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Covalent organic frameworks (COFs) possess extraordinary porosity, structural diversity, and good electrochemical performance, and have broad application prospects in the field of energy storage. However, the low conductivity of COFs limits its further development. In this paper, the electrochemical performance of triphenylamine-based COFs (TPA-COFs) was improved by compounding with highly conductive polyaniline (PANI) using solvothermal synthesis process. The highly conductive polyaniline fibers can act as conductive path in the composite to accelerate the charge transfer rate of TPA-COFs. The π-π interaction between TPA-COFs and PANI effectively decreases the agglomeration degree of PANI. The good dispersion of composite results in that the specific surface area of TPA-COFs/PANI-20 is high as 1233.9 m2 g−1, which provides rich diffusion channels for electrolyte ions. Moreover, the strong π-π structure in the composites ensures the stability of the material skeleton. Thus, TPA-COFs/PANI composite exhibits excellent rate characteristics and cycling stability. more...

Free-standing flexible supercapacitive electrodes have practical application for wearable energy storage devices. In this paper, graphene paper (GP), a flexible electrode substrate, was prepared by one-step reduction of graphene oxide (GO) using HI solution. GP can be used independently as a flexible electrode with specific capacitance of 227 F/g. In order to make up for the shortage of GP specific capacitance storage, polyaniline (PANI) with high specific capacitance and good electrical conductivity was selected to composite with GP by electrochemical polymerization approach. This method to fabricate electrode material by direct electrochemical polymerization avoids the use of conductive binder and organic solvent. Owing to the specific capacitance contribution of PANI and GP, the PANI/GP composites exhibit higher specific capacitance when the polymerization time is 30 s and the polymerization voltage is 0.8 V. At 1 A/g current density, the specific capacitance of composite is up to 759 F/g, which is 3.34 times of neat GP. more...

A Poly (3, 4-dioxyethylthiophene)–Carbon Nanotubes (PEDOT–CNT) composite electrochromic material, connected by interfacial covalent bonds, was successfully synthesized by electrochemical copolymerization of 3, 4-dioxyethylthiophene with thiophene-2-methylamine functionalized CNT. The molecular and aggregate structures of PEDOT–CNT were investigated by Fourier transform infrared spectroscopy, Raman spectroscopy, scanning electron microscopy and transmission electron microscopy. The electrochemical behavior and electrochromic properties of PEDOT–CNT were measured by CV (cyclic voltammetry), UV–Vis (ultraviolet visible spectroscopy) and EIS (electrochemical impedance spectroscopy). The test results show that the electrochromic performance of PEDOT–CNT is better than that of neat PEDOT. As the percentage of carbon nanotubes increases, the contrast and response speed of the composites increase accordingly. The PEDOT film has a contrast under square-wave potential of 0.54, a coloring time of 6.42 s, and a fading time of 2.54 s. Compared with PEDOT, the contrasts of PEDOT–CNT-3%, PEDOT–CNT-5% and PEDOT–CNT-7% are increased by 31%, 33%, and 89%, respectively. The response speeds of PEDOT–CNT-5% increase to coloring time of 3.51 s and fading time of 1.37 s. more...

Polyaniline nanotubes (PANI-T) and graphene oxide (GO) have been compounded by a postcomposition method with the assistance of electrostatic adsorption. Using this so-called postcomposition method, both the electric double-layer capacitance of the GO and the pseudocapacitance of the conducting polymer can be utilized. PANI-T prepared by a rapid mixing method was positively charged by pretreatment with (3-aminopropyl)triethoxysilane (APTES). PANI/GO composites were obtained by mixing the positively charged PANI-T and negatively charge GO with the assistance of electrostatic attraction. Charge–discharge measurements in 1 mol L−1 H2SO4 aqueous electrolyte revealed that the specific capacitance of PANI-T/GO-10% could reach 1220 F g−1 at a current density of 0.5 A g−1, being much higher than the value of 648 F g−1 for PANI-T. After 500 cycles of charge–discharge testing, the composite retained 97% of its capacitance. These enhanced supercapacitive properties can be attributed to the two types of energy storage mechanism and the electrostatic interaction between GO and PANI-T. Preparation of such PANI-T/GO composite electrode materials by electrostatic adsorption thus provides an efficient approach for improvement of the supercapacitive properties of conducting polymers or metal oxides. more...

