arXiv subjects

Patrik Schmuki

Publications and source records attributed to Patrik Schmuki.

At least 55 records · Page 3Linked to original sources

arXiv2016

Use of Anodic TiO2 Nanotube Layers as Mesoporous Scaffolds for Fabricating CH3NH3PbI3 Perovskite-based Solid State Solar Cells

We optimize the deposition of CH3NH3PbI3 perovskite into mesoporous electrodes consisting of anodic TiO2 nanotube layers. By a simple spin coating approach, complete filling of the tube scaffolds is obtained, that leads to interdigitated perovskite structures in conformal contact with the TiO2 tube counterparts. Such assemblies can be used as solid state solar cells in hole-transporting material-free configuration, i.e., the tube scaffold serves as electron collector and blocking layer, while the perovskite acts as visible light absorber and hole transporting material. We show that the complete filling of the tube scaffold with the perovskite is essential to improve the solar cell efficiency.

cond-mat.mtrl-sci↗

arXiv2016

Transparent TiO2 Nanotubes Arrays Directly Grown on Quartz Glass Used in Front- and Back-Side Irradiation Configuration for Photocatalytic H2 Generation

In the present work we explore the front- and back-side performance of a photocatalytic platform consisting of self-organized TiO2 nanotube layers formed by complete anodization of Ti metal films evaporated on quartz slides. The adhesion and light transmission of the tube layers on the quartz surfaces are optimized by a suitable anodization procedure. After their growth, the nanotube arrays were converted into crystalline structures and sputter-coated with co-catalytic Pt nanoparticles. The optically transparent quartz substrates enable the use of the Pt-decorated tube layers for photocatalytic H2 generation under either front- or back-side illumination configurations. The nanotube films on quartz are characterized in view of their physico-chemical properties, including their light transmission features measured using different light sources. The results show that the front-side illumination under optimized factors, i.e., the amount of loaded co-catalyst, yields a maximized photocatalytic performance in terms of H2 generation.

cond-mat.mtrl-sci↗

arXiv2016

Open top anodic Ta3N5 nanotubes for higher solar water splitting efficiency

In the present work we grow self-organized Ta2O5 nanotube layers in a H2SO4/NH4F electrolyte at various elevated temperatures. Under optimized conditions we obtain 4 μm long nanotubes that are well adherent to the substrate and can be grown very homogenous over large surface areas. Moreover, the key advantage of this approach is that an open top morphology (initiation layer free) is obtained. After a suitable conversion treatment in NH3 atmosphere Ta3N5 nanotubes are obtained, that after (Co-Pi+Co(OH)x) modification provide, under AM 1.5G illumination conditions, a photoelectrochemical current response of 4.7 mA cm-2 at 1.23 V vs RHE.

cond-mat.mtrl-sci↗

arXiv2016

Photocatalytic H2 generation using dewetted Pt-decorated TiO2 nanotubes - Optimized dewetting and oxide crystallization by a multiple annealing process

In the present work we use TiO2 nanotube arrays, carrying a Pt coating that is optimally dewetted, as a photocatalyst to generate H2. In order to achieve a maximum H2-generation efficiency, on the one hand an ideal thermal dewetting of the Pt layer into nanoparticles is needed that requires an oxygen free heat treatment, and on the other hand an optimal crystallization of the TiO2 nanotubes into anatase with reduced defect density is achieved only by annealing in O2 containing environment. To overcome this issue, we combine adequate reducing and oxidizing conditions in a multiple annealing treatment, and obtain Pt-decorated anatase TiO2 nanotubes showing significantly enhanced photocatalytic H2 generation ability.

cond-mat.mtrl-sci↗

arXiv2016

One-dimensional Titanium Dioxide Nanomaterials: Nanotubes

In the present review we try to give a comprehensive and most up to date view to the field, with an emphasis on the currently most investigated anodic TiO2 nanotube arrays. We will first give an overview of different synthesis approaches to produce TiO2 nanotubes and TiO2 nanotube arrays, and then deal with physical and chemical properties of TiO2 nanotubes and techniques to modify them. Finally, we will provide an overview of the most explored and prospective applications of nanotubular TiO2.

cond-mat.mtrl-sci↗

arXiv2016

Molten o-H3PO4 - A New Electrolyte for the Anodic Synthesis of Self-Organized Oxide Structures: WO3 Nanochannel Layers and Others

We introduce the use of pure molten ortho-phosphoric acid (o-H3PO4) as an electrolyte for selforganizing electrochemistry. This electrolyte allows for the formation of self-organized oxide architectures (one-dimensional nanotubes, nanochannels, nanopores) on metals such as tungsten that up to now were regarded as very difficult to grow self-ordered anodic oxide structures. In this work, we show particularly the fabrication of thick, vertically aligned tungsten oxide nanochannel layers, with pore diameter of ca. 10 nm, and illustrate their potential use in some typical applications.

