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Solar energy-powered adsorption-based atmospheric water harvesting (ABAWH) is an emerging technology for freshwater production, especially in water-scarce regions that are remote and landlocked. Numerous water adsorbents have been used in ABAWH devices to convert molecule to liquid water. However, it is still challenging to harvest water from the air in cold winter, owing to the water adsorption of sorbents decreasing significantly at low temperature. Herein, we designed and fabricated an ABAWH device by integrating composited ionic liquids (CILs) with carbon nanotubes (CNTs) photothermal materials on the surface of cotton rod fibers. CILs extract water from the air. CNTs enable light-to-heat conversion and drive the solar evaporation process. Importantly, the cotton rods offer a backbone porous structure to maintain its internal temperature at 20 °C under solar irradiation, and thus promote the water adsorption performance of CILs at low environmental temperature. Freshwater is successfully harvested under environment temperature of 6 °C, 30% RH and solar irradiation intensity of 0.6 kW m−2. The water yield can achieve 1.49 kg per m2 per day in an outdoor environment. We believe that the ABAWH device offers a promising approach to effectively harvest water from the air at low temperature and humidity conditions.

Planar-type perovskite solar cells (p-PSCs) based on SnO2 have garnered further attention due to their simple and low-temperature fabrication. Improving the critical properties of the electron transport layer (ETL) is an effective way to enhance the performance of p-PSC devices. Here, a brand-new method is developed to relieve the contact recombination caused by the rough fluorine-doped tin oxide (FTO) surface and further boosts the electrical concentration of the ETL. A SnO2-ethylene diamine tetraacetic acid (EDTA) acylamide compound (SEAC) with hydrogen bond-induced adjustable cluster size is reported for the first time. The rational choice of the SEAC cluster size is the key for obtaining the smooth interfacial morphology of the ETL on the rugged FTO substrate. In addition, the energy band gap decreases with the increasing cluster size, and consequently, results in improved electrical conductivity of the SEAC. The upshifted Fermi energy level leads to higher electron concentration, which is an important physical quantity of the ETL. The PSC devices based on the optimized SEAC achieve an improved power conversion efficiency of 21.29% with negligible J-V hysteresis due to significantly enhanced electron transport and reduced contact charge recombination at the ETL/perovskite interface. In general, this paper comes up with a unique strategy to improve the quality of the SnO2-based ETL.

Li metal is considered a highly desirable anode for next-generation high-energy-density rechargeable lithium batteries. However, irregular Li dendrite formation and infinite relative volume changes prevent the commercial adoption of Li-metal anodes. Here, electrophoretic deposition of black phosphorus (BP) on commercial Cu foam (BP@Cu foam) is reported to regulate Li nucleation for the first time. First-principles calculations reveal that the unique two-dimensional (2D) structure of BP is beneficial to Li intercalation and propagation. Compared with the random Li nucleation and growth on bare Cu foam, Li ions are preferably confined into the BP layers, which induces uniform Li nucleation at the early stage of the Li deposition and guides the following lateral Li growth on BP@Cu foam. In addition, the three-dimensional (3D) porous and conductive framework of Cu foams further mitigate the volume change and dissipate the current density. Attributing to these merits, the BP@Cu foam exhibits significantly enhanced Coulombic efficiency and cycling stability compared with bare Cu foam. In the full-cell configuration paired with a Li4Ti5O12 or LiFePO4 cathode, the BP@Cu foam also boosts the battery performances. This work provides new insights into the development of BP and other elaborate 2D materials for achieving dendrite-free Li-metal anodes.

Controllable three-dimensional villose titanium dioxide architectures grown on carbon textiles are fabricated by a facile one-step in-situ hydrothermal method at low temperatures. It has in fact been proven to be an effective method to reduce self-aggregation and promote lithium-ion intercalate/extract via building 3D architectures based on 2D conductive materials. More importantly, the freestanding electrodes without any addition of conductive agents and polymeric binders reveal significant improvement in high-rate capacity and cycling performance.

