基于铅笔芯和多巴胺电聚合膜固定葡萄糖氧化酶的高灵敏酶电极

市售8B铅笔芯经镀铂处理后,将葡萄糖氧化酶共沉积到新型多巴胺电氧化聚合膜中,最外层再修饰聚邻氨基酚薄膜,研制出新型葡萄糖氧化酶修饰电极用于葡萄糖检测.

3,4-乙烯二氧噻吩单体用作锂离子电池安全性改善添加剂的研究

安全性是制约锂离子电池向电动汽车领域应用拓展的主要障碍之一.本工作提出了一种能够有效改善锂离子电池安全性的电解液添加剂3,4-乙烯二氧噻吩单体(EDOT),研究了EDOT在有机电解液中的电氧化聚合行为及其对Li Co O2电极高温热行为和电池安全性、电化学性能的影响.循环伏安(CV)和透射电镜(TEM)表征结果表明,单体添加剂能够在电池充电过程发生电氧化聚合,在正极表面形成一层聚(3,4-乙烯二氧噻吩)(PEDOT)导电聚合物膜.差示扫描量热(DSC)分析结果显示,PEDOT隔离了电解液与正极表面的直接接触,减少了过热条件下电解液在正极表面的分解放热.安全性测试结果表明,在电解液中仅添加0.1%的EDOT单体,即可将电池在150oC高温热冲击下发生热失控的时间推迟13.8 min.电化学性能测试结果表明,聚合产物良好的电子导电性能有效改善正极的电子传导能力,在一定程度上提高电池的倍率性能和循环稳定性,而容量、低温性能等基本不受影响,展示出良好的应用前景.

Electro‑copolymerized film of ruthenium catalyst and redox mediator for electrocatalytic water oxidation

Electro-copolymerized film containing ruthenium complexes as electron-transfer(or redox)mediators and water-oxidation catalysts by an oxidative copolymerization method is presented.The addition of the redox mediator significantly improved the electrocatalytic water-oxidation activity and reduced the overpotential to 220 mV.The prepared electrode showed a water-oxidation catalytic rate constant kobs of 31.7 s^(-1)and an initial turnover frequency of 1.01 s^(-1)in 1000 s by potential electrolysis at 1.7 V applied bias vs NHE(normal hydrogen electrode).The kinetic isotope effect study suggests that the catalytic water oxidation reaction on the electrode surface occurs via a bimolecular coupling mechanism.

Identification of origin of insulating polymer maneuvered photoredox catalysis

Solid non-conjugated polymers have long been regarded as insulators due to deficiency of delocalizedπelectrons along the molecular chain framework.Up to date,origin of insulating polymer regulated charge transfer has not yet been uncovered.In this work,we unleash the root origin of charge transport capability of insulating polymer in photocatalysis.We ascertain that insulating polymer plays crucial roles in fine tuning of electronic structure of transition metal chalcogenides(TMCs),which mainly include altering surface electron density of TMCs for accelerating charge transport kinetics,triggering the generation of defect over TMCs for prolonging carrier lifetime,and acting as hole-trapping mediator for retarding charge recombination.These synergistic roles contribute to the charge transfer of insulating polymer.Our work opens a new vista of utilizing solid insulating polymers for maneuvering charge transfer toward solar energy conversion.

Electro-polymerization fabrication of PANI@GF electrode and its energy-effective electrocatalytic performance in electro-Fenton process

An energy-effective polyaniline coated graphite felt （PANI@GF） composite cathode for the elec- tro-Fenton （E-Fenton） process was synthesized through an electro-polymerization method. The electrocatalytic activity of the cathode for the 2e- ORR process was investigated and dimethyl phthalate （DMP） was used as a model substrate to evaluate its performance in the E-Fenton process. The as-prepared PANI@GF composite possessed a three-dimensional porous structure, which is favorable for 02 diffusion, while the large amount of N atoms in the conductive polyaniline （PANI） enhanced 2e- ORR reactivity. The DMP degradation of the E-Fenton system using PANI@GF was significantly enhanced owing to the improvement in ORR performance. The apparent kinetic con- stant for DMP degradation was 0.0753 min-1, five times larger than that of GF. The optimal carboni- zation temperature and polymerization time for the preparation of the PANI@GF composite cath- ode was found to be 900 ℃ and 1 h, respectively. Measurement conditions are a crucial factor for proper evaluation of cathode electrocatalytic performance. Accordingly, the 02 flow rate, Fe^2＋ con- centration, and pH for DMP degradation were optimized at 0.4 L/min, 1.0 mmol/L, and 3.0, respec- tively. These results indicate that the present PANI@GF composite cathode is energy-effective and promising for potential use as an E-Fenton system cathode for the removal of organic pollutants in wastewater.

