Self-healing superhydrophobic polyvinylidene fluoride/Fe3O4@polypyrrole （F- PVDF/FeBO4@PPyx） fibers with core-sheath structure were successfully fabricated by electrospinning of a PVDF/Fe3O4 mixture and in situ chem...Self-healing superhydrophobic polyvinylidene fluoride/Fe3O4@polypyrrole （F- PVDF/FeBO4@PPyx） fibers with core-sheath structure were successfully fabricated by electrospinning of a PVDF/Fe3O4 mixture and in situ chemical oxidative polymerization of pyrrole, followed by chemical vapor deposition with fluoroalkyl silane. The F-PVDF/Fe3O4@PPy0.075 fiber film produces a superhydrophobic surface with self-healing behavior, which can repetitively and automatically restore superhydrophobicity when the surface is chemically damaged. Moreover, the maximum refection loss （Ru） of the F-PVDF/Fe304@PPy0.075 fiber film reaches -21.5 dB at 16.8 GHz and the RL below -10 dB is in the frequency range of 10.6-16.5 GHz with a thickness of 2.5 mm. The microwave absorption performance is attributed to the synergetic effect between dielectric loss and magnetic loss originating from PPy, PVDF and Fe3O4. As a consequence, preparing such F-PVDF/Fe3O4@PPyx fibers in this manner provides a simple and effective route to develop multi-functional microwave absorbing materials for practical applications.展开更多
Ultrafine polycaprolactone(PCL)fibers containing watersoluble drug tetracycline hydrochloride(Tet)were prepared by emulsion electrospinning.Sorbitan monooleate(Span80)was added as an essential additive to form stable ...Ultrafine polycaprolactone(PCL)fibers containing watersoluble drug tetracycline hydrochloride(Tet)were prepared by emulsion electrospinning.Sorbitan monooleate(Span80)was added as an essential additive to form stable water/oil emulsions and fabricate fibers with core-sheath structure.Different concentrations of Span80(0-40 g/L)were used to investigate the stability of emulsion and size of dispersed droplets.The scanning electron microscope(SEM)images indicated that the morphology of the fibers with Span80 were beaded-free with diameters of 200-400 nm,and Span80 enhanced the spinnability of electrospinning solution.The laser scanning confocal microscope(LSCM)images indicated that Tet was well encapsulated into the core region of the PCL fibers.The transmission electron microscope(TEM)image showed the formation of core-sheath structure.The loading efficiency(LE)and entrapment efficiency(EE)of Tet were calculated and release profiles in artificial saliva buffer solution(pH=6.8)were also analyzed.The results revealed that LE and EE of fibers with Span80decreased with the increase of its concentration.Fibers with coresheath structure had a longer effective release lifetime than without Span80.The increase of Span80 resulted in higher hydrophilicity of fibers and faster release rate of Tet.展开更多
One-dimensional(1D)oxide nanofibers have attracted much attention in recent years but are still hampered by the difficulty in the expansion to 2D or 3D dimensions.Herein,ultrathin CeO_(2)/SiO_(2)nanofibers with intrig...One-dimensional(1D)oxide nanofibers have attracted much attention in recent years but are still hampered by the difficulty in the expansion to 2D or 3D dimensions.Herein,ultrathin CeO_(2)/SiO_(2)nanofibers with intriguing core-sheath structures were simply fabricated by a facile single-spinneret electrospinning method and were subsequently integrated as 2D nanofi-brous mats and 3D sponges.Introducing secondary oxide(i.e.,SiO_(2))could induce a unique fine structure and further inhibit the sintering of CeO_(2)nanocrystals,endowing the resultant dual-oxide nanofibers with high porosity,good flexibility,and enriched oxygen