Herein, we demonstrate a sustainable strategy for scalable production of α-Fe2O3 nanocrystals on flexible carbon textiles via controllable chemical bath deposition process. The assembly of α-Fe2O3 nanocrystals is densely anchored onto the carbon textiles, and the temperature-dependent mass loading and crystal size of α-Fe2O3 are systematically investigated. As an integrated electrode for lithium-ion batteries, the optimized Fe2O3@CTs with ultrathin three-dimensional interconnected porous architectures achieves significantly enhanced cycling performance and rate capability attributing to the improved stability, electronic interconnection, and shortened solid state diffusion pathway for Li+ ions/electrons. After the reactivation of the precursor, the Li-ion batteries based on the recycled Fe2O3@CTs exhibits electrochemical performance with no decay compared to that of the devices based on the fresh products. This sustainable methodology, considering material abundance, eco-efficiency, synthetic approach and scalability, is of crucial importance to both academy and industry for achieving high-performance lithium-ion batteries.

We have demonstrate a facile strategy to achieve the controllable morphology transformation of TiO2 induced by the introduction of multi-walled carbon nanotubes. The intervention of functionalized carbon nanotubes (CNTs) is key to the formation of TiO2 nanopompons. Furthermore, the size of the obtained TiO2 nanopompons can be controlled by modulating the CNT amounts. The obtained TiO2 nanopompon-embedded CNT hybrid networks (TNP@CNT HNs) incorporate the advantages of hierarchical nanostructures and 3D interconnected conductive networks, including high surface area, uniform particle/pore size, short Li+ ion/electron transport pathway, and high electronic conductivity. These TNP@CNT HN-based anodes achieve a significant improvement in the insertion/extraction of Li+ ions and electrochemical performances via optimizing the CNT amounts and the size of the TiO2 nanopompons. The lithium-ion batteries based on the optimized TNP@CNT HNs exhibit excellent cycling stability (keeping approximately 200 mA h g−1 after 500 cycles at 2C rate, 1C = 170 mA g−1) and rate performance (approximately 125 mA h g−1 at 20C rate with a capacity retention of 77% after 2000 cycles).

Well-organized epsilon-MnO2 hollow spheres/reduced graphene oxide (MnO2HS/RGO) composites have been successfully constructed via a facile and one-pot synthetic route. The ε-MnO2 hollow spheres with the diameter of ∼500 nm were grown in situ with homogeneous distribution on both sides of graphene oxide (GO) sheets in aqueous suspensions. The formation mechanism of the MnO2HS/RGO composites has been systematically investigated, and a high specific capacitance and good cycling capability were achieved on using the composites as supercapacitors. The galvanostatic charge/discharge curves show a specific capacitance of 471.5 F g(-1) at 0.8 A g(-1). The hollow structures of ε-MnO2 and the crumpled RGO sheets can enhance the electroactive surface area and improve the electrical conductivity, thus further facilitating the charge transport. The MnO2HS/RGO composite exhibits a high capacitance of 272 F g(-1) at 3 A g(-1) (92% retention) even after 1000 cycles. The prominent electrochemical performance might be attributed to the combination of the pseudo-capacitance of the MnO2 nanospheres with a hollow structure and to the good electrical conductivity of the RGO sheets. This work explores a new concept in designing metal oxides/RGO composites as electrode materials.

We report a simple approach based on a chemical reduction method to synthesize aqueous inorganic ink com- prised of hexagonal MnO2 nanosheets. The MnO2 ink exhibits long-term stability and continuous thin films can be formed on various substrates without using any binder. To obtain a flexible electrode for capacitive energy storage, the MnO2 ink was printed onto commercially available A4 paper pretreated with multiwalled carbon nanotubes. The electrode exhibited a max- imum specific capacitance of 1035 F g � 1 (91.7 mF cm � 2 ). Paper- based symmetric and asymmetric capacitors were assembled, which gave a maximum specific energy density of 25.3 Wh kg � 1 and a power density of 81 kW kg � 1 . The device could maintain a 98.9 % capacitance retention over 10 000 cycles at 4 A g � 1 . The MnO2 ink could be a versatile candidate for large-scale production of flexible and printable electronic devices for energy storage and conversion.

Three-dimensional branched TiO2 architectures (3D BTA) with controllable morphologies were synthesized via a facile template-free one-pot solvothermal route. The volume ratio of deionized water (DI water) and diethylene glycol in solvothermal process is key to the formation of 3D BTA assembled by nanowire-coated TiO2 dendrites, which combines the advantages of 3D hierarchical structure and 1D nanoscale building blocks. Benefiting from such unique structural features, the BTA in full bloom achieved significantly increased specific surface areas and shortened Li(+) ion/electrons diffusion pathway. The lithium-ion batteries based on BTA in full bloom exhibited remarkably enhanced reversible specific capacity and rate performance, attributing to the high contact area with the electrolyte and the short solid state diffusion pathway for Li(+) ion/electrons promoting lithium insertion and extraction.

