Preparation and performance of dye-sensitized solar cells based on ZnO-modified TiO_2 electrodes

The ZnO-modified TiO2 electrode was prepared by adding Zn（CH3COO）2·2H2O to the TiO2 colloid during the sol-gel production process, and was used in dye-sensitized solar cells （DSCs）. The open circuit voltage （Voc） and fill factor （if） of the cells were improved sig- nificantly. The performances of the ZnO-modified TiO2 electrode such as dark current, transient photocurrent, impedance, absorption spectra, and fiat band potential （Vfb） were investigated. It is found that the interface charge recombination impedance increases and Vfb shifts about 200 mV toward the cathodic potential. The effect mechanism of ZnO modification on the performance of DSCs may be that ZnO occupies the surface states of the TiO2 film.

Sensitization of Microporous Nanocrystalline TiO_2 Electrode with Quantum Sized RuS2 Particles

The microporous nanocry'sta1line TiO2 electrode with large surface roughness factor hasbeen prepared on a conducting glass support. Modification of the TiO2 electrode by in situ preparingquantum sized RuS2 particles on the surface of TiO2 electrode extends the optical absorptionspectrum and photocurrent action specmim into visible region. In addition, compared with RuS2 bulknlaterials- a blue shifi in both absorption spectrum and photocurrent action speCtrum of RuS2rriO2elcctrode is obserived and explained in terms of quantum sized effect.

Electrically enhanced photodegradation of an azodye(Acid Orange II) using a Pt/TiO_2 film electrode irradiating with an UV lamp

A photoelectrochemical process in the degradation of an azodye (Acid Orange II) on a Pt/TiO 2 film electrode was investigated. By using the glass device and the voltage stabilized source of direct current, decolorization ratios higher than 78% were observed during a period of 5h. Comparing this value with the sum of the decolorization ratios obtained by a sole application of electrochemical(lower than 3%) and photochemical(about 23%) procedures, a significant synergic effect between both processes was observed. The effects of adscititious voltage and pH value on the decolorization ratios were obvious while the effect of the amount of aeration was minor.

Composite Electrode SnO_2/TiO_2 for Dye-Sensitized Solar Cells

Composite nanoporous electrode SnO2/TiO2 was fabricated for the dye sensitized solar cell (DSSC) with N3 (Cis-Ru). After introducing of TiO2, the open-circuit photovoltage (Voc) was higher than that of the pure SnO2 electrode, while short-circuit photocurrent (Isc) was varied with the ratio of the TiO2. Appropriate content of the TiO2 can be beneficial to the efficiency of the solar cell, and it gives negative impact on the composite electrode when the content of TiO2 is higher.

Photoelectrochemical Character of TiO_2 Nanocrystalline Electrodes Sensitized by Aluminum Phthalocyanines Modified with Sulfonate Groups

Particular kinds of TiO2 nanocrystalline electrodes were sensitized by aluminum phthalocyanines modified with sulfonate groups [ Al（OH） PcSm ]. It was found that in the red region, the electrodes show obvious photoelectrical responses. The surface photovoltage spectra and photocurrent action spectra indicate that in the red region, the monomers of aluminum phthalocyanines have a greater influence on the determination of the photoelectrical response of TiO2 electrodes than the dimers. The dye-sensitized solar cells were obtained by using the aluminum phthalocyaninessensitized TiO2 electrodes and Pt electrodes, which have an open circuit photovoltage of 360 mV, a short circuit photocurrent of 39. 4 μA/cm^2 , a fill factor of 0. 54 and a maximum power output of 7.65 μW/cm^2 under a light intensity of 50 mW/cm^2.