Multiferroic YFeO3 nanofibers were prepared by electrospinning. The as-prepared nanofibers were characterized by XRD, TG-DTA, SEM and Raman spectrum. The magnetic property and photocatalytic activi... more...

In this paper, water-dispersible and covalently bonded polyaniline-carbon nanostructures, including polyaniline-reduced graphene oxide (PANI-rGO), polyaniline-single-walled carbon nanotubes (PANI-SWCNTs), and polyaniline-reduced graphene oxide/single-walled carbon nanotube (PANI-rGO/SWCNTs) nanocomposites, were synthesized by grafting PANI onto p-phenylenediamine (PPD)-functionalized graphene oxide (GO) or single-walled carbon nanotubes (SWCNTs) using polystyrene sulfonate (PSS) as a macromolecular dopant agent. The structures and morphologies of the PANI, PANI-rGO, PANI-SWCNTs, and PANI-rGO/SWCNTs nanocomposites were characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. The cyclic voltammetry and UV–vis spectra were performed on an electrochemical workstation and a UV–vis spectrometer, respectively. The results show that the electrochromic and electrochemical properties of nanocomposites can benefit from the high conductivity of SWCNTs and the abundant active sites of rGO. When SWCNTs and rGO work together, their respective shortcomings are overcome, allowing the nanocomposite to exhibit the best electrochemical and electrochromic properties. The optical contrast increased from 0.38 for PANI to 0.52 for PANI-rGO/SWCNTs. The coloring and bleaching times decreased from 2.59 s and 2.39 s, respectively, for PANI to 1.33 and 0.78 s, respectively, for PANI-rGO/SWCNTs. The charge transfer resistance (Rct) decreased from 135 Ω for PANI to 30 Ω for PANI-rGO/SWCNTs. The synergistic effect of PANI, rGO, and SWCNTs can significantly improve the electrochromic ability of PANI. Electrochromic properties of covalently bonded polyaniline-reduced graphene oxide/single walled carbon nanotubes nanocomposites. A high performance electrochromic material was prepared using polyaniline (PANI) and two different dimensional carbon nanostructures, single-walled carbon nanotubes (SWCNTs) and reduced graphene oxide (rGO) as the components. The covalent bond was introduced to interface between PANI and two carbon nanostructures to form a three-dimensional conductive network. Owing to the high electron conduction through directly connected covalent bond and loose molecular chain aggregation brought by two various dimensional carbon nanostructure, PANI-rGO/SWCNTs nanocomposites exhibit superior electrochemical and electrochromic properties (high optical contrast and short switching time) compared with PANI. more...

In this study, polyaniline (PANI) nanostructures with different morphologies (nanofibers, nanotubes, and nanospheres) were obtained via interfacial polymerization, rapid mixing reaction, and hydrothermal method. The influences of the synthesis methods on the morphologies and supercapacitive properties of PANI nanostructures were investigated. The chemical structures of materials were characterized by Fourier-transform infrared and Raman spectroscopies. Scanning electron microscopy and transmission electron microscopy images were used to explore the morphologies of PANI nanostructures. N2 adsorption–desorption isotherm, cyclic voltammetry, charge–discharge test, and electrochemical impedance spectroscopy were used to characterize the pore distribution, electrochemical, and supercapacitive properties of PANI nanostructures. The results show that PANI nanotubes (PANI-T) exhibit the best electrochemical performances among three kinds of PANI nanostructures. The PANI-T exhibits high specific capacitances of 648 and 290 F g−1 at current densities of 0.5 and 10 A g−1, respectively, indicating its good supercapacitive property and rate capability. The enhanced electrochemical and supercapacitive performances can be attributed to its hollow nanotube structure. more...

