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Tantalum doped rutile nanorods were hydrothermally grown on FTO substrates using a new seeding approach. This approach allows the incorporation of high concentrations of up to 4.8 at% tantalum as active doping and results in a significant enhancement of photoelectrochemical water splitting rate (1.8 mA/cm2 at a potential of +1.5 V vs RHE) which corresponds to ca. 1% photocurrent conversion efficiency under AM 1.5, 100 mW/cm2 simulated sunlight irradiation.

In this work we describe the synthesis and electrochemical properties of nitridated hierarchical TiO$_2$ nanotubes as an electrode for supercapacitors. The hierarchical TiO$_2$ nanostructures are formed by a controlled layer-by-layer TiO2 nanoparticle decoration on self-organized spaced TiO$_2$ nanotubes. These structures are then annealed in NH$_3$ atmosphere at elevated temperature to convert the material to a nitride structure -- this drastically enhances their electron-transport properties. The areal capacitance of hierarchical structures can be tuned by changing the number of decorated TiO$_2$ nanoparticle layers. The capacitance enhancement of the hierarchical structures reaches a maximum when the surface area through nanoparticle deposition is highest and the conductivity via nitridation is optimized.

Over the past ten years, self-aligned TiO

In this research, we investigate the effect of alkali metal cations including Li, Na and Cs in hydrothermal solution on the morphology, stability, and photoactivity of nanostructured TiO2 nanoflakes as a photoanode. The TiO2 nanoflakes are formed through hydrothermal treatment of Ti foil in 1.0 M LiOH, NaOH or CsOH at 100 °C for 3 h. By subsequent thermal reduction of the structure in an optimized Ar/H2 environment, conductive TiO2 nanoflakes were formed. The reduction treatment remarkably improves the photocurrent density of the TiO2 nanoflakes and has the highest impact on the sample treated in the NaOH alkali solution. For the nanoflakes produced in NaOH alkali solution, the bandgap is shifted to a lower value and the structure shows the most stable morphology after thermal treatment compared to nanoflakes formed in other alkali solutions. Such reduced hydrothermally treated nanoflakes formed in NaOH can generate a photocurrent density of approximately 1 mA/cm−2 vs. Ag/AgCl in 1.0 M KOH solution, which is six times higher than for pristine TiO2.

Anodic TiO

Recently, sodium ion batteries (SIBs) have been widely investigated as one of the most promising candidates for replacing lithium ion batteries (LIBs). For SIBs or LIBs, designing a stable and uniform solid electrolyte interphase (SEI) at the electrode–electrolyte interface is the key factor to provide high capacity, long‐term cycling, and high‐rate performance. In this paper, it is described how a remarkably enhanced SEI layer can be obtained on TiO2 nanotube (TiO2 NTs) arrays that allows for a strongly improved performance of sodium battery systems. Key is that a Li+ pre‐insertion in TiO2 NTs can condition the SEI for Na+ replacement. SIBs constructed with Li‐pre‐inserted NTs deliver an exceptional Na+ cycling stability (e.g., 99.9 ± 0.1% capacity retention during 250 cycles at a current rate of 50 mA g−1) and an excellent rate capability (e.g., 132 mA h g−1 at a current rate of 1 A g−1). The key factor in this outstanding performance is that Li‐pre‐insertion into TiO2 NTs leads not only to an enhanced electronic conductivity in the tubes, but also expands the anatase lattice for facilitated subsequent Na+ cycling.