Enhanced dielectric permittivity of graphite oxide/polyimide composite films

Graphite oxide(GO) was prepared by the pressurized oxidation method and incorporated into polyimide(PI) matrix to fabricate high-k composite films by in-situ polymerization and subsequent thermal treatment. The results show that the as-prepared GO had good dispersion and compatibility in PI matrix due to the introduction of abundant oxygen-containing functional groups during the oxidation. The residual graphitic domains and the thermal treatment induced reduction of GO further enhanced the dielectric permittivity of the resulting GO–PI composites. The dielectric permittivity of the GO–PI composites exhibited a typical percolation behavior with a percolation threshold of 0.0347 of volume ratio and a critical exponent of 0.837. Near the percolation threshold, the dielectric permittivity of the GO–PI composite increased to 108 at 10~2 Hz and was 26 times that of the pure PI.

Effect of current density on corrosion resistance of micro-arc oxide coatings on magnesium alloy

Oxide coatings were prepared on magnesium alloys in electrolyte solution of Na2SiO3 at different current densities(3,4 and 5 A/cm 2 )with micro-arc oxidation process.X-ray diffractometry(XRD)results show that the oxide coatings formed on magnesium alloys are mainly composed of MgO and MgAl2O4 phases;in addition,the content of MgO increases with increasing the current density.The morphology and surface roughness of the coatings were characterized by confocal laser scanning microscopy (CLSM).The results show that the surface roughness(Ra)decreases with increasing the current density.Moreover,the electrochemical corrosion results prove that the MgO coating produced in the electrolyte Na2SiO3 at current density of 5 A/cm 2 shows the best corrosion resistance.

Preparation and properties of composite polymer electrolyte modified with nano-size rare earth oxide

Poly（vinylidene fluoride-co-hexafluoropropylene） （PVDF-HFP） based composite polymer electrolyte （CPE） modified with CeO2, La2O3 and Y2O3 nano-rare earth oxides was prepared by phase inversion technique. Physical and chemical properties of the modified CPEs were studied by SEM, TG-DSC and electrochemical methods. The results show that the CPE modified with 10% La2O3 （mass fraction） has the best practical applicability, which indicates that the thermal and electrochemical stability can reach over 400 ℃ and 4.5 V, respectively, and temperature dependence of ionic conductivity follows Vogel-Tamman-Fulcher （VTF） relationship and ionic conductivity at room temperature is up to 3.3 mS/cm. The interfacial resistance Ri reaches a stable value about 557 Ω after 6 d storage.

Electrochemical performance of interfacially polymerized polyaniline nanofibres as electrode materials for non-aqueous redox supercapacitors

H+ doped polyaniline nanofibre(PH) was synthesized by interfacial polymerization and polyanilines doped with Li salt(PLI and PHLI) were prepared by immersing emeraldine base(EB) and H+ doped polyaniline in 1 mol/L LiPF6/(EC-EMC-DMC),respectively.PH,PLI and PHLI were all characterized by scanning electron microscopy(SEM) and Fourier transform infrared(FT-IR) spectrometry.With 1 mol/L LiPF6/(EC-EMC-DMC) as electrolyte,PH,PHLI and PLI were used as the active materials of symmetric non-aqueous redox supercapacitors.PLI shows the highest initial specific capacitance of 120 F/g(47 F/g for PH and 66 F/g for PHLI) among three samples.After 500 cycles,the specific capacitance of PLI remains 75 F/g,indicating the good cycleability.

Solution-processed copper nanowire flexible transparent electrodes with PEDOT：PSS as binder, protector and oxide-layer scavenger for polymer solar cells

The easy oxidation and surface roughness of Cu nanowire （NW） films are the main bottlenecks for their usage in transparent conductive electrodes （TCEs）. Herein, we have developed a facile and scaled-up solution route to prepare Cu NW-based TCEs by embedding Cu NWs into pre-coated smooth poly（3,4-ethylenedioxythiophene）：poly（styrenesulfonate） （PEDOT：PSS） films on poly（ethylene terephthalate） （PET） substrates. The so obtained Cu NW- PEDOT：PSS/PET films have low surface roughness （-70 nm in height）, high stability toward oxidation and good flexibility. The optimal TCEs show a typical sheet resistance of 15Ω·sq-1 at high transparency （76% at A = 550 nm） and have been used successfully to make polymer （poly（3-hexylthiophene）：phenyl-C61- butyric acid methyl ester） solar cells, giving an efficiency of 1.4%. The overall properties of Cu NW-PEDOT：PSS/PET films demonstrate their potential application as a replacement for indium tin oxide in flexible solar cells.