defects.Benefiting from the core-sheath structure and dual-oxide component,the CeO_(2)/SiO_(2)nanofibers could stabilize 2.59 nm-Pt clusters against sintering at 600℃.Once assembled into a 2D mat,the nanofibers could efficiently decrease the soot oxidation temperature by 63℃.Moreover,the core-sheath CeO_(2)/SiO_(2)nanofibers can be readily integrated with graphene nanosheets into a 3D sponge via a gas foaming protocol,showing 218.5 mg/g of adsorption capacity toward Rhodamine B molecules.This work shed lights on the versatile applications of oxide nanofibers toward clean energy ultili-zation and low-carbon development.展开更多
以再生丝素蛋白水溶液为皮层纺丝液,去离子水为芯层纺丝液,探讨了同轴静电纺制备丝素蛋白组织工程支架材料的最佳工艺参数。结果表明,随着皮层纺丝液质量分数的提高,支架材料的表观形貌逐渐变好;当皮层纺丝液的质量分数为39%(w)、流速为...以再生丝素蛋白水溶液为皮层纺丝液,去离子水为芯层纺丝液,探讨了同轴静电纺制备丝素蛋白组织工程支架材料的最佳工艺参数。结果表明,随着皮层纺丝液质量分数的提高,支架材料的表观形貌逐渐变好;当皮层纺丝液的质量分数为39%(w)、流速为1.2 m L/h,芯层纺丝液流速为0.3 m L/h时,可制备出表观形貌好、纤维粗细均匀且具有稳定皮芯结构的支架材料。文章探索得到的同轴静电纺丝工艺可用于载药组织工程支架材料的制备,并在组织工程修复领域具有良好的应用前景。展开更多
基金The work is supported by the National Natural Sdence Foundation of China （Nos. 51273008, 51473008, and 21103006）, Beijing Natural Science Foundation （No. 2132030） and the National Basic Research Program of China （No. 2012CB933200）.
文摘Self-healing superhydrophobic polyvinylidene fluoride/Fe3O4@polypyrrole （F- PVDF/FeBO4@PPyx） fibers with core-sheath structure were successfully fabricated by electrospinning of a PVDF/Fe3O4 mixture and in situ chemical oxidative polymerization of pyrrole, followed by chemical vapor deposition with fluoroalkyl silane. The F-PVDF/Fe3O4@PPy0.075 fiber film produces a superhydrophobic surface with self-healing behavior, which can repetitively and automatically restore superhydrophobicity when the surface is chemically damaged. Moreover, the maximum refection loss （Ru） of the F-PVDF/Fe304@PPy0.075 fiber film reaches -21.5 dB at 16.8 GHz and the RL below -10 dB is in the frequency range of 10.6-16.5 GHz with a thickness of 2.5 mm. The microwave absorption performance is attributed to the synergetic effect between dielectric loss and magnetic loss originating from PPy, PVDF and Fe3O4. As a consequence, preparing such F-PVDF/Fe3O4@PPyx fibers in this manner provides a simple and effective route to develop multi-functional microwave absorbing materials for practical applications.
基金“111 Project” Biomedical Textile Materials Science and Technology,China(No.B07024)
文摘Ultrafine polycaprolactone(PCL)fibers containing watersoluble drug tetracycline hydrochloride(Tet)were prepared by emulsion electrospinning.Sorbitan monooleate(Span80)was added as an essential additive to form stable water/oil emulsions and fabricate fibers with core-sheath structure.Different concentrations of Span80(0-40 g/L)were used to investigate the stability of emulsion and size of dispersed droplets.The scanning electron microscope(SEM)images indicated that the morphology of the fibers with Span80 were beaded-free with diameters of 200-400 nm,and Span80 enhanced the spinnability of electrospinning solution.The laser scanning confocal microscope(LSCM)images indicated that Tet was well encapsulated into the core region of the PCL fibers.The transmission electron microscope(TEM)image showed the formation of core-sheath structure.The loading efficiency(LE)and entrapment efficiency(EE)of Tet were calculated and release profiles in artificial saliva buffer solution(pH=6.8)were also analyzed.The results revealed that LE and EE of fibers with Span80decreased with the increase of its concentration.Fibers with coresheath structure had a longer effective release lifetime than without Span80.The increase of Span80 resulted in higher hydrophilicity of fibers and faster release rate of Tet.