Anodically-grown arrays of TiO2 nanocavities[1] are used as substrate for solid state dewetting of Au thin films (≤ 20 nm-thick).[2,3] The resulting Au nanoparticle-decorated structures are explored as a photocatalytic platform for the reduction and scavenging of Hg(II) ions in aqueous solutions under solar illumination.[4] The presence of the dewetted Au nanoparticles leads to a strong improvement of the photocatalytic Hg(II) reduction performance. Different reaction pathways are recognized for the Hg(II) abatement, which depend on parameters such as the Hg ion concentration, the Au nanoparticle size/loading, and the presence/absence of chloride ions and their concentration. ICP-MS analysis of photocatalytically treated water streams confirms that under any experimental condition explored the removed Hg(II) is always accumulated on the photocatalyst surface. Interestingly, in the presence of chlorides (to simulate contaminated sea water), and with relatively high Hg concentrations (10 ppm) and Au nanoparticle loadings (Au film initial thickness ~ 20 nm), a massive growth of calomel (Hg2Cl2) nanowires is observed. The nature of the photo-produced nanowires was confirmed by EDS and XPS analysis. The Hg2Cl2 nanowires nucleate at the surface of the Au nanoparticles, and their morphology (width, length, aspect-ratio) can be tuned by adjusting the Au nanoparticle size and illumination time. On the other hand, in the absence of chlorides and/or at lower Hg(II) concentrations, Hg removal occurs via accumulation on the photocatalyst surface through the formation of AuHg alloy (amalgam) nanostructures. Both mechanisms lead to an effective abatement of Hg: under solar light illumination, the scavenging process can lead to a Hg removal efficiency as high as 90% after 24 h. Regeneration of the Hg-loaded exhaust photocatalyst can be performed by photo-electrochemical anodic stripping, which converts the deposited Hg(0)/Hg(I) into soluble Hg(II), allowing for the accumulation of the scavenged Hg into small volumes of concentrated wastes. After four photocatalyst use/regeneration cycles, only a 10% decrease of activity was observed. Besides the relevance of the photocatalytic results for water remediation technologies, our findings can also provide reliable nanostructuring tools for the templated synthesis of amalgam nanoparticles of tunable composition and size, or for the controlled growth of calomel nanowires for electro-analytical or sensing applications. [1] J. E. Yoo, K. Lee, M. Altomare, E. Selli, P. Schmuki, Angew. Chemie Int. Ed. 2013, 52, 7514–7517. [2] C. V. Thompson, Annu. Rev. Mater. Res. 2012, 42, 399–434. [3] M. Altomare, N. T. Nguyen, P. Schmuki, Chem. Sci. 2016, 7, 6865–6886. [4] D. Spanu, A. Bestetti, H. Hildebrand, P. Schmuki, M. Altomare, S. Recchia, Photochem. Photobiol. Sci. 2019, 18, 1046–1055.

Titanium dioxide (TiO2) is the most investigated semiconductor in photocatalysis, but the photocatalytic performance can be further improved by rational design of the material as nanostructure with special surface and structural properties. In this chapter, we discuss methods for site-selective decoration of anodic TiO2 nanotube (NT) arrays, particularly to introduce stable defects and investigate the mechanism for enhanced activity and stability of these noble metal–free photocatalysts. The investigated methods include proton implantation and nitrogen implantation into the TiO2 NTs and decoration of alternative cocatalysts (e.g., molybdenum-based cocatalysts). Such modification on TiO2 NT layers leads to the creation of efficient photocatalysts for H2 evolution, which is ascribed to the synergistic effect of light harvesting by TiO2 NTs coupled with cocatalytic centers atop the tube layers. The described methods for selective decoration of TiO2 NTs can be further extended and potentially applied to the activation of a range of one-dimensional (1D) semiconductor materials.

The anodic oxidation of niobium is investigated in pure molten ortho-phosphoric acid (o-H3PO4). At applied potentials in the 2.5–60 V range and for electrolyte temperatures in the 60–110 °C range, porous niobium oxide layers are formed. Pore ordering and morphology depend on the anodization voltage, time and temperature, i.e. the anodic oxide develops different morphologies depending on low- or high-field anodizing conditions. At 100 °C and low voltages, e.g. ≤ 5 V, vertically oriented, amorphous oxide nanopores with cylindrical shape (“nanochannels”) grow with an average diameter of 5–8 nm. Higher voltages (10–20 V) lead to a less ordered pore morphology, resembling a “fish bone” structure. At 40–60 V, and after a sufficiently long anodization time (≥30 min), an orthorhombic Nb2O5 hierarchical structure forms that shows a bimodal pore size distribution with some 100 nm wide main pores that branch out into ∼ 10 nm wide side nanochannels. A partial crystallization of the anodic oxide is observed at high voltages (≥40 V). We propose that this is due to a high field-induced crystallite nucleation in the barrier oxide at the oxide/metal interface. With time, the crystalline oxide is incorporated in the porous layer. The main pores, partially crystalline and hence more stable in the anodizing electrolyte, result from the gradual dissolution of the amorphous side nanochannels.