Manganese dioxides octahedral molecular sieve nanowires with 2 × 2 tunnels (designated OMS-2) and amorphous manganese dioxides were synthesized via a hydrothermal treatment and a sol–gel method, respectively. Amorphous MnO 2 nanoparticles were incorporated into the matrix of OMS-2 nanowires to form homogenous nanocomposites. The structures and morphologies of as-synthesized OMS-2 nanowires and amorphous MnO 2 nanoparticles were characterized using X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM). Electrochemical behaviors of the as-prepared nanocomposites with varying ratios were investigated by cyclic voltammetry (CV), galvanostatic charge/discharge and potentiostatic electrochemical impedance spectroscopy (EIS) using a three-electrode system in a 0.5 M Na 2 SO 4 aqueous solution. Pure OMS nanowires exhibit a specific capacitance of about 37 F g −1 , and amorphous MnO 2 nanoparticles demonstrate relatively higher specific capacitance of about 106 F g −1 at a scan rate of 2 mV s −1 . The enhancement of specific capacitance can be carried out by mixing OMS-2 nanowires and amorphous MnO 2 nanoparticles to form nanocomposites and the optimized mole ratio of OMS-2 nanowires to amorphous MnO 2 as 1:5 can be achieved. The improved specific capacitance can be attributed to the increase of electrode conductivity and the effective interfaces between MnO 2 active materials and electrolyte.

Submicrometer-sized monodispersed TiO2 spheres were synthesized by a controlled hydrolysis of titanium tetraisopropoxide (TTIP) and subsequent solvothermal treatment. The X-ray diffraction (XRD), scanning electron microscopy (SEM), and UV–visible spectroscopy analyses revealed that aqueous ammonia concentration and calcining temperature significantly influence the morphology, crystallization, dye loading, and light scattering capacity of TiO2 microspheres. And it was found that the TiO2 microspheres prepared by this method showed a good thermal stability of phase. Bilayered dye-sensitized solar cells (DSSCs) composed of TiO2 microspheres as the scattering cover layers and TiO2 nanocrystallines as the underlayer exhibited a remarkable improvement in the power conversion efficiency (8.25%) compared with the nanocrystalline TiO2 DSSC (6.38%), owing to high light scattering efficiency and the dye-loading capacity of the microsphere cover layer. In addition, electrochemical impedance spectra (EIS) and open-cir...

Three-dimensional LiNi 0.5 Mn 0.5 O 2 (3D-LiNi 0.5 Mn 0.5 O 2 ) nanostructures are in situ prepared using cryptomelane-type octahedral molecular sieve manganese dioxide (OMS-2) in the form of dendritic nanostructures as templates. The complete conversion of the OMS-2 precursor to layered α-NaFeO 2 -type LiNi 0.5 Mn 0.5 O 2 and the retention of the 3D dendritic nanostructures have been confirmed by XRD, FE-SEM, TEM, and HR-TEM. The as-synthesized nanostructured positive electrode exhibits a significant improvement in rate performance and cycling reversibility due to its unique nanostructures composed of single-crystalline LiNi 0.5 Mn 0.5 O 2 nanorods. And the influence of the assembly mode of nanosize LiNi 0.5 Mn 0.5 O 2 positive electrode material to its electrochemical performances has been investigated. The battery based on 3D-LiNi 0.5 Mn 0.5 O 2 retains a discharge capacity of 151.6 mAh g −1 (93% of the first discharge capacity) after 50 cycles. A specific discharge capacity of 141.8 mAh g −1 was retained at a rate of 3.2 C, which is about 80% of the capacity at a rate of 0.2 C.

