PEDOT electrodes for triboelectric generator devices

Triboelectric generators (TEGs) are devices that convert mechanical energy to electrical energy through triboelectric charging of different material surfaces at periodic contact. Typically, such devices consist of two dielectric contacting layers with electrodes attached on the non-contacting sides but alternatively, one material can simultaneously serve as both a contacting and an electrode material. In this work, we report the use of poly(3,4-ethylenedioxythiophene) (PEDOT) for TEG device were PEDOT film serves as both a contacting surface to PDMS and as an electrode. Two different PEDOT films were prepared on glass substrates by vapour-phase polymerization (VPP) and VPP combined with electropolymerization method and compared as TEG electrodes. Additionally, PEDOT/poly(1,6-hexanediol-co-citric acid) (PHC) composite films were prepared by using solution casting polymerization. These methods yielded PEDOT films with different morphology, surface roughness and conductivity. Best performance was demonstrated for the PEDOT film with the lowest surface roughness (1.88 nm RMS), prepared by VPP method, which generated peak current of 0.45 mA/m² and power density of 95 W/m², outperforming Sn doped In₂O₃ electrode approximately by threefold in the same experimental setup.     

Biohydrogen by Rhodobacter sphaeroides during photo-fermentation: Mixed vs. sole carbon sources enhance bacterial growth and H2 production

Mixed carbon sources fermentation by bacteria is a promising approach for biohydrogen (H₂) production biotechnology. In the present study, growth and Н₂ production by purple bacteria Rhodobacter sphaeroides MDC6521 during mixed carbon sources (succinate + acetate, succinate + malate, and malate + acetate) photo-fermentation was investigated. The growth rate of bacteria in mixed carbon sources containing medium was of ∼0.33 h⁻¹ which was considerably higher (1.3–1.7-fold) compared with sole carbon substrate containing one. Moreover, the H₂ production during photo-fermentation of succinate and acetate mixture was of ∼6.5 mmol H₂ g⁻¹ (dry weight of biomass) and significantly more (∼2–3-fold) than that with appropriate sole sources and higher (1.5-fold) than that with succinate and malate mixture. Probably, supplementation of the mixed carbon sources into bacterial culture alters the mode of metabolism, resulting in enhanced H₂ production, thus they can be preferable compared to the sole carbon source. The changed F_OF₁-ATPase activity of membrane vesicles suggested its important role in the increase of Н₂ production efficiency. The results showed that mixed carbon sources provide more H₂ than the sole carbon substrates and succinate with acetate mixture is better than succinate with malate.     

Facile fabrication of a binary NiCo phosphide with hierarchical architecture for efficient hydrogen evolution reactions

Exploring and designing efficient non-noble catalysts formed by element doping and nanostructure modification for the hydrogen evolution reaction (HER) is of critical importance with respect to sustainable resources. Herein, we have prepared a three-dimensional binary NiCo phosphide with hierarchical architecture (HA) composed of NiCoP nanosheets and nanowires grown on carbon cloth (CC) via a facile hydrothermal method followed by oxidation and phosphorization. Due to its unique hierarchical nanostructure, the NiCoP HA/CC electrocatalyst exhibits excellent performance and good working stability for the HER in both acidic and alkaline conditions. The obtained NiCoP HA/CC shows excellent HER activity with a low potential of 74 and 89 mV at 10 mA cm⁻², a small Tafel slope of 77.2 and 99.8 mV dec⁻¹ and long-term stability up to 24 h in acidic and alkaline electrolyte, respectively. NiCoP HA/CC, a non-noble metal material, is a promising electrocatalyst to replace noble metal-based electrocatalysts for the HER.     