In this work, single crystalline $\alpha$-Fe$_2$O$_3$ nanoflakes (NFs) are formed in a highly dense array by Au seeding of a Fe substrate by a thermal oxidation technique. The NFs are conformally decorated with a thin FeOOH cocatalyst layer. Photoelectrochemical (PEC) measurements show that this photoanode with the $\alpha$-Fe$_2$O$_3$/FeOOH NFs rooted on the Au/Fe structure exhibits a significantly enhanced PEC water oxidation performance compared to the plain $\alpha$-Fe$_2$O$_3$ nanostructure on the Fe substrate. The $\alpha$-Fe$_2$O$_3$/FeOOH NFs on Au/Fe photoanode yields a photocurrent density of 3.1 mA cm-2 at 1.5 VRHE, and a remarkably low onset potential of 0.5-0.6 VRHE in 1 M KOH under AM 1.5G (100 mW cm-2) simulated sunlight illumination. The enhancement in PEC performance can be attributed to a synergistic effect of the FeOOH top decoration and Au under-layer. While FeOOH facilitates hole transfer at the interface of electrode/electrolyte, the Au layer provides a sink for the electron transport to the back contact: this leads overall to a drastically improved charge-separation efficiency in the single crystalline $\alpha$-Fe$_2$O$_3$ NF photoanode.

ACS catalysis 10, 8293 - 8302 (2020). doi:10.1021/acscatal.0c01373, Cu- or Ni-decorated semiconductors represent a potential low-cost alternative to noble-metal-modified photocatalysts. Even more effective are bimetallic NiCu nanoparticles, which can provide a remarkable photocatalytic H$_{2}$ evolution enhancement compared to single-element Cu or Ni systems. The main concern of such alloyed co-catalysts is their activity with respect to alteration of their elemental composition and oxidation state over reaction time. Ex situ characterization techniques provide controversial interpretations of the co-catalytic role of the individual elements. Hypotheses such as the in situ reduction of ���native��� Ni or Cu species during photocatalysis, the oxidation of metallic Cu or Ni into oxides or hydroxides, or the formation of p���n junctions or core/shell structures have been proposed. Herein, we present an operando X-ray absorption spectroscopy study of a NiCu���TiO$_{2}$ system under UV light illumination in ethanol���water solutions, i.e., under photocatalytic H$_{2}$ evolution conditions. The experimental approach allows for monitoring in real time chemical changes that take place in the co-catalyst under intermittent illumination, i.e., under light on���off cycles. We show that while Ni and Cu are partially oxidized in the as-formed NiCu co-catalyst (air-formed surface oxides or hydroxides) and undergo partial dissolution in the liquid phase under dark conditions, such Ni and Cu oxidized and dissolved species are reduced/redeposited as a bimetallic NiCu phase at the TiO$_{2}$ surface under illumination. The dissolution/redeposition mechanism is triggered by TiO$_{2}$ conduction band electrons. We not only prove a UV-light-induced healing of the NiCu co-catalyst but also unambiguously demonstrate that the species responsible for the strongly enhanced photocatalytic H$_{2}$ evolution of NiCu nanoparticles are the metallic states of Ni and Cu., Published by ACS, Washington, DC