The interaction between ZnO compact layer and TiCl 4 post-treatment on TiO 2 photoelectrode for dye sensitized solar cell (DSSC) is investigated. Photoelectrode combined the two modifications is designated as ZnO + 2l + TiCl 4 . It is found that after the TiCl 4 treatment the ZnO compact layer transforms to a bi-functional layer, which suppresses back electrons transfer from FTO to electrolyte and reduces the FTO/TiO 2 interfacial resistance. In addition, the newly formed TiO 2 coating generated by TiCl 4 post-treatment contains abundant and well dispersed Zn element, which further facilitates electron transfer at TiO 2 layer. Meanwhile, the electron lifetime in ZnO + 2l + TiCl 4 is the longest. Consequently, the overall energy conversion efficiency of the cell with ZnO + 2l + TiCl 4 is significantly enhanced to 8.9%, which is 8.8% higher than that with pure TiCl 4 post-treatment and 17.7% higher than that without any treatment. These results are verified by material characterization and corresponding opto-electrical properties measurements. Experimental results demonstrate this facile method is a more promising alternative to the conventional interface and surface modification in high efficient DSSCs.

A series of dye-sensitized solar cells (DSSCs) with different graphene-P25 (G-P25) photoelectrodes were prepared by a ball milling method. The influences of graphene on the structures and performance of G-P25 cells were studied. Studies indicated that the rutile contents in G-P25 photoelectrodes increased with increasing graphene-oxide (GO) additions and reached the maximum value at GO addition of 4.5 ml. And with the increase of GO additions, the porosity of the G-P25 photoelectrodes, the interface recombination resistances, and the short current densities increased. When the GO addition was 4.5 ml, the G-P25 cells showed the best performance with the largest interface recombination resistance of 15.12 Ω and the largest photoelectric conversion efficiency of 5.09%, which was remarkably higher than those of pure P25 DSSC. Since the tendency of the photoelectric conversion efficiency varying with the GO additions was in consistence with that of the rutile contents, the enhancement of the photoelectric conversion properties of the G-P25 DSSCs was preliminary attributed to the increase of the rutile contents and the porosity in the photoelectrodes due to graphene adding.

This paper reports an inverted fabrication process for the photoanode of a flexible dye sensitized solar cell (DSSC). This procedure involves assembling a free-standing TiO2 nanowires/nanoparticles hybrid membrane, via high temperature annealing, sputtering an indium tin oxide (ITO) layer onto this membrane, and transferring these onto a polydimethylsiloxane (PDMS) substrate. The inverted procedure prevents thermal decomposition of polymer substrate, whilst enabling effective thermal treatment of the functionalized titanium oxide. The flexible DSSC fabricated in this way has an efficiency of 2.7%, which is comparable with rigid device constructed using similar materials.

A convenient way is experimented to reduce the amount of dye in quasi-solid DSSCs but raise open-circuit photovoltage and photocurrent density. AFM stereoscopic morphology and calculated roughness of root mean square indicates looser porous configuration is formed in the modified TiO 2 film which is beneficial for the penetration of quasi-solid electrolyte. Decreased content of sensitized dye is confirmed by UV–vis absorption spectra. Electrochemical impedance spectroscopy is employed to characterize the transport and recombination of electrons and also to assess the penetration of quasi-solid electrolyte in the porous matrix of DSSCs. Analysis of charge-transfer resistance and dc resistance of impedance of diffusion of tri-iodide reveals enhanced mobility of tri-iodide in DSSCs. Photovoltaic parameters of quasi-solid DSSCs show an increased open-circuit photovoltage due to the enlarged photoelectrode film porosity and the shift of redox level. Better penetration of quasi-solid electrolyte has a predominant advantage over the negative effect caused by lose of photocurrent, to some extent, as a result of decreased adsorbed dye. The best result of this beneficial outcome occurs when the PEG loading is 20%, giving an overall cell efficiency of 5.1%.

The electrochemical and tribocorrosion behaviors of Ti–6Al–4V, 316 stainless steel and Monel K500 alloys sliding against Al 2 O 3 in artificial seawater are investigated in this paper. It can be observed that the open circuit potential drops down to more negative values due to the removal of passive film. And a rapid dissolution occurs in the wear track compared with the unworn area. The wear loss polarized in cathodic potential is lower than that in anodic potential and open circuit potential conditions, because the material deterioration is enhanced by corrosive attack. The wear volumes of 316 stainless steel are much higher than the ones measured for Ti–6Al–4V and Monel K500 alloys. Friction coefficients are significant large in cathodic polarization compared with anodic polarization for all alloys. Moreover, the 316 stainless steel exhibits large friction coefficients compared with Ti–6Al–4V and Monel K500 alloys.