In this article, a high specific capacitance biomass carbon/MnO2 nanocomposites electrode materials were prepared by hydrothermal method. The porous sugarcane bagasse based biomass carbon was used as the host to load MnO2 nanospheres. The final obtained nanocomposites exhibit high specific capacitance. Besides, the effects of different electrolytes on the electrochemical properties of sugarcane bagasse carbon (SBC)/MnO2 nanosphere composites (SBC/MnO2) were also investigated. In comparison with MnO2 nanospheres, the specific capacitances of the SBC/MnO2 composite materials are improved whether in alkaline electrolyte or neutral electrolyte. Especially, in 1 M Na2SO4 electrolyte, the specific capacitance of SBC/MnO2 composite is up to 747 F·g−1 at a current density of 1 A·g−1, which is much higher than the MnO2 nanospheres at the same current density. At the same time, after 1000 cycles of charge–discharge process in a neutral electrolyte, the specific capacitance retention of SBC/MnO2 composite reaches 77%. more...

In this article, polyaniline nanofibers (PANI-NF)/manganese dioxide composites (PANI/MnO2) were synthesized through an interfacial polymerization approach. The PANI-NF and MnO2 were obtained by in situ oxidation of aniline by potassium permanganate and in situ reduction of potassium permanganate by aniline, respectively. During the interfacial polymerization, the monomer aniline can only be oxidized to PANI after it diffuses into the water phase. This diffusion-control feeding process of the monomer results in nanofiber structure. The morphologies and crystal structures of the prepared PANI/MnO2 composites were measured by scanning electron microscopy and x-ray diffraction. The supercapacitive behaviours of these composites were analysed by cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) tests. The CV and GCD tests indicate that the PANI/MnO2 composites possess better electrochemical activity and higher capacitive properties compared to neat PANI nanofibers. The specific capacitance of PANI/MnO2 composites and PANI-NF are 751 F g−1 and 180 F g−1 at 0.2 A g−1 in Na2SO4 solution, respectively. We believe that the enhanced capacitive properties are related to the special nanostructure and strong interaction between PANI and MnO2 that resulted from the interfacial synthesis method. more...

Polyaniline nanowires (PANI NWs) were synthesized under different temperatures through a facile hydrothermal method and used as electrodes for high-performance pseudocapacitor. The resulting samples were analyzed by X-ray diffraction, Fourier transform infrared spectroscopy, Raman spectroscopy, scanning electron micrographs, thermogravimetric analysis, and X-ray photoelectron spectroscopy. Electrochemical properties of these PANI electrodes are studied by cyclic voltammetry, galvanostatic charge–discharge test, and electrochemical impedance spectroscopy in 0.5M H2SO4 aqueous solution. The highest specific capacitance is obtained on the PANI NWs synthesized under 80°C (PANI-80) with 540.0 F g−1 at current density of 0.5 A g−1 accompanied with 82% specific capacitance retention after 1000 charge discharge cycles at 5 A g−1 current density. more...

In this article, polyaniline nanofibers/reduced graphene oxide (PANI-NFs/rGO) nanocomposites were prepared by a one-pot hydrothermal method. Under the condition of high temperature and high pressure, graphene oxide (GO) was reduced to rGO and aniline was in-situ polymerized to form PANI-NFs using ammonium persulfate as oxidant. The morphologies and structures of PANI-NFs/rGO nanocomposites were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy (FTIR), and Raman analysis. The results show that PANI-NFs uniformly grow on the surfaces of rGO sheets, which can act as spacers to prevent the aggregation of rGO. Combining with FTIR and Raman analysis, it can be concluded that PANI-NFs/rGO nanocomposites are successfully prepared. The electrochemical performances of PANI-NFs/rGO nanocomposites were tested by cyclic voltammetry and galvanostatic charge–discharge. The PANI-NFs/rGO nanocomposites exhibit superior electrochemical performances compared to the PANI-NFs. With 10 wt% of GO loaded, the PANI-NFs/rGO nanocomposite exhibits highest specific capacitance of 942 F g−1 at a current density of 1 A g−1. The PANI-NFs/rGO nanocomposites also demonstrate good rate capacity and high cycling stability under the high discharging current density (10 A g−1), the specific capacitance can still reach to 680 F g−1. After 1000 charge–discharge cycling at a current density of 5 A g−1, 78% of specific capacitance can be retained. The enhanced capacitive performances can be attributed to the facile electron conduction pathway brought by the even distribution of highly conductive rGO nanosheets. more...