Graphitized carbon nanocages/palladium nanoparticles: Sustainable preparation and electrocatalytic performances towards ethanol oxidation reaction

Graphitized carbon (GC) nanocages have been successfully prepared via a sustainable carbon powder buried-type Ni catalysis-growth technology from Tween-80 molecule precursor. The GC nanocages are used as support for the further construction of GC/Pd electrocatalyst towards ethanol oxidation reaction. The material structures and surface morphologies are studied by XRD, SEM and TEM techniques. The electrochemical properties are investigated by CV, LSV, EIS and CP techniques. The results showed that GC nanocages have good graphited structure and plentiful opening gaps, and the Pd nanoparticles were evenly distributed on the inner and outer surfaces of GC nanocages. The GC/Pd electrocatalyst exhibits excellent electrocatalytic performance towards ethanol oxidation. The positive scanning peak current density of GC/Pd electrode is up to 1612 A/g Pd in 1.0 mol/L NaOH +1.0 mol/L ethanol electrolyte, which is much higher than those (500–1100 A/g Pd) of traditional Pd electrodes supported with carbon nanotubes or graphene nanosheets.     

Synergistic effects of advanced oxidization reactions in a combination of TiO2 photocatalysis for hydrogen production and wastewater treatment applications

In this paper, the synergistic effects of advanced oxidization reactions in a combination of TiO₂ photocatalysis are comparatively investigated for hydrogen production and wastewater treatment applications. An experimental study is conducted with a photoelectrochemical reactor under a UV-light source. TiO₂ is selected as the photocatalyst due to the high corrosion resistant nature and ability to form hydroxyl radicals with the interaction with photons. The synergetic effects of advanced oxidization processes (AOPs) such as Fenton, Fenton-like, photocatalysis (TiO₂/UV) and UV photolysis (H₂O₂/UV) are investigated individually and in a combination of each other. The Fenton type reagent in the reactor is formed by anodic sacrificial of stainless-steel electrode with the presence of H₂O₂. The influences of various parameters, including pH level, type of the electrode and electrolyte and the UV light, on the performance of the combined system are also investigated experimentally. The highest chemical oxygen demand (COD) removal efficiency is observed as 97.9% for the experimental condition which combines UV/TiO₂, UV/H₂O₂ and photo-electro Fenton type processes. The maximum hydrogen production rate from the photoelectrolysis of wastewater is obtained as 7.0 mg/Wh for the experimental condition which has the highest rate of photo-electro Fenton type processes. The average enhancement with the presence of UV light on hydrogen production rates and COD removal efficiencies are further calculated to be 3% and 20%, respectively.     

SQM-OTFT: A compact model of organic thin-film transistors based on the symmetric quadrature of the accumulation charge considering both deep and tail states

A physically-based compact model of organic thin-film transistors suitable for CAD simulators is proposed. It is worked out by means of a newly developed and particularly simple form of the charge-sheet model: the symmetric quadrature of the accumulation charge. The model is based on the variable-range hopping and accounts for both deep and tail states. It is simple, symmetric, accurately accounts for the below-threshold, linear, and saturation regimes via a unique formulation. The symmetric quadrature is accurate within 5% in all regions of operation and the resulting current model is suitable both for p- and n-type transistors. The model leads to a significant simplification of the drain current and of the quasi-static expressions of the terminal charges based on the Ward–Dutton partition. Finally, the symmetric quadrature leads to an explicit and analytically tractable solution for the surface potential as a function of position in the device channel that can be extremely useful to implement advanced physical effects.     

Nanostructured active chitosan-based films for food packaging applications: Effect of graphene stacks on mechanical properties

Bioactive food-preserving materials are based on the use of a natural antimicrobial compound loaded in a carrier material, which is able to trigger its release when requested and to modulate the rate of release, thus using either toxic or inhibitory properties against pathogens or bacteria due to food decomposition. In this study, the Schiff base formation for chitosan functionalization was achieved by the reaction of chitosan with cinnamaldehyde at different concentrations. Cinnamaldehyde is an aromatic α,β-unsaturated aldehyde, and the major component in essential oils from some cinnamon species. It has been shown to exert antimicrobial action against a large number of microorganisms including bacteria, yeasts, and mould. The formation of the Schiff base is reversible under suitable conditions, and this might allow the release of the active cinnamaldehyde from chitosan, used as the carrier. The reaction kinetics was investigated by means of rheological measurements, while infrared spectroscopy was used to assess the efficacy of the functionalization. The addition of nanometric graphene stacks to the cinnamaldehyde-functionalized chitosan films was evaluated with the aim to increase the mechanical properties of the film. Finally, the films were tested for antifungal properties with bread slices against a selected mould line.     