Pt nanoparticles are typically decorated as co-catalyst on semiconductors to enhance the photocatalytic performance. Due to the low abundance and high cost of Pt, reaching a high activity with minimized co-catalyst loadings is a key challenge in the field. We explore a dewetting-dealloying strategy to fabricate on TiO2 nanotubes nanoporous Pt nanoparticles, aiming at improving the co-catalyst mass activity for H2 generation. For this, we sputter first Pt-Ni bi-layers of controllable thickness (nm range) on highly ordered TiO2 nanotube arrays, and then induce dewetting-alloying of the Pt-Ni bi-layers by a suitable annealing step in a reducing atmosphere: the thermal treatment causes the Pt and Ni films to agglomerate and at the same time mix with each other, forming on the TiO2 nanotube surface metal islands of a mixed PtNi composition. In a subsequent step we perform chemical dealloying of Ni that is selectively etched out from the bimetallic dewetted islands, leaving behind nanoporous Pt decorations. Under optimized conditions, the nanoporous Pt-decorated TiO2 structures show a>6 times higher photocatalytic H2 generation activity compared to structures modified with a comparable loading of dewetted, non-porous Pt. We ascribe this beneficial effect to the nanoporous nature of the dealloyed Pt co-catalyst, which provides an increased surface-to-volume ratio and thus a more efficient electron transfer and a higher density of active sites at the co-catalyst surface for H2 evolution.

Noble metal cocatalysts are conventionally a crucial factor in oxide-semiconductor-based photocatalytic hydrogen generation. In the present work, we show that optimized high-temperature hydrogenation of commercially available strontium titanate (SrTiO3) powder can be used to engineer an intrinsic cocatalytic shell around nanoparticles that can create a photocatalyst that is highly effective without the use of any additional cocatalyst for hydrogen generation from neutral aqueous methanol solutions. This intrinsic activation effect can also be observed for SrTiO3[100] single crystal as well as Nb-doped SrTiO3 (100) single crystal. For all types of SrTiO3 samples (nanopowders and either of the single crystals), hydrogenation under optimum conditions leads to a surface-hydroxylated layer together with lattice defects visible by transmission electron microscopy, electron paramagnetic resonance (EPR), and photoluminescence (PL). Active samples provide states in a defective matrix -- this is in contrast to the inactive defects formed in other reductive atmospheres. In aqueous media, active SrTiO3 samples show a significant negative shift of the flatband potential (in photoelectrochemical as well as in capacitance data) and a lower charge-transfer resistance for photoexcited electrons. We therefore ascribe the remarkable cocatalyst-free activation of the material to a synergy between thermodynamics (altered interface energetics induced by hydroxylation) and kinetics (charge transfer mediation by suitable Ti3+ states).

In this work, we report on the electrochemical behavior of nitrided spaced TiO$_2$ nanotubes conformally coated with a nanocrystalline Nb$_2$O$_5$ layer and find for these hierarchical structures an excellent supercapacitor performance. Highly aligned conductive 1D electrodes were obtained by a three step process: i) growth of self-organized nanotubes with defined and adjustable intertube spacing, ii) conformal Nb$_2$O$_5$ decoration in the tube interspace (while providing full electrolyte access to the entire active area), and iii) high temperature nitridation. Key is the growth of a nanotube array with regular tube-to-tube interspacing that enables an optimized decoration with secondary materials such as Nb$_2$O$_5$. We observe an increase in electrode capacitance from 158 $\mu$F cm-2 for bare TiO$_2$ NTs, to 1536 $\mu$F cm-2 for TiO$_2$/Nb$_2$O$_5$ NTs, to finally 37 mF cm-2 for Nb$_2$O$_5$ decorated and then nitrided nanotubes. This drastic increase can be ascribed firstly to the defined spacing established between the tube arrays that then allows for a conformal coating with a secondary active coating. Secondly, nitridation causes a drastic increase of the electron conductivity of the entire scaffold and thus reduces resistive losses.

In this work, we describe a simple anodization process of titanium in a hot phosphoric acid/ethylene glycol electrolyte that forms a hierarchically structured photocatalytically active TiO2 layer that consists directly of anatase nanocrystallites. Such anodic layers show, without any annealing, a high photocatalytic degradation activity for AO7 (an azo‐dye used as model pollutant) that is higher than the activity of comparable fully crystallized TiO2 nanotube layers. Furthermore, the hierarchically structured layers have a remarkable mechanical bending stability. These features make these novel anodic layers highly promising for applications in flexible substrate based photocatalytic devices.