Polyaniline is one of the most common electrode materials for supercapacitors. The morphology of polyaniline directly affects the properties of polyaniline. In this paper, a new method for preparing hollow polyaniline nanospheres is described. Polyaniline-S with solid and hollow structures are successfully synthesized by the hydrothermal method, through varying the amounts of the catalyst and oxidant. The prepared hollow nanospheres have uniform particle size, a smooth surface, and uniform wall thickness. The hollow structure provides rapid permeability to the material, facilitating the transfer and transport of charges and ions in the electrolyte, and it can also act as an ion storage tank to increase the accumulation of ions inside. The specific capacitance of polyaniline-S is high at 235 F g-1 at 0.5 A g-1. To reduce the aggregation of polyaniline-S and improve the electrochemical activity, polyaniline-S, and graphene oxide are composited using the interfacial electrostatic interaction. The content of graphene oxide has a significant influence on the electrochemical performance of the composites. The specific capacitance of the polyaniline-S/ graphene oxide composite with a 10% loading amount of graphene oxide reaches 535 F g-1 at 0.5 A g-1, increase of nearly 128% compared to representing a significant polyaniline-S. The specific capacitance retention rate is 93.6% after 10,000 cycles. more...

NiCo-based bimetal-organic frameworks (NiCo-MOF) are synthesized via a hydrothermal approach, using 4,4′-biphenyldicarboxylic acid (BPDC) as a ligand. Structural characterizations find that NiCo-MOF is composed of one-dimensional micro-nanorods and regular three-dimensional cuboids assembled by one-dimensional micro-nanorods，possessing a good crystalline structure, in which nickel and cobalt ions have been coordinated to the BPDC ligands. Moreover, NiCo-MOF can be stable below 300 °C in air. The electrochemical measurements show that GCD activation at a high current density can significantly increase the capacity of NiCo-MOF due to decreasing the charge-transfer resistance and ion diffusion impendence. The specific capacitance of NiCo-MOF reaches 990.7 F/g from 156.5 F/g at 1 A/g, and the coulombic efficiency increases to 98.0% from 77.6% after the CV-GCD activation. Activated NiCo-MOF exhibits prominent pseudocapacitive behaviors, high specific capacitances at different current densities and a good cycling stability after 1000 cycles. The capacity of NiCo-MOF is up to 405.0 F/g when the current density increases to 20 A/g, and remains 553.2 F/g at 1 A/g after 3000 cycles. Compared with monometallic Ni-MOF and Co-MOF, bimetallic NiCo-MOF possesses a much higher capacity at different current densities due to the lower intrinsic resistance, charge-transfer resistance and ion diffusion impendence. more...

In this article, we reported a biomass carbon/MnO2 nanocomposite electrode material prepared by a hydrothermal method. Sugarcane bagasse and KOH were the carbon source and activation agent, respectively. The obtained sugarcane bagasse carbon is rich in pore structure, so it can act as the host for MnO2. The biomass carbon/MnO2 nanocomposite electrode was prepared by a hydrothermal method. The morphologies of materials were observed by scanning electron microscopy. Raman spectra and x-ray diffraction were utilized to characterize the molecular and crystal structures of samples, respectively. The electrochemical and capacitive performances of materials were tested by electrochemical workstation. By calculation, the specific capacitance of sugarcane bagasse carbon, MnO2 and composite electrode are 280 F g−1, 163 F g−1 and 359 F g−1, respectively. Compared with pure sugarcane bagasse carbon and MnO2, the specific capacitance of the composite increases by 28% and 120%, respectively. After 2000 cycles of charge and discharge, the capacitance retention of the composite is 94%, which is higher than 91% of sugarcane bagasse carbon and 45% of MnO2. more...