A Dye-sensitized Nanocrystalline Solid State Photovoltaic Cell

A new type of dye-sensitized nanocrystalline solid state photovoltaic cell based on the wide band gap n-TiO2/p-CuI heterojunction was fabricated. Tetra-carboxyphenyl porphyrine (TPP-(COOH)(4)), squarylium cyanine derivative (SQ-(CH2),(SO3Py+)-Py-.) and ruthenium bipyridyl complex (RuL2(NCS)(2)) were used as photosensitizers. Larger photocurrents and photovoltages were shown in the cell sensitized by ruthenium bipyridyl complex and can be further increased by intercalation of a TiO2 thin underlayer.

An Effective Novel ReactionSystem For The Photo Degradation of Aqueous Organic Pollutants

A novel reaction system consisted of a supported TiO2 film electrode, a Ru?Ti oxide film electrode and air (oxygen) electrode is reported. The air (oxygen) electrode can provide H2O2 continuously for homogeneous photochemical oxidation reaction on the spot. In this reactor, degradation reaction of aniline occur from interface of TiO2 film to all solution which is irradiated by ultraviolet ray. The degradation rate of aniline was characterized by measuring the change of chemical oxygen demand (COD) in solution under different conditions. It was found that the degradation rate of aniline in the novel system increased apparently as compared with single heterogeneous photocatalysis and homogeneous photochemistry system. It can be explained in terms of combining acts of heterogeneous photocatalysis and homogeneous photochemistry.

Enhanced Visible-Light-Induced Photoelectrocatalytic Degradation of Methyl Orange by CdS Sensitized TiO2 Nanotube Arrays Electrode

In this work, CdS sensitized TiO2 nanotube arrays （CdS/TiO2NTs） electrode was synthesized with the CdS deposition on the highly ordered titanium dioxide nanotube arrays （TiO2NTs） by sequential chemical bath deposition method （S-CBD）. The as-prepared CdS/TiO2NTs was characterized by field-emission scanning electron mi- croscopy （FE-SEM） and X-ray diffraction （XRD）. The results indicated that the CdS nanoparticles were effectively deposited on the surface of TiOeNTs. The amperometric I-t curve on the CdS/TiO2NTs electrode was also presented. It was found that the photocurrent density was enhanced significantly from 0.5 to 1.85 mA/cm2 upon illumination with applied potential of 0.5 V at the central wavelength of 253.7 nm. The photoelectrocatalytic （PEC） activity of the CdS/TiO2NTs electrode was investigated by degradation of methyl orange （MO） in aqueous solution. Compared with TiO2NTs electrode, the degradation efficiencies of CdS/TiO2NTs electrode increased from 78% to 99.2% under UV light in 2 h, and from 14% to 99.2% under visible light in 3 h, which was caused by effective separation of the electrons and holes due to the effect of CdS, hence inhibiting the recombination of electron/hole pairs of TiO2NTs.

Engineering two-dimensional pores in freestanding TiO_2/graphene gel film for high performance lithium ion battery

As the key component of electrochemical energy storage devices, an electrode with superior ions transport pores is the important premise for high electrochemical performance. In this paper, we developed a unique solution process to prepare freestanding TiO_2/graphene hydrogel electrode with tunable density and porous structures. By incorporating room temperature ionic liquids（RTILs）, even upon drying, the non-volatile RTILs that remained in the gel film would preserve the efficient ion transport channels and prevent the electrode from closely stacking, to develop dense yet porous structures. As a result, the dense TiO_2/graphene gel film as an electrode for lithium ion battery displayed a good gravimetric electrochemical performance and more importantly a high volumetric performance.

