Pseudocapacitive effects of multi-walled carbon nanotubes-functionalised spinel copper manganese oxide

Spinel copper manganese oxide nanoparticles combined with acid-treated multi-walled carbon nanotubes (CuMn2O4/MWCNTs) were used in the development of electrodes for pseudocapacitor applications. The CuMn2O4/MWCNTs preparation involved initial synthesis of Mn3O4 and CuMn2O4 precursors followed by an energy efficient reflux growthmethod for the CuMn2O4/MWCNTs. The CuMn2O4/MWCNTs in a three-electrode cell assembly and in 3 M LiOH aqueous electrolyte exhibited a specific capacitance of 1652.91 F g1 at 0.5 A g1 current load. Similar investigation in 3 M KOH aqueous electrolyte delivered a specific capacitance of 653.41 F g1 at 0.5 A g1 current load. Stability studies showed that after 6000 cycles, the CuMn2O4/MWCNTs electrode exhibited a higher capacitance retention (88%) in LiOH than in KOH (64%)

High power asymmetric supercapacitor based on activated carbon/reduced graphene oxide electrode system

We synthesized Graphene oxide (GO) using the modified Hummers method and further reduced to reduced graphene oxide (rGO) using hydrazine monohydrate and ammonia solution. The prepared materials were interrogated using different characterization techniques to determine which of them is more suitable for supercapacitor application. High resolution scanning electron microscopy (HRSEM) revealed a sheet-like morphology of separated thin sheets and wrinkled edges for GO, whereas rGO consist of thinner sheets with smaller pores than GO. The structural studies as elucidated from X-ray diffraction (XRD) shows that the GO has more interlayer spacing due to a higher oxygen content as compared to the rGO. The oxygen containing functional groups seen in GO either disappear or are greatly reduced in intensity in rGO as evidenced from the Fourier transform infrared spectroscopy (FTIR) of the materials. The electrochemical studies indicate that the rGO gave a higher current response compared to GO and a specific capacitance of 105.3 and 56.7 F g 1 respectively was delivered by rGO and GO at a scan rate of 10 mV s 1 in a three-electrode set-up. Asymmetric supercapacitor cells using GO and rGO as positive electrodes and activated carbon as the negative electrodes gave the highest specific capacitance value of 94.3 F g 1 for the AC//rGO cell and 59.6 F g 1 for the AC//GO cell at a current load of 0.25 A g 1. The specific capacitance obtained from the AC//rGO is comparable to most recorded values for rGO electrodes. A high specific power of 6411.7 W kg 1 was obtained at a specific energy of 22.6 W h kg 1 while at a specific energy of 25.7 W h kg 1, a specific power of 700.1 W kg 1 was obtained for the AC//rGO. This is due to the more porous and thinner sheet of the rGO. The overall results showed that the rGO gave better supercapacitive properties than the GO

Novel heterojunction superstrate Cu2ZnInS4−x (CZIS) thin film kesterite solar cell with vertical arrays of hexagonal ZnO nanorods window layer

Quaternary Cu2ZnInS4−x (CZIS) thin films have been prepared by a facile and cheap sol-gel spin coating technique. Low-temperature solution-based methods were used to fabricate a heterojunction solar cell in the superstrate architecture with CZIS thin film as the absorber, vertically aligned ZnO nanorod arrays, and CdS as the window and buffer layers respectively. ZnO nanorod arrays were prepared by hydrothermal technique and nanocrystal layer deposition technique were employed for the deposition of CdS-coated ZnO nanorod arrays. CZIS absorber layer was spin coated on the CdS-coated ZnO nanorod arrays and annealed at different temperatures. The vertically aligned ZnO nanorod arrays, and uniformly distributed CdS shell layer were confirmed from morphological studies. The device had a final configuration of Glass/ITO/ZnO NRs/CdS/ CZIS/Ag. HRSEM revealed a nanoflake-like morphology and a band gap between 1.5 and 1.77 eV for the CZIS thin films. CZIS superstrate solar cell had a power conversion efficiency of ∼ 0.61%, an open circuit voltage of ∼ 0.8 V, a short circuit current of ∼ 0.95 mA cm−2 and a fill factor of ∼ 61.35%. This method demonstrates a novel, facile and eco-friendly technique for synthesizing nanocrystalline CZIS thin films with promising photo response from the fabricated device indicating a proof of principle that this material can find application in solar cells.University of the Western Cap

Development of high performance composite lithium ion battery cathode systems with carbon nanotubes functionalised with bimetallic inorganic nanocrystal alloys

Philosophiae Doctor - PhDLithium ion cathode systems based on composites of lithium iron phosphate (LiFePO₄), iron-cobalt-derivatised carbon nanotubes (FeCo-CNT) and polyaniline (PA) nanomaterials were developed. The FeCo-functionalised CNTs were obtained through in-situ reductive precipitation of iron (II) sulfate heptahydrate (FeSO₄.7H₂O) and cobalt (II) chloride hexahydrate (CoCl₂.6H₂O) within a CNT suspension via sodium borohydrate (NaBH₄) reduction protocol. Results from high Resolution Transmission Electron Microscopy (HRTEM) and Scanning Electron Microscopy (SEM) showed the successful attachment FeCo nanoclusters at the ends and walls of the CNTs. The nanoclusters provided viable routes for the facile transfer of electrons during lithium ion deinsertion/insertion in the 3-D nanonetwork formed between the CNTs and adjacent LiFePO₄ particles