A novel ferrocene-containing hybrid electrochromic material was synthesized via copolymerization of aniline with p-phenylenediamine functionalized acetyl ferrocene in the presence of poly (styrene sulfonate) dopant in an aqueous medium, and neat polyaniline (PANI) was prepared for comparison. The polymerization characteristics and the structure of the copolymer were systematically studied by Fourier-transform infrared, meanwhile, their electrochromic properties and electrochemical behaviors were tested by UV–vis spectra, cyclic voltammetry and electrochemical impedance spectroscopy (EIS). It was found that the strong covalent bond and large conjugated system between PANI and ferrocene enhance the electron transfer rate and electron delocalization in the ferrocene-polyaniline (Fc-PANI) hybrid. In particular, the electrochromic device with Fc-PANI as the active layer shows significant enhancement in optical contrast over the PANI-based device. more...

In this paper, we designed a novel organic-inorganic nanohybrid electrochromic material through tethering polyaniline and gold colloids with an interfacial coordinate bond. The enhanced electrochemical and electrochromic properties were expected owing to the high conductivities of the gold colloids and strong interfacial interaction between the organic phase and inorganic phase. The water-dispersible polyaniline-gold (PANI-Au) nanohybrids were synthesized successfully through grafting copolymerization of aniline with p-aminothiophenol (PATP) functionalized gold colloids in an aqueous system using a macromolecular acid, poly(styrene sulfonate) (PSS) as the dopant agent. The structures, morphologies, and electrochemical and electrochromic properties of PANI-Au nanohybrids were characterized by the UV–vis, FTIR, Raman spectrometers, SEM, and electrochemical working station, respectively. The results show that through incorporating gold nanoparticles into the PANI matrix with the interfacial coordinate bond, PANI-Au nanohybrids possess uniform nanoparticles morphologies with diameter ~180 nm. The electrochemical activity and the charge transfer process of PANI were enhanced, which is proved by the CV test and EIS analysis. As the results, the PANI-Au nanohybrids can switch at relatively lower potentials and give a higher optical contrast as comparison with neat PANI: PSS. With ~1.4 wt% Au loading amount, the contrast of PANI-Au nanohybrid is 0.97, which is much higher than 0.76 of PANI: PSS. The coloration and bleaching time are also shortened from 13.4 s and 8.9 s for PANI: PSS to 8.3 s and 7.6 s for PANI-Au-c, respectively. more...

Inspired by hydrothermal synthesis of inorganic crystallites, we apply one-step hydrothermal polymerization to directly grow polyaniline on fluorine-doped tin oxide (FTO) substrate. In contrast to classical procedure that requires long reaction times and low temperature, hydrothermal polymerization allows for only 3 h under hydrothermal condition. Investigation of the morphology via SEM suggests that PANI fiber aggregates uniformly on FTO substrate. The PANI film was used as electrochromic layer in an electrochromic device and the obtained PANI film shows high electrochromic performance. We believe that this study provided a novel way to directly grow PANI on FTO substrate and, thus, has some impact on the applications of other conjugated polymers in electrochromic and electrochemical devices. more...

Two-dimension covalent organic frameworks (2D COFs) are porous materials with the interlayer π-π interaction and excellent optoelectronic properties. Their adjustable porous structure and designable molecular structure endow them unlimited possibilities in the field of optoelectronic materials and other functional materials. In this paper, 2D COF electrochromic films were prepared by solvothermal synthesis method with different amounts of functionalized carbon nanotubes (FCNT) loading to improve their conductivity. The morphology characterization of COFDAAQ-TFP reveals its intertwined nanofiber structure. The electrochromic performance of COFDAAQ-TFP film shows that the color of COFDAAQ-TFP and FCNT-COFDAAQ-TFP have a reversible transformation from orange to dark brown during the redox process. When the loading amount of FCNT is 1%, FCNT-COFDAAQ-TFP exhibits best electrochromic properties, which has a contrast of 0.358 and coloring time of 5.7 s. Relative to COFs, FCNT-COF has enhanced contrast and stability, which is a potential electrochromic material in many fields such as smart window and smartphone back case. more...