基金This work was financially supported by the Natural Science Foundation of China(21975042)the Project of Six Talents Climax Foundation of Jiangsu(XCL-082)+3 种基金Innovation Platform Project Supported by Jiangsu Province(6907041203)the Young Talent Lifting Project of Jiangsu Science and Technology Associate,the Fundamental Research Funds for the Central Universities,the Postgraduate Research&Practice Innovation Program of Jiangsu Province(KYCX22_0261)the Priority Academic Program Development of Jiangsu Higher Education Institutionsthe open project of State Key Laboratory of Physical Chemistry of Solid Surfaces in Xiamen University.
文摘One-dimensional(1D)oxide nanofibers have attracted much attention in recent years but are still hampered by the difficulty in the expansion to 2D or 3D dimensions.Herein,ultrathin CeO_(2)/SiO_(2)nanofibers with intriguing core-sheath structures were simply fabricated by a facile single-spinneret electrospinning method and were subsequently integrated as 2D nanofi-brous mats and 3D sponges.Introducing secondary oxide(i.e.,SiO_(2))could induce a unique fine structure and further inhibit the sintering of CeO_(2)nanocrystals,endowing the resultant dual-oxide nanofibers with high porosity,good flexibility,and enriched oxygen defects.Benefiting from the core-sheath structure and dual-oxide component,the CeO_(2)/SiO_(2)nanofibers could stabilize 2.59 nm-Pt clusters against sintering at 600℃.Once assembled into a 2D mat,the nanofibers could efficiently decrease the soot oxidation temperature by 63℃.Moreover,the core-sheath CeO_(2)/SiO_(2)nanofibers can be readily integrated with graphene nanosheets into a 3D sponge via a gas foaming protocol,showing 218.5 mg/g of adsorption capacity toward Rhodamine B molecules.This work shed lights on the versatile applications of oxide nanofibers toward clean energy ultili-zation and low-carbon development.
文摘以再生丝素蛋白水溶液为皮层纺丝液,去离子水为芯层纺丝液,探讨了同轴静电纺制备丝素蛋白组织工程支架材料的最佳工艺参数。结果表明,随着皮层纺丝液质量分数的提高,支架材料的表观形貌逐渐变好;当皮层纺丝液的质量分数为39%(w)、流速为1.2 m L/h,芯层纺丝液流速为0.3 m L/h时,可制备出表观形貌好、纤维粗细均匀且具有稳定皮芯结构的支架材料。文章探索得到的同轴静电纺丝工艺可用于载药组织工程支架材料的制备,并在组织工程修复领域具有良好的应用前景。
基金financially supported by the National Natural Science Foundation of China(51973079)the Science and Technology Development Plan of Jilin Province,China(20220402008GH)。
文摘设计分层异质结构作为一种经济且高效的催化剂,以实现水分解的电子和界面工程,是能源存储与转化中的一个有意义的决策.在这项工作中,通过静电纺丝-碳化-电沉积的策略,制备了负载在嵌入Co纳米颗粒的碳纤维上的非晶态NiFeS纳米片(Co-C/NiFeS纳米纤维)催化剂.该催化剂具有优异的析氧反应(OER)活性,在1 mol L^(-1)KOH溶液中,在10 mA cm^(-2)下的过电位为233 mV,Tafel斜率为53.1 mV dec^(-1),同时还具有良好的析氢反应活性.此外,由Co-C/NiFeS纳米纤维作为阳极,商用Pt/C作为阴极构建的碱性Pt/C‖Co-C/NiFeS电解槽在10 mA cm^(-2)下实现1.48 V的低电池电压,优于基准Pt/C‖RuO_(2)电解槽和许多其他报道的电解槽.作为双功能电催化剂,Co-C/NiFeS‖Co-C/NiFeS自身组装的电解槽表现出70小时的长期稳定性,显著优于Pt/C‖RuO_(2)电解槽.该催化剂显著的OER性能得益于Co-C纳米纤维核与非晶NiFeS纳米片鞘组成的明显分层异质结构以及生成的高导电碳纤维基底,这些结构特征赋予该材料丰富的暴露活性位点、良好的导电性和坚固的结构稳定性.因此,这项工作提出了一种简单且有效的方法来制备具有优异电催化性能的非贵金属基催化剂,以用于实际的能量转换和存储.