Photoluminescence quenching of a novel electroconductive poly(Propylene thiophenoimine)-co-poly(ethylenedioxy thiophene) star copolymer

A generation 1 poly(propylene thiophenoimine)-co-poly(ethylenedioxy thiophene) (G1PPT-co-PEDOT) star copolymer, which exhibits a strong optical absorption over a broad range in the ultraviolet–visible (UV-Vis) region and with good electro/conductive properties, was chemically prepared for the first time. Synthesis of the star copolymer, G1PPT-co-PEDOT was confirmed by spectroscopic studies. Indeed, the disappearance of the very high intensity bands, C–H bending at α-position (687 cm−1), and C=N stretching (1620 cm−1) in the Fourier transform infrared spectroscopy (FTIR) of G1PPT-co-PEDOT, which were initially present in the spectrum of the thiolated starting material, G1PPT, confirmed copolymerization. Furthermore, a large bathochromic shift in the onset wavelength of the UV-Vis absorbance spectra from 367 nm in G1PPT to 674 nm in G1PPT-co-PEDOT further attests of successful copolymerization. The electrochemical analysis of G1PPT-co-PEDOT achieved a highest occupied molecular orbital (HOMO) energy level value of 5.3 eV, which is reminiscent of the value for an ideal electron-donor material. Photoluminescence quenching of up to 82% was observed in solution blends of the G1PPT-co-PEDOT star copolymer and N,N′-diisopropyl naphthalene diimide (NDI)

Palladium-Gold Nanoalloy Surface Modified LiMn2O4 Cathode for Enhanced Li-Ion Battery

Au with Pd nanoparticles were synthesized and coated onto the spinel LiMn2O4 via a coprecipitation calcination method with the objective to improve the microstructure, conductivity, and electrochemical activities of pristine LiMn2O4. The novel LiPdAuxMn2-xO4 composite cathode had high phase purity, well crystallized particles, and more regular morphological structures with narrow size distributions. At enlarged cycling potential ranges the LiPdAuxMn2-xO4 sample delivered 90 mAh g−1 discharge capacity compared to LiMn2O4 (45 mAh g−1). It was concluded that even a small amount of the Pd and Au enhanced both the lithium diffusivity and electrochemical conductivity of the host sample due to the beneficial properties of their synergy

Comparative study of microwave assisted and conventional synthesis of novel 2-quinoxalinone3- hydrazone derivatives and its spectroscopic properties

A series of novel quinoxalin-2(1H)-one-3-hydrazone derivatives, 2a -8d were synthesized via condensation of 3-hydrazinoquinoxalin-2(1H)-one, 1, with the corresponding ketones under microwave irradiation. The microwave assisted reaction was remarkably successful and gave hydrazones in higher yield at less reaction time compared to conventional heating method. The chemical structures of the compounds prepared were confirmed by analytical and spectral data

Graphene Oxide Decorated Nanometal-Poly(Anilino-Dodecylbenzene Sulfonic Acid) for Application in High Performance Supercapacitors

Graphene oxide (GO) decorated with silver (Ag), copper (Cu) or platinum (Pt) nanoparticles that are anchored on dodecylbenzene sulfonic acid (DBSA)-doped polyaniline (PANI) were prepared by a simple one-step method and applied as novel materials for high performance supercapacitors. High-resolution transmission electron microscopy (HRTEM) and high-resolution scanning electron microscopy (HRSEM) analyses revealed that a metal-decorated polymer matrix is embedded within the GO sheet. This caused the M/DBSA⁻PANI (M = Ag, Cu or Pt) particles to adsorb on the surface of the GO sheets, appearing as aggregated dark regions in the HRSEM images. The Fourier transform infrared (FTIR) spectroscopy studies revealed that GO was successfully produced and decorated with Ag, Cu or Pt nanoparticles anchored on DBSA⁻PANI. This was confirmed by the appearance of the GO signature epoxy C⁻O vibration band at 1040 cm−1 (which decreased upon the introduction of metal nanoparticle) and the PANI characteristic N⁻H stretching vibration band at 3144 cm−1 present only in the GO/M/DBSA⁻PANI systems. The composites were tested for their suitability as supercapacitor materials; and specific capacitance values of 206.4, 192.8 and 227.2 F·g−1 were determined for GO/Ag/DBSA⁻PANI, GO/Cu/DBSA⁻PANI and GO/Pt/DBSA⁻PANI, respectively. The GO/Pt/DBSA⁻PANI electrode exhibited the best specific capacitance value of the three electrodes and also had twice the specific capacitance value reported for Graphene/MnO2//ACN (113.5 F·g−1). This makes GO/Pt/DBSA⁻PANI a very promising organic supercapacitor material