cond-mat.mtrl-sci↗

arXiv2016

High-Temperature Annealing of TiO2 Nanotube Membranes for Efficient Dye-Sensitized Solar Cells

We fabricate photo-anodes by transferring anodic TiO2 nanotube membranes in tube-top-down configuration on FTO glass, and use them for constructing frontside illuminated dye-sensitized solar cells. Prior to solar cell construction, the tube-based photo-anodes are crystallized at different temperatures (400-800°C), and the effects of tube electron transport properties on the photovoltaic performance of the solar cells are investigated. We show that improved solar cell efficiencies (up to ca. 8.0%) can be reached by high-temperature treatment of the tube membranes. Consistently with electron transport time measurements, remarkably enhanced electron mobility is enabled when tube membranes are crystallized at 600°C.

cond-mat.mtrl-sci↗

arXiv2016

Polydopamine-Coated TiO2 Nanotubes for Selective Photocatalytic Oxidation of Benzyl Alcohol to Benzaldehyde under Visible Light

TiO2 nanotube arrays grown by anodization were coated with thin layers of polydopamine as visible light sensitizer. The PDA-coated TiO2 scaffolds were used as photocatalyst for selective oxidation of benzyl alcohol under monochromatic irradiation at 473 nm. Benzaldehyde was selectively formed and no by-products could be detected. A maximized reaction yield was obtained in O2-saturated acetonitrile. A mechanism is proposed that implies firstly the charge carrier generation in polydopamine as a consequence of visible light absorption. Secondly, photo-promoted electrons are injected in TiO2 conduction band, and subsequently transferred to dissolved O2 to form oxygen radical anions. These radicals react with benzyl alcohol and lead to its selective dehydrogenation oxidation towards benzaldehyde.

cond-mat.mtrl-sci↗

arXiv2016

Free standing membranes to study the optical properties of anodic TiO2 nanotube layers

In the present work we investigate various optical properties (such as light absorption and reflectance) of anodic TiO2 nanotubes layers directly transferred as self-standing membranes onto quartz substrates. This allows investigation in a transmission geometry which provides significantly more reliable data than measurements on the metallic Ti substrate. Light transmission and reflectance measurements were carried out for layers of thicknesses varying from 1.8 to 50 micrometer, and the layers were investigated in their amorphous and crystalline form. A series of wavelength-dependent light attenuation coefficients are extrapolated and found to match the photocurrent vs. irradiation wavelength behavior. However, a feature specific to anodic nanotubes is that their intrinsic carbon content causes a sub-bandgap response that is proportional to the carbon contamination content in the TiO2 nanotubes. Overall the extracted data provide valuable basis and understanding for the design of photo-electrochemical devices based on TiO2 nanotubes.

cond-mat.mtrl-sci↗

arXiv2016

A Comparison of Anodic TiO2 Nanotube Membranes used for Front-side Illuminated Dye-Sensitized Solar Cells

In the present work we compare TiO2 nanotube lift-off strategies for the construction of front-side illuminated dye-sensitized solar cells (DSSCs). Anodic nanotube layers were detached from the metallic back contact by using different techniques and transferred onto an FTO substrate. We show that if we use an optimized potential step treatment to fabricate membranes, DSSC cell efficiencies can be significantly increased (>8%). This improved efficiency is ascribed to higher specific dye-loading and enhanced electron transport properties of optimally fabricated TiO2 nanotube membranes.

cond-mat.mtrl-sci↗

arXiv2016

Efficient Photocatalytic H2 Evolution: Controlled Dewetting-Dealloying to Fabricate Site-Selective High-activity Nanoporous Au Particles on Highly Ordered TiO2 Nanotube Arrays

Overlaid self-ordering processes: we form anodic self-organized TiO2 nanostumps and exploit them for self-ordering dewetting of Au-Ag sputtered films. This forms ordered particle configurations at tube top (crown position) or bottom (ground position). By dealloying we then form, from minimal amount of noble metal, porous Au nanoparticles that when in crown position allow for a drastically improved photocatalytic H2 production compared with nanoparticles produced by conventional dewetting processes.

cond-mat.mtrl-sci↗

arXiv2016

Noble metals on anodic TiO2 nanotubes mouths: Thermal dewetting of minimal Pt co-catalyst loading leads to significantly enhanced photocatalytic H2 generation

The least is the best. We introduce a technique to strongly reduce Pt use for photocatalytic hydrogen generation from TiO2 nanotubes. By site-selectively depositing thin layers of Pt only at the mouth of the nanotubes and by a subsequent thermal dewetting step, we achieve an outstanding photocatalytic improvement with minimal amounts of co-catalyst.