The need to satisfy the growing global population’s enormous energy demands is a major challenge for modern societies. Photoelectrochemical (PEC) water splitting (WS) is seen as a leading strategy for producing an extremely promising renewable store of energy – hydrogen (H2). However, PEC-WS is a complex process involving several sequential physicochemical reaction steps including light absorption, separation of photoexcited charges, and surface redox reactions. At present, FeO-based semiconductors represent a unique class of materials known to exhibit very high performance in all these processes. This review summarizes and critically discusses the major components of PEC-WS systems incorporating FeO-based light-harvesting systems, and outlines the progress that has been made, particularly over the last decade. Emphasis is placed on materials used as photoanodes (including hematite and nonhematite iron oxides, spinel iron ferrites, and pseudobrookite iron titanates) as well as materials used as cocatalysts and passivation layers – notably iron hydroxyoxides and their composites. We discuss strategies for overcoming the main limitations of the aforementioned materials via nanostructuring, elemental doping, surface decoration, and the formation of advanced hybrid nanoarchitectures. Finally, we use this knowledge to present a critical overview of the field and the future prospects of Fe-O semiconductors in PEC-WS applications.

Self-standing TiO$_2$ nanotube layers in the form of membranes are fabricated by self-organizing anodization of Ti metal and a potential shock technique. The membranes were then decorated by sputtering different Pt amounts i) only at the top, ii) only at the bottom or iii) at both top and bottom of the tube layers. The Pt-decorated membranes are transferred either in tube top up or in tube top down configuration onto FTO slides and investigated after crystallization as photocatalysts for H$_2$ generation using either front or back-side light irradiation. Double-side Pt-decoration of the tube membranes leads to higher H$_2$ generation rates (independent of tube and light irradiation configuration) compared to membranes decorated at only one side with similar overall Pt amounts. The results suggest that this effect is not ascribed to the overall amount of Pt cocatalyst as such but rather to its distribution at both tube extremities. This leads to optimized light absorption and electron diffusion/transfer dynamics: the central part of the membranes act as light harvesting zone and electrons therein generated can diffuse towards the Pt/TiO$_2$ active zones (tube extremities) where they can react with the environment and generate H$_2$ gas.

Photocatalytic $H_2$ evolution reactions on pristine TiO$_2$ is characterized by low efficiencies due to trapping and recombination of charge carriers, and due to a sluggish kinetics of electron transfer. Noble metal (mainly Pt, Pd, Au) nanoparticles are typically decorated as cocatalyst on the TiO$_2$ surface to reach reasonable photocatalytic yields. However, owing to the high cost of noble metals, alternative metal cocatalysts are being developed. Here we introduce an approach to fabricate an efficient noble metal free photocatalytic platform for $H_2$ evolution based on alloyed NiCu cocatalytic nanoparticles at the surface of anodic TiO$_2$ nanotube arrays. NiCu bilayers are deposited onto the TiO$_2$ nanotubes by plasma sputtering. A subsequent thermal treatment is carried out that leads to dewetting, that is, owing to surface diffusion the Ni and Cu sputtered layers simultaneously mix with each other and split into NiCu nanoparticles at the nanotube surface. The approach allows for a full control over key features of the alloyed nanoparticles such as their composition, work function and cocatalytic ability towards $H_2$ generation. Dewetted-alloyed cocatalytic nanoparticles composed of equal Ni and Cu amounts not only are significantly more reactive than pure Ni or Cu nanoparticles, but also lead to $H_2$ generation rates that can be comparable to those obtained by conventional noble metal (Pt) decoration of TiO$_2$ nanotube arrays.

The use of single atoms (SAs) has become a highly investigated topic in heterogeneous catalysis, electrocatalysis, and most recently also in photocatalysis. In the field of photocatalysis, Pt SAs on TiO2 have been reported to be a highly efficient co‐catalyst in solar H2 production. Herein, the deposition of Pt SAs and nanoparticles on titania nanosheets is investigated. In particular, the Pt species responsible for the high co‐catalytic activity using a cyanide leaching process is elucidated. It is shown that neither Pt0 species nor the majority of Pt SAs do significantly contribute to the co‐catalytic activity of platinum on TiO2. In fact, >90% of the Pt of a standard deposition are non‐active and can be removed by cyanide leaching without activity loss—as a consequence, the remaining Pt SAs amount to a remarkable turnover frequency of 4.87 × 105 h−1 for H2 evolution.