A low-cost and low-temperature processable zinc oxide-polyethylenimine (ZnO:PEI) nano-composite as cathode buffer layer for organic and perovskite solar cells

Nanocomposite buffer layer based on metal oxide and polymer is merging as a novel buffer layer for organic solar cells, which combines the high charge carrier mobility of metal oxide and good film formation properties of polymer. In this work, a nanocomposite of zinc oxide and a commercialized available polyethylenimine (PEI) was developed and used as the cathode buffer layer (CBL) for the inverted organic solar cells and p-i-n heterojunction perovskite solar cells. The cooperation of PEI in nano ZnO offers a good film forming ability of the composite material, which is an advantage in device fabrication. In addition, power conversion efficiency (PCE) of the ZnO:PEI CBL based device was also improved when compared to that of ZnO-only and PEI-only devices. The highest PCE of P3HT:PC₆₁BM and PTB7-Th:PC₆₁BM devices reached to 3.57% and 8.16%, respectively. More importantly, there is no obvious device performance loss with the increase of the layer thickness of ZnO:PEI CBL to 60 nm in organic solar cells, which is in contrast to the PEI based devices, whose device performance decreases dramatically when the PEI layer thickness is higher than 6 nm. Such a nano composite material is also applicable in inverted heterojunction perovskite solar cells. A PCE of 11.76% was achieved for the perovskite solar cell with a thick ZnO:PEI CBL (150 nm) CBL, which is around 1.71% higher than that of the reference cell without CBL, or with ZnO CBL. In addition, stability of the organic and perovskite solar cells having ZnO:PEI CBL was also found to be improved in comparison with that of PEI based device.     

Tuning color-correlated temperature and color rendering index of phosphorescent white polymer light-emitting diodes: Towards healthy solid-state lighting

We report on efficient solution-processed phosphorescent white polymer light-emitting diodes (WPLEDs) with tunable color-correlated temperature (CCT) and color rendering index (CRI), through rationally controlling the composition of the emission layer (EML) based on a near-infrared (NIR)-emitting dinuclear cyclometalated platinum (II) complex bridged with NˆS anionic ligand, named (niq)₂Pt₂(μ-C₈PhOXT)₂ (Pt-1, in which PhOXT is 5-(phenyl-1,3,4-oxadiazole)-2-thiol, niq is 1-naphthylisoquinolinato), a sky-blue emitter iridium (III) bis[(4,6-di-fluorophenyl)-pyridinato-N,C2] (picolinate) (FIrpic), and a yellow emitter bis[2-(thieno[3,2-c]pyridin-4-yl)phenyl]iridium(III)(acetylacetonato) (PO-01). One of the best three-color WPLEDs shows a CCT of 3246 K as well as an excellent high CRI of 87, which are greatly beneficial in reducing deep-blue light damage and simultaneously meet the requirement for good color reproduction. Meanwhile, the relevant WPLED also achieves a maximum current efficiency of 12.1 cd/A, corresponding to an external quantum efficiency of 10.6%. This work presents an effective approach through rational combination of sky-blue, yellow, and NIR emitters towards high-performance solution-processable WPLEDs with a physiologically-friendly CCT and a high CRI.     

Numerical investigation on the loading-delamination-unloading behavior of adhesive joints

An elastic-plastic interface model at finite deformations is utilized to investigate the irreversible delamination behavior of adhesive joints subjected to loading-delamination-unloading. The interface model accounts for the irreversible delamination in the fracture process zone induced by the localized plastic deformation and damage. The interfacial parameters in the cohesive model are obtained by fitting the available experimental data. Results suggest that the cohesive model can capture the irreversible delamination failure behavior observed in adhesively bonded joints during a loading-unloading cycle. The overall nonlinear response is dominated by the cohesive strength and initial damage displacement jump. Further, we also investigate the effect of the ductile mechanisms for the bulk layer on the competition between the plastic deformation of the bulk layer and the delamination of the interface. It is observed that the degradation of unloading stiffness is attributed to the inelastic behavior of the interface.