Enhanced photoelectrocatalytic degradation of ammonia by in situ photoelectrogenerated active chlorine on TiO_2 nanotube electrodes

TiO2 nanotube （TINT） electrodes anodized in fluorinated organic solutions were successfully prepared on Ti sheets. Field-emission scanning electron microscopy （FE-SEM） and X-ray diffraction （XRD） were performed to characterize the TiNT electrodes. The linear voltammetry results under irradiation showed that the TiNT electrode annealed at 450℃ presented the highest photoelectrochemical activity. By combining photocatalytic with electrochemical process, a significantly synergetic effect on ammonia degradation was observed with Na2SO4 as supporting electrolyte at pH 10.7. Furthermore, the photoelectrocatalytic efficiency on the ammonia degradation was greatly enhanced in presence of chloride ions without the limitation ofpH. The degradation rate was improved by 14.8 times reaching 4.98 × 10^-2 min^-1 at pH 10.7 and a faster degradation rate of 6.34 × 10^-2 min^-1 was obtained at pH 3.01. The in situ photoelectrocatalytic generated active chlorine was proposed to be responsible for the improved efficiency. On the other hand, an enhanced degradation of ammonia using TiNT electrode fabricated in fluorinated organic solution was also confirmed compared to TiNT electrode anodized in fluorinated water solution and TiO2 film electrode fabricated by sol-gel method. Finally, the effect of chloride concentration was also discussed.

Pd-MnO_2 nanoparticles/TiO_2 nanotube arrays(NTAs) photo-electrodes photo-catalytic properties and their ability of degrading Rhodamine B under visible light

Pd-MnO2/TiO2 nanotube arrays（NTAs） photo-electrodes were successfully fabricated via anodization and electro deposition subsequently; the obtained Pd-MnO2/TiO2 NTAs photo electrodes were analyzed by scanning electron microscopy（SEM）, X-ray diffraction（XRD） and characterized accordingly. Moreover, the light harvesting and absorption properties were investigated via ultraviolet–visible diffuse reflectance spectrum（DRS）; photo degradation efficiency was investigated via analyzing the photo catalytic degradation of Rhodamine B under visible illumination（xenon light）. The performed analyses illustrated that Pd-MnO2 codoped particles were successfully deposited onto the surface of the TiO2 nanotube arrays;DRS results showed significant improvement in visible light absorption which was between400 and 700 nm. Finally, the photo catalytic degradation efficiency results of the designated organic pollutant（Rhodamine B） illustrated a superior photocatalytic（PC） efficiency of approximately 95% compared to the bare TiO2 NTAs, which only exhibited a photo catalytic degradation efficiency of approximately 61%, thus it indicated the significant enhancement of the light absorption properties of fabricated photo electrodes and their yield of UOH radicals.

Improving photoelectrochemical activity of dye sensitized solar cell by a bilayered electrode with an overlayer of mesoporous anatase TiO_2

For better performance of dye sensitized solar cells （DSSCs）, a bilayer structured electrode was constructed by employing a mesoporous anatase TiO2 overlayer above a commercial P25 TiO2 nanoparticles underlayer. The mesoporous anatase TiO2, prepared through a facile surfactant-assisted sol-gel process, possessed large pore size and well inter-connected network structure, both beneficial for dye adsorption and electron transfer. The dye adsorption capability of the mesoporous TiO2 was nearly twice that of the P25 counterpart. In the electrode, the mesoporous TiO2 film enhanced both dye adsorption and lightharvest, to increase photocurrent （Jsc） from 12.32 to 14.78 mA/cm^2. Compared to the single P25 TiO2 film, the synergy of the mesoporous TiO2 and the P25 TiO2 nanoparticle films in the electrode resulted in a 24% improvement in light-to-electricity conversion efficiency （η）. This bilayered electrode provides an alternative approach for further developing a photovoltaic device with better cell performance.

Electrolytic Fixation of CO_2 by Electrocarboxylation of RX on Nanocrystalline TiO_2-Pt Cathode

Electrolytic fixation of CO2 was investigated by electrocarboxylation of organic halides (RX), and four esters (I, II, III, IV) were obtained in moderate yields. Electrochemical reduction esterifications of RX in the presence of CO2 were carried out on nanocrystalline TiO2-Pt electrode. The electrochemical behavior of RX in the presence of CO2 was investigated by the technique of cyclic voltammetry, and the probable reaction mechanism was proposed.