Highly uniform and transparent polyaniline (PANI) electrodes that can be used as counter electrodes in dye-sensitized solar cells (DSSCs) were prepared by a facile in situ polymerization method. They were used to fabricate a novel bifacially active transparent DSSC, which showed conversion efficiencies of 6.54 and 4.26% corresponding to front- and rear-side illumination, respectively. Meanwhile, the efficiency of the same photoanode employing a Pt counter electrode was 6.69%. Compared to conventional Pt-based DSSCs, the design of the bifacial DSSC fabricated in this work would help to bring down the cost of energy production due to the lower cost of the materials and the higher power-generating efficiency of such devices for their capabilities of utilizing the light from both sides. These promising results highlight the potential application of PANI in cost-effective, transparent DSSCs.

A novel and thin ZnO compact blocking film is employed at the interface of fluorine-doped tin oxide (FTO) substrate and mesoporous TiO2, and its influence on dye-sensitized solar cells (DSSCs) is investigated. The ZnO film prepared by spin-coating method on FTO is characterized by energy-dispersive X-ray spectroscopy (EDX), scanning electron microscopy (SEM), and UV–vis spectrophotometer. The ZnO film is firstly employed as an energy barrier between FTO and mesoporous TiO2 film in DSSCs, which improves open-circuit photovoltage (Voc) and fill factor (FF) with compensation of Jsc decrease, finally increasing energy conversion efficiency from 5.85% to 6.70%. Electrochemical impedance spectra (EIS) analysis and open-circuit voltage decay (OCVD) technique reveal that the existence of the energy barrier not only resulted in the effect of suppressing back electrons transfer from FTO to electrolyte but also blocking the electrons injection from the conductive band of TiO2 to FTO. The former effect effectively reduces the recombination which occurs in the region of FTO substrate, and the latter leads to remarkable increment of electron density in the TiO2, thus resulting in enhanced Voc and FF. These results suggest that the methodology of introducing the semiconductor with a more negative conduction band edge than TiO2 as the compact blocking film in DSSCs may be feasible.

A PEO/P(VDF-HFP) composite polymer electrolyte was modified by different amounts of NH 2 -end functional silane (3-amonopropyltriethoxysilane, APTS). Fourier transform infrared (FT-IR), X-ray diffraction (XRD) and differential scanning calorimetry (DSC) were carried out to examine the configuration changes of the polymer electrolyte. The newly formed Si–O–Si network and interactions influenced the ionic conductivity of the APTS-modified polymer electrolyte and also enhanced the connection of the polymer electrolyte with the electrodes of the dye sensitized solar cells (DSSCs). The cyclic voltammograms and electrochemical impedance measurements indicated that the APTS deprotonated the TiO 2 photoanode surface and negatively changed the Fermi energy level and the conduction band edge to the vacuum level. This effectively reduced the interface recombination in the DSSC and improved the open circuit voltage. With moderate APTS content (0.1 M) modification, the DSSC exhibited a 58 mV improvement of photovoltage and an improved performance of 5.08% compared with 3.74% of the original DSSC.

This paper deals with the distribution of generated microcrystallites in borate glass irradiated by 120 fs laser pulses at a central wavelength of 800 nm. Raman spectroscopy is used to investigate the distribution of the high and low temperature phases of barium metaborate crystals generated in the borate glass. In combination with a microexplosion model, bond-breaking induced by laser irradiation is served as the origin of the formation of BBO crystals. Depending on the laser fluence and cooling conditions, the distribution mechanisms have been discussed.

Novel architectured LiFePO4 (LFP) that consisted of ordered LFP nanocubes was prepared through a facile hydrothermal method using polyethylene glycol (PEG) as a surfactant. The micro/nanostructured LFP with various morphologies ranging from cube cluster to rugby-like structure was synthesized via controlling the pH values of the precursor. A reasonable assembly process elucidating the formation of the hierarchical structure is also provided based on the experimental results. After a combination of carbon (C) coating and reduced graphene oxide (RGO) wrapping, the obtained LFP/C/RGO composites exhibit enhanced electrochemical performance compared to that of blank LFP synthesized under the same condition. Among as-synthesized cube-cluster-like, dumbbell-like, rod-like, and rugby-like composites, the rugby-like LFP/C/RGO reveal the best electrochemical properties with the discharge specific capacity of ∼150 mA h g(-1) after 100 cycles and a high reversible specific capacity of 152 mA h g(-1) at 0.1 C. The prepared LFP/C/RGO composite can be a promising cathode material for high energy, low cost, and environmentally friendly lithium-ion batteries.

