Developing high-performance non-precious metal electrocatalysts for oxygen reduction reaction(ORR)is crucial for the commercialization of fuel cells and metal-air batteries.However,doped carbon-based materials only sh...Developing high-performance non-precious metal electrocatalysts for oxygen reduction reaction(ORR)is crucial for the commercialization of fuel cells and metal-air batteries.However,doped carbon-based materials only show good ORR activity in alkaline medium,and become less effective in acidic environment.We believe that an appropriate combination of both ionic and electronic transport path,and well dopant distribution of doped carbon-based materials would help to realize high ORR performance un-der both acidic and alkaline cond让ions.Accordingly,a nitrogen and sulfur co-doped carbon framework with hierarchical through-hole structure is fabricated by morphology-controlled solid-state pyrolysis of poly(aniline-co-2-ami no thiophenol)foam.The uniform high concentrations of nitrogen and sulfur,high intrinsic conductivity,and integrated three dimensional ionic and electronic transfer passageways of the 3D porous structure lead to synergistic effects in catalyzing ORR.As a result,the limiting current density of the carbonized poly(aniline-co-2-aminothiophenol)foam is equivalent to commercial Pt/C in acidic environment,and twice the latter in alkaline medium.展开更多
To tackle the challenge of producing highly filled polymer composites using the traditional injection molding technique,which is characterized by the fairly high melt viscosity that makes mold filling difficult,the au...To tackle the challenge of producing highly filled polymer composites using the traditional injection molding technique,which is characterized by the fairly high melt viscosity that makes mold filling difficult,the authors propose a solution based on dynamic covalent chemistry.As demonstrated by the proof-of-concept experiments,the 4-arm starshaped polycaprolactone(PCL)oligomers and microcrystalline cel-lulose(MCC)are crosslinked by the reversible Diels-Alder(DA)bonds.The flowability of the compounds greatly decreases due to the dissociation of the intercomponent DA bonds at the retro-reaction tempera-ture,and the networked architecture is reconstructed during cooling as a result of the forward DA reaction.Consequently,the high-loading MCC fillers are well distributed in the matrix and covalently bonded to the nearby PCL,forming a striking contrast to the control in which linear PCL acts as the matrix.The DA bonds crosslinked biodegradable PCL composites exhibit decent mechanical strength(20.7 MPa)even at the MCC fraction of 65 wt%,which is superior to those(5-12.2 MPa)of the highly filled PCL composites(with filler contents of 50-63.8 wt%)reported so far.The proposed approach has sufficient expansibility for the fabrication of the highly filled polymer composites constructed by other types of matrix and fillers.展开更多
To change the situation of shape memory polymers(SMPs)that can only remember very few shapes and enable discretional morphing for practical application,the authors report a reversible stepless multiple SMP derived fro...To change the situation of shape memory polymers(SMPs)that can only remember very few shapes and enable discretional morphing for practical application,the authors report a reversible stepless multiple SMP derived from ultrahigh molecular weight polyethylene(UHMWPE).As the crystals of semicrystalline polymers are assembled by those with slightly different melting temperatures,and each type of crystal can remember a single shape,the crystalline region of UHMWPE is allowed to remember plenty of temporary shapes after programming.Changing the temperature of the programmed polymer within the melting/crystallization temperature ranges would lead to releasing/recovery of the memorized temporary shapes.Accordingly,multiple shape memory effects can be easily realized without an elaborate design of material structure and training process in advance as before.The temperaturedependent adjustability of the analog capacitor and soft lens with embedded programmed UHMWPE as actuators,characterized by the continuous/random/proportional responsivity,further reveals the utilization prospects of the controllable reversible stepless discretionary morphing effect.Moreover,the maximum work density of the programmed UHMWPE is found to be 210 kJ/m_(3),which is more than 10 times of piezoelectric ceramics,so that it can serve as a proof-of-concept mechanical driver for reversibly pumping of ethanediol-droplet upon heating/cooling.展开更多
基金financial support by the National Natural Science Foundation of China (Grant: 51333008)Young Teacher Training Program of Sun Yat-sen University (Grant: 17lgpy86)
文摘Developing high-performance non-precious metal electrocatalysts for oxygen reduction reaction(ORR)is crucial for the commercialization of fuel cells and metal-air batteries.However,doped carbon-based materials only show good ORR activity in alkaline medium,and become less effective in acidic environment.We believe that an appropriate combination of both ionic and electronic transport path,and well dopant distribution of doped carbon-based materials would help to realize high ORR performance un-der both acidic and alkaline cond让ions.Accordingly,a nitrogen and sulfur co-doped carbon framework with hierarchical through-hole structure is fabricated by morphology-controlled solid-state pyrolysis of poly(aniline-co-2-ami no thiophenol)foam.The uniform high concentrations of nitrogen and sulfur,high intrinsic conductivity,and integrated three dimensional ionic and electronic transfer passageways of the 3D porous structure lead to synergistic effects in catalyzing ORR.As a result,the limiting current density of the carbonized poly(aniline-co-2-aminothiophenol)foam is equivalent to commercial Pt/C in acidic environment,and twice the latter in alkaline medium.
