聚合物/无机纳米复合材料的发展及应用

本文介绍了近年来聚合物 /无机纳米复合材料的发展 ,对潜在的应用前景进行了总结 。

Effect of nanofibers at surface of carbon fibers on microstructure of carbon/carbon composites during chemical vapor infiltration

Before densification by chemical vapor infiltration,carbon or SiC nanofibers were grown on the surface of carbon fibers by catalytic chemical vapor deposition using electroplated Ni as catalyst.The modification and mechanism of nanofibers on the pyrocarbon deposition during chemical vapor infiltration were investigated.The results show that the nanofibers improve the surface activity of the carbon fibers and become active nucleation centers during chemical vapor infiltration.They can induce the ordered deposition of pyrocarbon and adjust the interface bonding between pyrocarbon and carbon fibers during the infiltration.

Effect of ammonia gas etching on growth of vertically aligned carbon nanotubes/nanofibers

The etching effect of ammonia （NH3） on the growth of vertically aligned nanotubes/nanofibers （CNTs） was investigated by direct-current plasma enhanced chemical vapor deposition （DC-PECVD）. NH3 gas etches Ni catalyst layer to form nanoscale islands while NH3 plasma etches the deposited amorphous carbon. Based on the etching effect of NH3 gas on Ni catalyst, the differences of growing bundles of CNTs and single strand CNTs were discussed; specifically, the amount of optimal NH3 gas etching is different between bundles of CNTs and single strand CNTs. In contrast to the CNT carpet growth, the single strand CNT growth requires shorter etching time （5 min） than large catalytic patterns （10 rain） since nano dots already form catalyst islands for CNT growth. Through removing the plasma pretreatment process, the damage from being exposed at high temperature substrate occurring during the plasma generation time is minimized. High resolution transmission electron microscopy （HTEM） shows fishbone structure of CNTs grown by PECVD.

Scalable production of self-supported WSe/CNFs by electrospinning as the anode for high-performance lithium-ion batteries

WS2/carbon nanofibers （WS2/CNFs） are obtained by a simple electrospinning method in which few-/ single-layer WS2 is uniformly embedded in carbon fibers. When used as the active anode material for Li-ion cells, these nanofibers exhibit a first-cycle discharge/charge capacity of 941/756 mAh/g at 100 mAJg and maintain a capacity of 458 mAh/g after 100 cycles at 1 A/g. The evolution of size and crystallinity of WS2 with heating treatment are system- atically studied, which are found to strongly influence the final electrochemical performance. Interestingly, the WS2 samples of lowest crystallinity show the highest performance among all studied samples, which could result from the large interfacial capacity for Li ions due to their large specific surface area. More interestingly, the inherent flexible attribute of electrospun nanofibers renders them a great potential in the utilization of binder-flee anodes. Similar high discharge/charge capacity of 761/604 mAh/g with a first coulombic efficiency of 79.4 % has been achieved in these binder-flee anodes. Considering the universal of such simple and scalable preparation strategy, it is very likely to extend this method to other similar two-dimensional layered materials besides WS2 and provides a promising candidate elec- trode for developing flexible battery devices.

Controlled Ag-driven superior rate-capability of Li4Ti5O12 anodes for lithium rechargeable batteries

The morphology and electronic structure of a Li4Ti5012 anode are known to determine its electrical and electrochemical properties in lithium rechargeable batteries. Ag-Li4Ti5012 nanofibers have been rationally designed and synthesized by an electrospinning technique to meet the requirements of one-dimensional （1D） morphology and superior electrical conductivity. Herein, we have found that the 1D Ag-Li4Ti5012 nanofibers show enhanced specific capacity, rate capability, and cycling stability compared to bare Li4Ti5012 nanofibers, due to the Ag nanoparticles （〈5 nm）, which are mainly distributed at interfaces between Li4Ti5O12 primary particles. This structural morphology gives rise to 20% higher rate capability than bare Li4Ti5O12 nanofibers by facilitating the charge transfer kinetics. Our findings provide an effective way to improve the electrochemical performance of Li4Ti5O12 anodes for lithium rechargeable batteries.

One-pot synthesis of Li_3VO_4@C nanofibers by electrospinning with enhanced electrochemical performance for lithium-ion batteries

Electrospinning is firstly used to one-pot synthesis of Li3VO4@C nanofibers in a large scale. Although with the presence of organic sources in synthesis process, the pure phase Li3VO4 with superior nanofibrous morphology is still successfully obtained through adjusting different heat treatment processes and different vanadium sources. The prepared Li3VO4@C nanofibers exhibit a unique structure in which nanosized Li3VO4 particles are uniformly embedded in amorphous carbon matrix. Compared with LiBVO4/C powder, Li3VO4@C nanofibers display enhanced reversible capacity of 451 mAhg^-1 at 40mAg^-1 with an increased initial coulombic efficiency of 82.3%, and the capacity can remain at 394 mAh g ^-1 after 100 cycles. This superior electrochemical performance can be attributed to its unique structure which ensures a high reactivity by nanosized Li3VO4, more stable electrode/electrolyte interface by carbon encapsulation, improved electronic conductivity and buffered volume changes by flexible carbon matrix. The electrospinning technology provides an effective method to obtain high performance Li3VO4 as a promising anode material for lithium-ion batteries.

Recyclable nanocellulose-confined palladium nanoparticles with enhanced room-temperature catalytic activity and chemoselectivity

We describe the synthesis of even-dispersed palladium nanoparticles(Pd NPs)confined within a cellulose nanofiber(CNF)matrix for developing a high-performance and recyclable catalyst.The CNF matrix was composed of CNF-assembled mesoporous nanosheets and appeared as soft and hydrophilic foam.Ultrafine Pd NPs(∼6 nm)with high-loading(9.6 wt%)were in situ grown on these mesoporous nanosheets,and their dense spatial distributions were likely to generate nano-confinement catalytic effects on the reactants.Consequently,the CNF-confined Pd NPs(CNF-Pd)exhibited an enhanced room-temperature catalytic activity on the model reaction of 4-nitrophenol hydrogenation with a highest rate constant of 8.8×10^−3 s^−1 and turnover frequency of 2640 h The CNF Pd catalyst possessed good chemical stability and recyclability in aqueous media which could be reused for at least six cycles without losing activity.Moreover,chemoselective reduction of 3 nitrostyrene was achieved with high yield(80%–98%)of 3-aminostyrene in alcohol/water cosolvent.Overall,this work demonstrates a positive nanoconfinement effect of CNFs for developing stable and recyclable metal NP catalysts.