A CTCs detection assay using transparent MnO2 nanospheres thin films to capture and release of CTCs is reported. The enhanced local topography interaction between extracellular matrix scaffolds and the antibody-coated substrate leads to improved capture efficiency. CTCs captured from artificial blood sample can be cultured and released, represent a new functional material capable of CTCs isolation and culture for subsequent studies.

The applications of lanthanide-doped upconversion nanocrystals in biological imaging, photonics, photovoltaics and therapeutics have fuelled a growing demand for rational control over the emission profiles of the nanocrystals. A common strategy for tuning upconversion luminescence is to control the doping concentration of lanthanide ions. However, the phenomenon of concentration quenching of the excited state at high doping levels poses a significant constraint. Thus, the lanthanide ions have to be stringently kept at relatively low concentrations to minimize luminescence quenching. Here we describe a new class of upconversion nanocrystals adopting an orthorhombic crystallographic structure in which the lanthanide ions are distributed in arrays of tetrad clusters. Importantly, this unique arrangement enables the preservation of excitation energy within the sublattice domain and effectively minimizes the migration of excitation energy to defects, even in stoichiometric compounds with a high Yb(3+) content (calculated as 98 mol%). This allows us to generate an unusual four-photon-promoted violet upconversion emission from Er(3+) with an intensity that is more than eight times higher than previously reported. Our results highlight that the approach to enhancing upconversion through energy clustering at the sublattice level may provide new opportunities for light-triggered biological reactions and photodynamic therapy.

The end-functional silicone coupling agent (dodecyl-trimethoxysilane, DTMS for short) was used to modify the PEO/P(VDF-HFP)/SiO(2) nanocomposite polymer electrolyte (CPE) and the different amounts of DTMS modification effects were studied. The experiments showed the silicone coupling agent with hydrophobic alkyl chains (-C(12)H(25)) chemically engineered on the SiO(2) nanoparticles, and formed a Si-O-Si cross-linked network in the new nanocomposite polymer electrolyte. Proper content of DTMS modified CPE exhibited improved ionic conductivity and the connection with the photoanode and counter electrode. However, much higher content of the DTMS modification changed the conformation of the polymer network and reduced the ionic movement. Compared with the performance (3.84%) of the original DSSC, the DSSC with functional silicone coupling agent modified CPE (DTMS:SiO(2) = 2:1, mol ratio) exhibited improved J(sc) (7.94 mA cm(-2)), V(oc) (0.624 V) and optimal efficiency (5.2%) (measured at AM1.5, light intensity of 58.4 mW cm(-2)). The V(oc) of the silicone coupling agent modified polymer electrolyte DSSC is obviously improved, which is mainly due to that the hydrophobic alkyl chain end groups formed an insulating layer that retarded the electron recombination at the TiO(2) nanoporous photoanode/polymer electrolyte interface. The DTMS:SiO(2) = 2:1 modified CPE type DSSC exhibited a performance of 6.42% at a light intensity of 32.1 mW cm(-2) and 4.94% at 99.2 mW cm(-2).

A quasi-solid-state dye-sensitized solar cell employing a poly(ethylene oxide)-poly(vinylidene fluoride) (PEO-PVDF)/TiO2 gel electrolyte modified by various concentrations of water and ethanol is described. It is shown that the introduction of water and ethanol prevents the crystallization of the polymer matrix, and enhances the free I(-)/I(3)(-) concentration and the networks for ion transportation in the electrolyte, thus leading to an improvement in conductivity. A high energy conversion efficiency of about 5.8% is achieved by controlling the additive concentration in the electrolyte. Optimization of the additive-modified electrolyte performance has been obtained by studying the cross-linking behavior of water and ethanol with Fourier transform infrared (FTIR), differential scanning calorimetry (DSC) and viscosity measurements, and the electrical conduction behavior of the electrolyte with impedance spectra measurements.

