 0.0077 at 1 MHz.It is attributed to the intrinsic low dielectric constant of COF and a large number of mesopores within the PI.Besides,the cross-linking network of PI prevents the molecular chains from stacking and improves the fraction of free volume(FFV).The molecular dynamics simulation results are well consistent with the dielectric properties data.Furthermore,the PI/COF hybrid film with 5 wt%COF showed a significant enhancement in breakdown strength,which increased to 412.8 kV/mm as compared with pure PI.In addition,the PI/COF hybrid film achieve to reduce the dielectric constant and thermal expansion coefficient(CTE).It also exhibited excellent thermal,hydrophobicity,and mechanical performance.The all-organic PI/COF hybrid films have great commercial potential as next-generation electronic packaging materials.
基金financially supported by National Natural Science Foundation of China(Nos.51922038 and 51672078)Hunan Outstanding Youth Talents(No.2019JJ20005)
文摘Large-scale and low-cost preparation of carbon-based potassium anode with long life and high capacity is one of the footstones for the development of potassium ion batteries(PIBs).Herein,a low-cost carbon-based material,cross-linked hollow graphitic carbon(HGC),is large scale synthesized to apply for PIBs anode.Its hollow structure can afford sufficient space to overcome the damage caused by the volume expansion of graphitic carbon(GC).While the cross-linked structure forms a compact interconnection network that allows electrons to rapid transfer between different GC frameworks.Electrochemical measurements demonstrated that the HGC anode exhibited low charge/discharge plateau(about 0.25 V and 0.1 V)and excellent specific capacity as high as 298 m A h g^(-1)at the current density of 50 m A g^(-1).And more important,after 200 cycles the capacity of HGC anode still shows 269 m A h g^(-1)(the decay rate of per cycle is only 0.048%).Meanwhile,the use of commercial traditional electrolyte(KPF_(6))and cheap raw materials that provide new hope for trying and realizing the large-scale production of PIBs based on carbon anode materials.
文摘Chitosan (CS) microparticles with and without cross-linking were prepared by a water-in-oil emulsion solvent diffusion method without any surfactants. Aqueous CS solution and ethyl ace- tate were used as water and oil phases, respectively. Genipin was used as a cross-linker. Influ- ences of genipin ratios and cross-linking times on CS microparticle characteristics were investigated. Non-cross-linked and cross-linked CS microparticles were spherical in shape and rough in surface. Microparticle matrices showed porous structures. Surface roughness, mean par- ticle sizes and bulk density of CS microparticles increased and their dissolutions in acetic acid solution decreased when genipin ratio and cross- linking time increased.
基金supported by ARC Discovery grant(DP200100642)supported by a PhD scholarship from the UNSW Sydney.
文摘Microfluidic modulation spectroscopy(MMS)has been recognised as a novel technology for producing high quality and reproducible data at a wide concentration range to characterise protein structure.In this study,the use of MMS for food applications was explored through the structural analysis of pea protein,whey protein,and pea/whey protein complexes prepared by transglutaminase cross-linking.MMS generated reproducible data with>99.5%repeatability in all protein samples.The cross-linking seemed to alter the structure of whey protein with isopeptide and hydrogen bond formation,more significantly than that of pea protein.The larger secondary and tertiary structural changes were observed with higher whey protein content in cross-linked pea/whey protein complex,which eventually increased the surface hydrophobicity.According to the second derivatives analysis by MMS,β-sheet and random coil increased andβ-turn decreased in the pea protein,whereasα-helix,β-sheet,andβ-turn decreased and random coil increased in the whey protein after cross-linking.In the pea/whey protein complex,β-turn shifted toβ-sheet due to cross-linking.There are some discrepancies between the relative secondary structure contents obtained from MMS data compared to the data acquired from circular dichroism.However,MMS has the considerable advantage of being able to directly measure original samples without significant dilution as required for circular dichroism measurements.This study provides evidence that MMS technology could be a robust technique to quantify the secondary structures of typical proteins in food with high reliability.
基金financially supported by the Guangdong Natural Science Foundation(No.020891)
文摘Cross-linkedβ-cyclodextrin polymer/Fe3O4 composite nanoparticles with core-shell structures were prepared via cross linking reaction on the surface of carboxymethylβ-cyclodextrin(CM-β-CD) modified Fe3O4 nanoparticles inβ-cyclodextrin alkaline solution by using epichlorohydrin as crosslinking agent.The morphology,structure and magnetic properties of the prepared composite nanoparticles were investigated by transmission electron microscopy(TEM),Fourier transform infrared(FTIR) spectrometry,X-ray diffraction(XRD) measurement,thermogravimetric analysis(TGA) and Vibrating sample magnetometry (VSM),respectively.
文摘The macroporous anion exchangers with long-chained cross-linking agents were investigated for the tungsten recovery from salt solutions.The physical-chemical characteristics of these sorbents were studied by means of sorption-desorption experiment aswell as electron and IR-spectroscopy.The anion exchangers on the basis of macroporous copolymers of methylacrylate and divinyl-ester of diethyleneglycol or tetravinyl-ester of pentaerythritol possess the exchange capacity to tungsten 2--5 times greater than the porous anion exchangers on the basis of styrene and divinylbenzene,therefore they can be used for selective tungsten recovery from comulex salt solutions.