In this study, we fabricated hexagonal YFeO3 films on Si(100) and Si(111) substrates by a sol-gel method, and investigated the effect of substrate orientation on the structural, ferroelectric and piezoelectric properties of the YFeO3 films. Grazing incidence X-ray diffraction reveals that the YFeO3 films on Si(100) and Si(111) have slight preferred-orientation in (110) and (004) direction, respectively. Both films possess granular microstructure with good crystallization, as well as low surface roughness. The (004)-oriented film has higher density than the (110)-oriented film, resulting in lower leakage current. The two films show weak ferroelectric properties and different domain structures. Local amplitude and phase response loops manifest that the film on Si(111) possesses larger phase change and coercive field. While influenced by polarization rotation towards the applied field direction, larger effective piezoelectric coefficient d33 of 67 pm/V has been found in the film on Si(100). These findings suggest that preferred orientation can account for the physical properties of multiferroic YFeO3 films. more...

Conjugated covalent organic frameworks (COFs) with redox properties can be considered as conductive polymers with ordered porous structures and can be designed for photoelectric materials application. In this paper, 2,6-diaminoanthraquinone and 1,3,5-triformylresorcinol (DAAQ-TFP) COF with anthraquinone active unit was synthesized by solvothermal method for electrochromic application in a Teflon-lined autoclave. Functionalized graphene oxide (FGO) was covalently bonded with COF to improve its electrical conductivity and photoelectric properties. After the addition of FGO, the impedance of COF was reduced, and the optical contrast and cyclic stability of COF were increased. At potential windows of 2.5 V to -3.8V, the COF-FGO-2% can be switched reversible from orange to dark brown. Stability test shows that the contrast retention is 109.1% after 1800s switching, which is much higher than COF (75%). Considering the abundance of COF building units with redox activity available, it is possible to develop novel COF based electrochromic materials with rich colors. more...

The molecular architecture of conducting polymers has a significant impact on their conjugated structure and electrochemical properties. We have investigated the influence of star-shaped structure on the electrochemical and electrochromic properties of polyaniline (PANI). Star-shaped PANI (SPANI) was prepared by copolymerization of aniline with triphenylamine (TPA) using an emulsion polymerization method. With addition of less than 4.0 mol.% TPA, the resulting SPANI exhibited good solubility in xylene with dodecylbenzenesulfonic acid (DBSA) as doping acid. The structure and thermal stability of the SPANI were characterized using Fourier-transform infrared spectroscopy, Raman spectroscopy, and thermogravimetric analysis, and the electrochemical behavior was analyzed by cyclic voltammetry (CV). The electrochromic properties of SPANI were tested using an electrochemical workstation combined with an ultraviolet–visible (UV–Vis) spectrometer. The results show that, with increasing TPA loading, the thermal stability of SPANI increased. With addition of 4.0 mol.% TPA, the weight loss of SPANI was 36.9% at 700°C, much lower than the value of 71.2% for PANI at the same temperature. The low oxidation potential and large enclosed area of the CV curves indicate that SPANI possesses higher electrochemical activity than PANI. Enhanced electrochromic properties including higher optical contrast and better electrochromic stability of SPANI were also obtained. SPANI with 1.6 mol.% TPA loading exhibited the highest optical contrast of 0.71, higher than the values of 0.58 for PANI, 0.66 for SPANI-0.4%, or 0.63 for SPANI-4.0%. Overdosing of TPA resulted in slow switching speed due to slow ion transport in short branched chains of star-shaped PANI electrochromic material. Long-term stability testing confirmed that all the SPANI-based devices exhibited better stability than the PANI-based device. more...