physics.chem-ph↗

arXiv2016

Single-walled TiO2 Nanotubes: Enhanced Carrier-transport Properties by TiCl4-Treatment

In the present work we report significant enhancement of the photoelectrochemical properties of self-organized TiO2 nanotubes by a combined de-coring of classic nanotubes followed by an appropiate TiCl4-treatment. We show that, except for the expected particle decoration, a key effect of the TiCl4 treatment is that the electron transport characteristics in TiO2 nanotubes can be drastically improved, e.g. we observe an enhancement of up to 70 % in electron transport times.

cond-mat.mtrl-sci↗

arXiv2016

Tungsten doping of Ta3N5-Nanotubes for Band Gap Narrowing and Enhanced Photoelectrochemical Water Splitting Efficiency

Ordered W-doped Ta2O5 nanotube arrays were grown by self-organizing electrochemical anodization of TaW alloys with different tungsten concentrations and by a suitable high temperature ammonia treatment, fully converted to W:Ta3N5 tubular structures. A main effect found is that W doping can decrease the band gap from 2 eV (bare Ta3N5) down to 1.75 eV. Ta3N5 nanotubes grown on 0.5 at% W alloy and modified with (CoOH)x as co-catalyst show ~33% higher photocurrents in photoelectrochemical (PEC) water splitting than pure Ta3N5.

cond-mat.mtrl-sci↗

arXiv2016

Suspended Pt nanoparticles over TiO2 nanotubes for enhanced photocatalytic H2 evolution

In the present work we introduce a technique to form a photocatalyst, based on Pt nanoparticles suspended over the mouth of TiO2 nanotubes. These structures are obtained by the decoration of the top end of highly ordered TiO2 nanotubes with a web of TiO2 nanofibrils, followed by sputter deposition of a minimum amount of Pt. A subsequent thermal dewetting step forms 3-6 nm-sized Pt nanoparticles along the nanofibrils. These structures, when compared to conventional Pt decoration techniques of TiO2 nanotubes, show a strongly enhanced photocatalytic H2 evolution efficiency.

physics.chem-ph↗

arXiv2016

Aligned metal oxide nanotube arrays: key-aspects of anodic TiO2 nanotube formation and properties

Over the past ten years, self-aligned TiO2 nanotubes have attracted tremendous scientific and technological interest due to their anticipated impact on energy conversion, environment remediation and biocompatibility. In the present manuscript, we review fundamental principles that govern the self-organized initiation of anodic TiO2 nanotubes. We start with the fundamental question: Why is self-organization taking place? We illustrate the inherent key mechanistic aspects that lead to tube growth in various different morphologies, such as rippled-walled tubes, smooth tubes, stacks and bamboo-type tubes, and importantly the formation of double-walled TiO2 nanotubes versus single-walled tubes, and the drastic difference in their physical and chemical properties. We show how both double- and single-walled tube layers can be detached from the metallic substrate and exploited for the preparation of robust self-standing membranes. Finally, we show how by selecting the right growth approach to TiO2 nanotubes specific functional features can be significantly improved, e.g., an enhanced electron mobility, intrinsic doping, or crystallization into pure anatase at extremely high temperatures can be achieved. This in turn can be exploited in constructing high performance devices based on anodic TiO2 in a wide range of applications.

cond-mat.mtrl-sci↗

arXiv2016

Aminated TiO2 nanotube as a Photoelectrochemical Water Splitting photoanode

The present work reports on the enhancement of TiO2 nanotubes photoelectrochemical water splitting rate by decorating the nanostructure with an amine layer in a hydrothermal process using diethylenetriamine (DETA). The aminate coated TiO2 tubes show a stable improvement of the photoresponse in both UV and visible light spectrum and under hydrothermal conditions, 4-fold increase of the photoelectrochemical water splitting rate is observed. From intensity modulated photocurrent spectroscopy (IMPS) measurements significantly faster electron transport times are observed indicating a surface passivating effect of the N-decoration.

cond-mat.mtrl-sci↗

arXiv2016

Ar+-ion Bombardment of TiO2 Nanotubes Creates Co-catalytic Effect for Photocatalytic Open Circuit Hydrogen Evolution

In the present work, extended Argon ion bombardment was used to modify anatase TiO2 nanotube (NTs) layers. In situ X-ray photoelectron spectroscopy revealed a high content of sub-oxide formed (Ti3+, Ti2+ states) in the nanotube layers. These samples were tested for their ability to show open-circuit photocatalytic hydrogen evolution. We found for UV (cw laser 325nm) illumination as well as for AM1.5 conditions, a strongly enhanced H2 evolution activity in absence of the usual noble metal-nanoparticle decoration. We conclude therefore that these sub-oxide states can play an important role in the activation of TiO2 nanotubes - namely as a H2 evolution co-catalyst.

cond-mat.mtrl-sci↗