In-situ electropolymerized bipolar organic cathode for stable and high-rate lithium-ion batteries

To address the dissolution issue and enhance the electrochemical performance of organic electrode materials,herein, a bipolar organic cathode was prepared by in-situ electropolymerization of amino-phenyl carbazole naphthalene diimide(APCNDI). APCNDI is composed of n-type 1,4,5,8-naphthalene tetracarboxylic diimide that stores Li cations and p-type carbazole groups which react with anions and serve as polymerization sites. Electropolymerization completely eliminated the dissolution problem of APCNDI, and the electropolymerized cathode demonstrated a bipolar reaction with excellent electrochemical performance, stable cycling performance with a capacity retention of 92 mA h g;after1000 cycles, and a superior rate performance of 72 mA h g;at 10 A g;. The bipolar feature and reactions of APCNDI were systematically investigated and verified by multiple characterization techniques. Our findings provide a novel strategy for the design and fabrication of electrodes for high-performance organic batteries.

Three-dimensional nitrogen and phosphorous Co-doped graphene aerogel electrocatalysts for efficient oxygen reduction reaction

The development of efficient electrocatalysts for oxygen reduction reaction(ORR) is of importance for fuel cells and metal-air batteries. Herein, three-dimensional nitrogen and phosphorous co-doped graphene aerogel(NPGA) was prepared via the pyrolysis of polyaniline(PANi) coated graphene oxide aerogel synthesized by oxidative polymerization of aniline on graphene oxide(GO) sheets in the presence of phytic acid. The uniform coating of PANi thin layer on the surface of GO sheets enables the formation of highly porous composite aerogel of PANi and GO. The subsequent thermal treatment is able to prepare the porous NPGA due to the carbonization of PANi and phytic acid as nitrogen and phosphorous resources. When used as electrocatalysts,the as-prepared NPGA electrocatalysts exhibited good catalytic activity to ORR via an efficient four-electron pathway with good stability, benefiting from the highly porous structure and the heteroatom co-doping. More importantly, Zn-air batteries operated in ambient air have been fabricated by coupling a Zn plate with the NPGA electrocatalyst in an air electrode, demonstrating the maximal power density as high as ~260 W/g and a good long-term stability with slightly potential decay for over 450 h. The facile method for preparing efficient carbon based ORR electrocatalysts would generate other potential applications including fuel cells and others.

Inverted polymer solar cells with a solution-processed zinc oxide thin film as an electron collection layer

A solution-processed zinc oxide (ZnO) thin film as an electron collection layer for polymer solar cells (PSCs) with an inverted device structure was investigated. Power conversion efficiencies (PCEs) of PSCs made with a blend of poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl C61-butyric acid methyl ester (PCBM) are 3.50% and 1.21% for PSCs with and without the ZnO thin film, respectively. Light intensity dependence of the photocurrent and the capacitance-voltage measurement demonstrate that the increased PCEs are due to the restriction of the strong bimolecular recombination in the interface when a thin ZnO layer is inserted between the polymer active layer and the ITO electrode. These results demonstrate that the ZnO thin film plays an important role in the performance of PSCs with an inverted device structure.

ZnO hierarchical aggregates： Solvothermal synthesis and application in dye-sensitized solar cells

ZnO hierarchical aggregates have been successfully synthesized by solvothermal methods through reaction of zinc acetate and potassium hydroxide in methanol solution. The shapes of the aggregates were controlled by varying the ratio of Zn2~ and OH- ions in the reaction system, while the size can be tuned from 2μm to 100 nm. Oriented attachment was found to be the main mechanism of the three-dimensional assembly of small ZnO nanocrystallites into large aggregates. The performance of these aggregates in dye-sensitized solar cells （DSCs） indicated that hierarchical structured photoelectrodes can increase energy conversion efficiency of DSCs effectively when the sizes of aggregates match the wavelengths of visible light.