In this paper, we demonstrate a simple approach to improve the electrochromic performances of polyaniline (PANI) by incorporating PANI nanofibers (PANI-NFs) synthesized by interfacial polymerization into water-soluble PANI:poly(styrene sulfonate) (PANI:PSS). The one-dimensional PANI-NFs endow spin-coated PANI film high electrochemical activities and electrochromic properties. The structures and morphologies of PANI-NFs were characterized by FTIR spectroscopy and SEM observation. The electrochemical behaviors of PANI/PANI-NFs composites were analyzed by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The electrochromic properties of composites were tested using electrochemical working station combining a UV-Vis spectrometer. The results show that the PANI-NFs with even diameter of ~ 30 nm can be synthesized easily using interfacial polymerization method. With the increasing of feeding amount of PANI-NFs, the oxidation peaks of CV curves shift to low potential direction, indicating enhanced electrochemical activities. The electrochromic test confirms that the PANI/PANI-NFs composites films have higher electrochromic contrast of 0.67 as comparison to 0.49 of PANI:PSS film. The PANI/PANI-NFs also exhibit excellent electrochromic stability. After 2000 cycles switching, only less than 4% contrast decay is observed. The enhanced electrochromic properties can be attributed to the small charge-transfer resistance and facile ion diffusion process brought by PANI-NFs. The EIS tests exhibit that with incorporating of highly conductive PANI-NFs, the PANI/PANI-NFs composites possess relatively lower charge-transfer resistance of 76 Ω as comparison to 94 Ω of neat PANI:PSS. more...

Electrochromic properties of organic or inorganic materials can be improved through preparing organic/inorganic electrochromic nanocomposites. In electrochromic nanocomposites, the interfacial interactions between the organic and inorganic phases play three important roles in preparation and application of the nanocomposites. Firstly, the interfacial interactions result in stable molecular structures. Secondly, they also improve the electron conduction and ion transport process in the nanocomposites. Thirdly, they enhance the electrochemical and electrochromic properties of the nanocomposites. In this paper, we review the common interfacial interactions including covalent bond, coordination bond, electrostatic interaction, hydrogen bond and π-π stacking interaction between the organic and inorganic phases in the electrochromic nanocomposites. The preparation method, the relationship between the structure and properties, and the mechanism of modulation of electrochromic effect in the nanocomposites with various interfacial interactions are surveyed. The strong interfacial interaction, e.g., covalent bond, is helpful for obtaining electrochromic nanocomposites with high electron conduction and high structural strength. However it is very complicated to construct covalent bond between the organic and inorganic phases. Another strong interfacial interaction, the coordination bond is mainly confined to preparation of electrochromic complex of metal ion and pyridine derivative. While, the weak interfacial interactions, e.g., electrostatic interaction, hydrogen bond and π-π stacking interaction, exist widely between the organic and inorganic phases in the electrochromic nanocomposites. Relative to single strong interaction, the multiple weak interactions may be a development direction for achieving high performance electrochromic effect in the organic/inorganic nanocomposites, owing to their integrated effect and various adjusting mechanisms of electrochromic properties. more...

Tungsten trioxide (WO3) thin films are of great interest as counter electrodes in electrochromic (EC) devices such as ‘smart window’ for energy-efficient buildings. Uniform WO3 nanoplates filmed as EC working electrodes were fabricated on seed-free fluorine-tin-oxide (FTO) coated glass via a facile and addictive agent-free hydrothermal process. The WO3 nanoplates were characterised by scanning electron microscopy and the X-ray photoelectron spectroscopy. The morphological analysis of the film showed that the WO3 nanoplates lying on the FTO glass uniformly. Fourier transform infrared spectroscopy was applied to study the vibrational information of the sample. Furthermore, uniform WO3 nanoplates exhibit well performance of EC properties. Owing to the highly two-dimensional nanostructure, a fast switching speed of 12 and 3 s for colouration and bleaching are achieved for WO3 film. These properties of the WO3 nanoplates film endow its promising practical applications in smart windows. more...

This paper demonstrates a simple and effective approach to fabricate highly crystalline poly(2,5-dimethoxyaniline) (PDMA) nanoplates using various organic sulfonic acids including Dodecyl benzenesulfonic acid (DBSA), Camphorsulfonic acid (CSA) and p-Toluenesulfonic Acid (p-TSA) as the dopant agents. The structures and morphologies of PDMA nanoplates were characterized using Fourier transform infrared spectrometer, Raman spectrometer, X-ray diffraction, Atom force microscope and Electron microscope. The results show that the PDMA nanoplates possess high crystallinity and layered nanoplate aggregation structure. The estimated degree of crystallinity is higher than 95 %. With different organic sulfonic acids used, the aggregation structures of PDMA nanoplates vary from triclinic hexahedron to cuboid and rod shape. Through adjusting the dopant agent/monomer molar ratio, the yield of PDMA nanoplates can be as high as 53 %. more...