Hematite-based photoanodes were used for the photoelectrocatalysed batch oxidation of As(III) in water at pH 7 and 10. Tests were carried out at different As(III) initial concentrations, ranging from 150 μg/L to 30 mg/L. With no pre-treatments, an initial inactive period of 40–50 min was always observed at the beginning of every test. This initial inactive period is completely removed by a surface modification of surface active sites induced by a pre-polarisation at 800 mV (vs. Ag/AgCl). The water splitting active sites related to the Fe(III)-Fe(IV) redox couple were proved to be not active towards As(III) oxidation. The modifications induced by the anodic prepolarisation were deeply studied: no evidence of the formation of surface highly oxidised iron sites (Fe(V) or Fe(VI)) and/or of highly reactive oxygen vacant sites emerges from XPS analysis. Rather, all collected characterisation data support the conclusion that more reactive terminal oxygen species are necessary for As(III) oxydation. The As(III) abatement reaction was modelled by two subsequent first order kinetics in As(III), independently from the initial As(III) concentration: this behaviour was explained suggesting that the highly reactive sites, being formed after prepolarisation, are gradually depleted during the reaction. As this reaction was proved to be very sensitive to the presence of highly reactive iron sites, its utilisation as a probe reaction to study hematite photoanodes is suggested.

In the present work, we investigate two distinctly different anodic TiO2 nanotubular morphologies, spaced and close-packed arrays. While the close-packed tubular arrays are formed in ethylene glycol, spaced NTs, which have a regular gap between individual nanotubes, grow in a diethylene glycol or dimethyl sulfoxide based electrolyte. Depending on the electrolyte used for anodization, the morphology, crystal structure and chemical composition of the resulting nanotubular layer vary from one another. This influences the electrochemical and photoelectrochemical activity of nanotubes. Overall, we find that spaced NTs not only can provide enhanced charge transfer characteristics but also can show beneficial light absorption characteristics when used as a photo or light harvesting electrode.

Fe2O3 polyhedrons are one of the most promising morphologies for photoelectrochemical water splitting. In spite of recent reports on the successful synthesis of various Fe2O3 polyhedrons, the fabrication of defined photoelectrodes by anchoring the polyhedron in a suitable configuration remains a great challenge. Herein, we introduce a synthetic strategy to prepare Fe2O3 dodecahedrons with high-index {112} facets directly anchored on a one dimensional Fe2O3 nanoflake ({110} facets) electrode. Key is that the Fe2O3 nanoflakes act as seeds for the initiation of the growth of dodecahedral nanocrystals from an iron nitrate solution. The initial single crystals consist of Fe3O4 with exposed {110} basal surfaces that then in a thermal step can be converted to hematite with {112} facets. The resulting single crystal (bi-crystal) hematite photoanode demonstrates a high efficiency for solar water splitting with an excellent photoresponse due to the synergistic effects of direct grafting of the light harvesting and reactive polyhedron and the 1D transport geometry. Under optimized conditions the hematite polyhedrons on nanoflake-structure show photocurrent densities of 2.4 mA cm−2 at 1.23 VRHE and 3.5 mA cm−2 at 1.5 VRHE under AM 1.5 G simulated sunlight.

In this paper we prepare facetted “black” TiO2 nanotube arrays (NTAs) with a bamboo-type structure which exhibits an enhanced performance for open-circuit H2 generation without the use of any noble metal co-catalyst. By applying positive and negative voltages alternatively during electrochemical TiO2 nanotube formation, not only a bamboo structure can be formed but tubes are reduced in the cathodic cycle. After a rapid annealing treatment of these tubes in air at 500 ºC for 10 s, TEM shows that the bamboo rings (knots) provide (001) facets preferentially located at the knot, while (101) planes prevail on the smooth part of tube between knots. The short annealing time keeps co-catalytically active centers (Ti3+/oxygen vacancy (VO)) still preserved in the TiO2 NTAs. The results of intensity modulated photocurrent spectroscopy (IMPS) and open-circuit potential (VOC) measurements indicate that these faceted and reduced TiO2 nanotube arrays provide an efficient separation and reaction of photo-generated charge carriers, and this leads to an improved photocatalytic H2 evolution performance.