A fibrous polyaniline (PANI) thin film has been fabricated from prepared PANI nanofiber solution by Marangoni flow. The PANI retained its original fiber morphology after being deposited into films and formed highly interconnected network structures, which leads to an excellent electrochemical catalytic activity. This PANI thin film was applied in dye sensitized solar cell (DSSC) as counter electrode. A power conversion efficiency (PCE) of 3.8% of the DSSC by this PANI counter electrode was obtained without optimization of synthesis conditions, compared with 5.1% PCE by traditional Pt counter electrode. Better performances are attainable by improving the conductivity of PANI with acid doping process to decrease the sheet resistance of this electrode. Facile synthesis process and good performance of these nanofibrous PANI thin films highlight the potential large scale applications for low-cost counter electrode in DSSCs.

This paper reports experimental studies using the photoelectrocatalytic effect to eliminate a fundamental limit of photocatalysis - the recombination of photo-excited electrons and holes. The fabricated reactor has a planar reaction chamber (10 × 10 × 0.1 mm(3)), formed by a blank indium tin oxide glass slide, an epoxy spacer and a BiVO(4)-coated indium tin oxide glass substrate. A blue light-emitting diode panel (emission area 10 × 10 mm(2)) is mounted on the cover for uniform illumination of the reaction chamber. In the experiment, positive and negative bias potentials were applied across the reaction chamber to suppress the electron/hole recombination and to select either the hole-driven or electron-driven oxidation pathway. The negative bias always exhibits higher performance. It is observed that under -1.8 V the degradation rate is independent of the residence time, showing that the accompanying electrolysis can solve the oxygen deficiency problem. The synergistic effect of photocatalysis and electrocatalysis is observed to reach its maximum under the bias potential of ± 1.5 V. The photoelectrocatalytic microreactor shows high stability and may be scaled up for high-performance water purification.

Three-dimensional silver-embedded porous silicon (3D Ag@porous silicon) micronparticles were synthesized by a facile and low cost method via a metal-assisted chemical etching process for the first time. The electrode based on this 3D Ag@porous silicon anode material reveals a significant improvement in the electrochemical performance that results from its unique interconnected 3D network structure and the existence of high conductive silver nanoparticles encapsulated in the matrix of porous silicon. The battery based on 3D Ag@porous silicon micronparticles still retains a discharge capacity of 784 mA h g−1 after 50 cycles, which is more than two times larger compared with that of graphite (∼372 mA h g−1). These results suggest that this facile and low cost methodology for preparation of a porous silicon anode can be extended to industrial production.

LiNi0.5Mn0.5O2 nanoarchitectured spheres (NA-LiNi0.5Mn0.5O2) have been synthesized via an in situ conversion route derived from the use of γ-MnO2 hollow nanostructured spheres. The complete conversion of the γ-MnO2 precursor to layered α-NaFeO2-type NA-LiNi0.5Mn0.5O2 has been confirmed by XRD, FE-SEM, TEM, and HR-TEM. This NA-LiNi0.5Mn0.5O2 cathode exhibits a remarkable enhancement of rate performance compared with that of LiNi0.5Mn0.5O2 particles prepared by a conventional solid-state reaction method (SS-LiNi0.5Mn0.5O2). The batteries based on NA-LiNi0.5Mn0.5O2 retain a discharge capacity of 153.5 mA h g−1 (93% of the first discharge capacity) after 75 cycles. A specific discharge capacity of 121.9 mA h g−1 was retained at a rate of 3.2 C, which is about 70% of the capacity at a rate of 0.2 C.

To strengthen the adhesion of platinum layer to counterelectrodes of dye sensitized solar cells, titanium thin film has been utilized as adhesion layer between platinum and substrate [Wei et al., Appl. Phys. Lett. 90, 153122 (2007)]. In our study, platinum/titanium bilayer counterelectrodes were fabricated by magnetron sputtering. The structural, electrical, and electrochemical properties of the bilayer counterelectrode were studied by varying the thickness of both platinum and titanium layers. The influence of both electrochemical active surface and crystallite size on charge transfer resistance of the bilayer counterelectrode was explored. From these evaluations, it was found that the as-prepared titanium layer was almost amorphous, and intermetallic phase was formed between platinum and titanium layers. As expected, sheet resistance of the electrode decreased with the increase in deposition time of both platinum and titanium layers. Metal titanium was found to be inert in the catalyzing reduction in tr...