In this paper, the covalently bonded polyaniline (PANI) nanofiber/multi-walled carbon nanotubes (MWCNT) composites were synthesized via interfacial polymerization of aniline with para-phenylenediamine functionalized MWCNT at the interface of oil/water system. Owing to the diffusion-controlled growth process of PANI, PANI with uniform fiber structure were obtained. The morphology analysis showed that the diameter of PANI nanofiber decreased with the increasing of MWCNT loading amount. Impedance analysis showed that the charge-transfer resistances of the composites were reduced also with the increasing of MWCNT loading amount. The decreasing of charge-transfer resistances and change of morphology resulted in enhanced capacitive properties. Electrochemical tests showed that the specific capacitance of PANI, PANI/MWCNT-10% and PANI/MWCNT-20% were 405, 641 and 764 F·g-1, respectively. As comparison with pure PANI nanofiber, the specific capacitance of the composites increased by 58% and 88.6%, respectively. more...

Covalent organic framework is a designable and versatile platform for preparation of various functional materials including conventional gas adsorption and separation materials, catalysis matrix, and photoelectric materials, etc. The covalent organic framework with redox building block and conjugated molecular structure can be viewed as a conjugated polymer with ordered porous structure. In this paper, we synthesized a Schiff base type conjugated organic framework (COF) by a solvothermal method in a common Teflon-lined stainless steel autoclave. The reversible reaction of dynamic imine bonds in solvothermal process induces the morphology transform of COF from nanoparticle to nanofiber. Besides of its structure, morphology, nanofiber-formation mechanism and electrochemical properties, the electrochromic properties of COF were investigated for the first time. Owing to the redox building block of triphenylamine, the COF possesses reversibly electrochromic behavior caused by reversibly redox reaction and band gap change of triphenylamine unit. Under step potentials between −2.5 V and 2.5 V, the COF can switch between bright yellow color and brown color. The stability test shows that the device can reversibly switch with stable contrast after slight decay at the initiated cycles. In consideration of abundant options of building units with redox feature, the COF based electrochromic materials with rich color and novel properties can be expected. more...

A facile synthesis method of poly(3,5-dimethoxyaniline) (P(3,5-DMA)) hollow microspheres was demonstrated by the interfacial polymerisation of 3,5-dimethoxyaniline (3,5-DMA) using camphorsulfonic acid (CSA) as the doping agent and soft template. The obtained P(3,5-DMA) hollow microspheres possess narrow size distribution and uniform shape. A possible growth mechanism of the hollow microspheres was proposed through studying the change in morphologies of P(3,5-DMA) at different reaction times. It is believed that the slow diffusion speed of monomer from the oil phase to the water phase in the interfacial polymerisation system controls the progress of polymerisation. Moreover, the interaction between amino group of the monomer and the sulfonic acid group of the doping agent micelle guides the formation of the hollow microspheres. more...

Orthorhombic YFeO3 thin film was prepared on La0.67Sr0.33MnO3/LaAlO3 substrate by a sol–gel spin-coating method. The structures of the YFeO3/La0.67Sr0.33MnO3/LaAlO3 (YFO/LSMO/LAO) sample were detected by x-ray diffraction pattern, Raman spectrometer, scanning electron microscopy, and atomic force microscope. The local ferroelectric polarization switching properties of the orthorhombic YFO film were confirmed by piezoresponse force microscopy (PFM) for the first time. The results show that the YFO film deposited on LSMO/LAO possesses orthorhombic structure, with ultra-fine crystal grains and flat surface. The leakage current of the YFO film is 8.39 × 10−4 A⋅cm−2 at 2 V, with its leakage mechanism found to be an ohmic behavior. PFM measurements indicate that the YFO film reveals weak ferroelectricity at room temperature and the local switching behavior of ferroelectric domains has been identified. By local poling experiment, polarization reversal in the orthorhombic YFO film at room temperature was further observed. more...