In this work we study the depth composition of anodic TiO2 nanotube layers. We use elemental depth profiling with Glow Discharge Optical Emission Spectroscopy and calibrate the results of this technique with X-ray photoelectron spectroscopy (XPS) and energy dispersive spectroscopy (EDS). We establish optimized sputtering conditions for nanotubular structures using the pulsed RF mode, which causes minimized structural damage during the depth profiling of the nanotubular structures. This allows to obtain calibrated sputter rates that account for the nanotubular “porous” morphology. Most importantly, sputter-artifact free compositional profiles of these high aspect ratio 3D structures are obtained, as well as, in combination with SEM, elegant depth sectional imaging.

Au and Pt do not form homogeneous bulk alloys as they are thermodynamically not miscible. However, we show that anodic TiO2 nanotubes (NTs) can in situ be uniformly decorated with homogeneous AuPt alloy nanoparticles (NPs) during their anodic growth. For this, a metallic Ti substrate containing low amounts of dissolved Au (0.1 atom %) and Pt (0.1 atom %) is used for anodizing. The matrix metal (Ti) is converted to oxide, whereas at the oxide/metal interface direct noble metal particle formation and alloying of Au and Pt takes place; continuously these particles are then picked up by the growing nanotube wall. In our experiments, the AuPt alloy NPs have an average size of 4.2 nm, and at the end of the anodic process, these are regularly dispersed over the TiO2 nanotubes. These alloyed AuPt particles act as excellent co-catalyst in photocatalytic H2 generation, with a H2 production rate of 12.04 μL h–1 under solar light. This represents a strongly enhanced activity as compared to TiO2 NTs decorated with mon...

Over the past years, α-Fe2 O3 (hematite) has re-emerged as a promising photoanode material in photoelectrochemical (PEC) water splitting. In spite of considerable success in obtaining relatively high solar conversion efficiency, the main drawbacks hindering practical application of hematite are its intrinsically hampered charge transport and sluggish oxygen evolution reaction (OER) kinetics on the photoelectrode surface. In the present work, we report a strategy that synergistically addresses both of these critical limitations. Our approach is based on three key features that are applied simultaneously: i) a careful nanostructuring of the hematite photoanode in the form of nanorods, ii) doping of hematite by Sn4+ ions using a controlled gradient, and iii) surface decoration of hematite by a new class of layered double hydroxide (LDH) OER co-catalysts based on Zn-Co LDH. All three interconnected forms of functionalization result in an extraordinary cathodic shift of the photocurrent onset potential by more than 300 mV and a PEC performance that reaches a photocurrent density of 2.00 mA cm-2 at 1.50 V vs. the reversible hydrogen electrode.

Self-organized TiO2 nanotube arrays can be grown under a wide range of electrochemical conditions. In the present work, we evaluate the occurrence of spacing between tubes and the connection of this effect to organization of tubes on two-size scales. The results show that tube-spacing is initiated in the very early stages of anodization between individual pore morphologies. Furthermore, the spacing, as well as the organization on two-size scales can be controlled by changing the anodization conditions, e.g., electrolyte composition, applied voltage and temperature. Namely, adjustment of H2O content, electrode temperature and voltage can lead to spaced nanotubes, and allow to control spacing. Finally, we draw conclusions on the possible mechanism relevant to the growth of spaced tubes.