基金Funded by National Natural Science Foundation of China (No.21975108)Fundamental Research Funds for the Central Universities of China (No.JUSRP121033)。
文摘In order to prepare the polyethylene materials with controlling properties,we developed two kinds of controllable cross-linking polyethylene foaming system.2,5-dimethyl-2,5-bis (tert-butyl peroxy) hexane was used as cross-linking agent and TEMPO as cross-linking inhibitor,azodicarbonamide (AC) was used as foaming agent and citric acid as foaming promoter.The density,expansion ratio,cellular structure and mechanical property of these two kinds of controllable materials were studied.Experimental results show that,properties of these two kinds of materials appear similar trend:cellular size and expansion ratio are enlarged with the amount of cross-linking inhibitor or foaming promoter increasing,while density and mechanical strength appear decreasing trend.Through comparing those two material systems’ properties,cross-linking polyethelene foaming system with citric acid as foaming promoter has better properties.
基金This work was supported by the R&D Program of China(No.2018YFA0507703)the National Natural Science Foundation of China(Nos.22074139,21991083,32088101,21775150)+1 种基金the CAS Key Project in Frontier Science(No.QYZDY-SSW-SLH017)the Youth Innovation Promotion Association,CAS(No.2020184).
文摘Protein structure and protein-protein interactions(PPIs)are crucial for regulating cellular activities required for cell viability and homeostasis.Chemical cross-linking coupled with mass spectrometry(CXMS)has become a versatile tool providing insights into both protein structure with distance restraints and protein-protein interactions with interface sites.Cross-links as the most information-rich data in a CXMS experiment are responsible for the structural model validation and integrative modeling with high throughput and sensitivity.In this work,ensemble refinement of the existing protein structure against the in-vivo cross-linking distance restraints was performed for dynamic protein structure modeling and protein interaction binding interface building in the intracellular environment.These results indicate great potential of in-vivo CXMS data for providing a molecular basis of protein structural dynamics exploration and function performance.
文摘1 Introduction Immobilization of homogeneous catalysts onto polymer supports through covalent attachment has received wide attention because these materials offer advantage features of heterogeneous catalysis to homogeneous systems.The polymer-supported catalysts enhance their thermal stability,selectivity,recyclability and easy separation from reaction products leading to the operationally flexible[1-2].Such behaviour prompted us to know the effect of pore structures of polymer supporters on catalytic ...
基金The authors gratefully acknowledge the financial support of this work by Natural Science Foundation of China(grant no.s 51673030,51603017 and 51803011)Jilin Provincial Science&Technology Department(grant no.s 20200801011GH,20180101209JC,20160520138JH,20160519020JH)+1 种基金Jilin Province Development and Reform Commission(Grant nos:2019C042-5)ChangBai Mountain Scholars Program of Jilin Province.
文摘The semi-interpenetrating network anion exchange membranes(AEMs)based on quaternized polyvinyl alcohol(QPVA)and poly(-diallyldimethylammonium chloride)(PDDA)are synthesized.The chemical cross-linking structure is formed between hydroxyl groups of QPVA and aldehyde groups of glutaraldehyde(GA),which makes PDDA more stable embed in the QPVA matrix and also improves the mechanical properties and dimensional stability of AEMs.Due to the phase separation phenomenon of AEMs swelling in water,a microporous structure may be formed in the membrane,which reduces the transmission resistance of hydroxide ions and provides a larger space for the transfer of hydroxide ions,thus improving the conductivity.The ring structure of PDDA is introduced as a cationic group to transfer hydroxide ions,and shields the nucleophilic attack of the hydroxide ions through the steric hindrance effect,which improves alkaline stability.The hydroxide conductivity of semi-interpenetrating network membrane(QPVA/PDDA0.5-GA)is 36.5 mS cm^(-1) at 60℃.And the membrane of QPVA/PDDA0.5-GA exhibits excellent mechanical property with maximum tensile strength of 19.6 MPa.After immersing into hot 3 mol L^(-1) NaOH solutions at 60℃ for 300 h,the OHconductivity remains 78%of its initial value.The semi-interpenetrating network AEMs with microporous structure exhibit good ionic conductivity,mechanical strength and alkaline durability.
基金supported by the National Natural Science Foundation of China(21875155,51675275,21703185 and 21473119)Q.B.Z.acknowledges the Leading Project Foundation of Science Department of Fujian Province(2018H0034)Shenzhen Science and Technology Planning Project(JCYJ20170818153427106).
文摘The development of high-sulfur-loading Li-S batteries is a key prerequisite for their commercial applications.This requires to surmount the huge polarization,severe polysulfide shuttling and drastic volume change caused by electrode thickening.High-strength polar binders are ideal for constructing robust and long-life high-loading sulfur cathodes but show very weak interfacial interaction with non-polar sulfur materials.To address this issue,this work devises a highly integrated sulfur@polydopamine/highstrength binder composite cathodes,targeting long-lasting and high-sulfur-loading Li-S batteries.The super-adhesion polydopamine(PD)can form a uniform nano-coating over the graphene/sulfur(G-S)surface and provide strong affinity to the cross-linked polyacrylamide(c-PAM)binder,thus tightly integrating sulfur with the binder network and greatly boosting the overall mechanical strength/conductivity of the electrode.Moreover,the PD coating and c-PAM binder rich in polar groups can form two effective blockades against the effusion of soluble polysulfides.As such,the 4.5 mg cm−2 sulfur-loaded G-S@PD-c-PAM cathode achieves a capacity of 480 mAh g−1 after 300 cycles at 1 C,while maintaining a capacity of 396 mAh g−1 after 50 cycles at 0.2 C when the sulfur loading rises to 9.1 mg cm−2.This work provides a system-wide concept for constructing high-loading sulfur cathodes through integrated structural design.