基金the support of the National Natural Science Foundation of China(Grants:52033011,51973237,and 52173092)Natural Science Foundation of Guangdong Province(Grants:2019B1515120038,2020A1515011276,2021A1515010417)+1 种基金Science and Technology Planning Project of Guangzhou City(Grant:202201011568)Fundamental Research Funds for the Central Universities,Sun Yatsen University(Grant:23yxqntd002).
文摘To tackle the challenge of producing highly filled polymer composites using the traditional injection molding technique,which is characterized by the fairly high melt viscosity that makes mold filling difficult,the authors propose a solution based on dynamic covalent chemistry.As demonstrated by the proof-of-concept experiments,the 4-arm starshaped polycaprolactone(PCL)oligomers and microcrystalline cel-lulose(MCC)are crosslinked by the reversible Diels-Alder(DA)bonds.The flowability of the compounds greatly decreases due to the dissociation of the intercomponent DA bonds at the retro-reaction tempera-ture,and the networked architecture is reconstructed during cooling as a result of the forward DA reaction.Consequently,the high-loading MCC fillers are well distributed in the matrix and covalently bonded to the nearby PCL,forming a striking contrast to the control in which linear PCL acts as the matrix.The DA bonds crosslinked biodegradable PCL composites exhibit decent mechanical strength(20.7 MPa)even at the MCC fraction of 65 wt%,which is superior to those(5-12.2 MPa)of the highly filled PCL composites(with filler contents of 50-63.8 wt%)reported so far.The proposed approach has sufficient expansibility for the fabrication of the highly filled polymer composites constructed by other types of matrix and fillers.
基金Guangdong Basic and Applied Basic Research Foundation,Grant/Award Number:2019A1515110327Science Foundation for Young Teachers of Wuyi University,Grant/Award Number:2018AL017+4 种基金Innovation and Entrepreneurship Foundation of Students of Wuyi University,Grant/Award Number:2020CX16National Natural Science Foundation of China,Grant/Award Numbers:52003201,52033011Guangdong Science and Technology Major Special Fund,Grant/Award Number:2019-252Science Foundation for Young Research Group of Wuyi University,Grant/Award Number:2019td08Joint Research Fund for Wuyi University,Hong Kong and Macao Young Scholars,Grant/Award Number:2019WGALH05。
文摘To change the situation of shape memory polymers(SMPs)that can only remember very few shapes and enable discretional morphing for practical application,the authors report a reversible stepless multiple SMP derived from ultrahigh molecular weight polyethylene(UHMWPE).As the crystals of semicrystalline polymers are assembled by those with slightly different melting temperatures,and each type of crystal can remember a single shape,the crystalline region of UHMWPE is allowed to remember plenty of temporary shapes after programming.Changing the temperature of the programmed polymer within the melting/crystallization temperature ranges would lead to releasing/recovery of the memorized temporary shapes.Accordingly,multiple shape memory effects can be easily realized without an elaborate design of material structure and training process in advance as before.The temperaturedependent adjustability of the analog capacitor and soft lens with embedded programmed UHMWPE as actuators,characterized by the continuous/random/proportional responsivity,further reveals the utilization prospects of the controllable reversible stepless discretionary morphing effect.Moreover,the maximum work density of the programmed UHMWPE is found to be 210 kJ/m_(3),which is more than 10 times of piezoelectric ceramics,so that it can serve as a proof-of-concept mechanical driver for reversibly pumping of ethanediol-droplet upon heating/cooling.