Compared to many other metal oxides, anatase TiO2 shows relatively lower reactivity toward carboxylic acid anchor groups. The latter is crucial for applications, for example, in dye-sensitized solar cells (DSSCs), where the most used dyes bind to the metal oxide surface through carboxylic acid terminations. To improve the surface reactivity, metal-phosphate bilayers of Ni or Co were synthesized on anatase TiO2 compact oxide and nanotubes. In both cases, time-of-flight secondary ion mass spectrometry (ToF-SIMS) and X-ray photoelectron spectroscopy (XPS) results showed that the bilayers were successfully formed and that the phosphate layer works as an intermediate between TiO2 and the other species. ToF-SIMS depth profiles of modified nanotubes showed that Ni and Co are present through the whole tube length and reduce in content after heat treatment, in agreement with XPS results. Phosphate groups, on the other hand, are more present in the tubes' depth, and their content on the surface is reduced upon exposure to temperature. The reactivity of the modified surfaces toward carboxylic acid-terminated molecules, as stearic acid and Ru-based N719 dye, was evaluated. Contact angle measurements together with dye desorption experiments demonstrated that the Co-phosphate bilayers heat-treated at 300 °C resulted in the largest enhancement compared to the reference. Bilayer-modified compact anatase TiO2 and anatase TiO2 nanotubes were utilized as photoanodes in DSSCs. An increase in efficiency was observed for all modified electrodes with phosphate-Co treatment, leading to the highest JSC values and an efficiency improvement of 48%.

Anodic TiO2 nanotube membranes of various thicknesses (1.5–60 μm) fixed on FTO slides were site-selectively decorated with Pt nanoparticles at only their upper extremity. Their photocatalytic H2 evolution ability (with and without Pt) is investigated under UV light (325 nm) illumination through the FTO slide. The irradiation side is opposite to the Pt decorations in order to avoid Pt shading effects. This design is key to study the H2 evolution in relation to membrane thickness, light absorbance, and electron diffusion length in the nanotubes. The Pt decoration improves the H2 evolution, and the photocatalytic enhancement, quantified as ratio of H2 evolution rate with Pt vs. that without Pt, varies with the membrane thickness. The highest photocatalytic enhancement is for 5-10 μm-long nanotubes, owing to maximized photon harvesting and efficient electron trapping/transfer to reactants. This is enabled by a short pathway of electron diffusion towards Pt. The photocatalytic enhancement drops dramatically for membrane >30 μm while membranes of intermediate lengths (∼10–30 μm) show similar photocatalytic enhancement. This can be ascribed to an electron diffusion length in Pt-TiO2 nanotubes of 20–30 μm.

In the present work we grow anodic TiO2 nanotube layer with a tube diameter > 500 nm and an open tube mouth. We use this morphology in dye-sensitized solar cells (DSSCs) and show that these tubes allow the construction of hybrid hierarchical photoanode structures of nanotubes with a defined and wall-conformal TiO2 nanoparticle decoration. At the same time, the large diameter allows the successful establishment of an additional (insulating) blocking layer of SiO2 or Al2O3 on the tube wall. We show that this combination of hierarchical structure and blocking layer significantly enhances the solar cell efficiency by suppressing recombination reactions. In such a DSSC structure, the solar cell efficiency under back side illumination with AM1.5 illumination is enhanced from 3% for the neat tube to 5 % for the hierarchical structure, to 7 % when additionally a blocking layer is attached.

The efficiency of photoelectrochemical (PEC) water splitting of semiconductors is mainly restricted by the sluggish kinetics of the oxygen evolution reaction dominated by photogenerated holes. Herein, we demonstrate that with the assistance of photon-induced surface plasmon resonance excitation of Au nanoparticles, the iron oxyhydroxides (FeOOH) cocatalysts could serve as a unique “hole-depletion” layer for significantly promoting the PEC performance of single crystalline α-Fe2O3 photoanodes. The photogenerated holes can be efficiently extracted from α-Fe2O3 nanoflake to FeOOH layer, and promptly depleted by the injected hot-electrons from Au nanoparticles, while the hot-holes left behind on Au participate in the oxygen evolution reaction. Accordingly, the synergy of charge separation and hole transfer could be efficiently improved by the surface plasmon excitation on Au nanoparticles. As a result, the photocurrent density for the Fe2O3/FeOOH/Au photoelectrode without additional doping reaches up to 3.2 mA cm−2 at 1.23 VRHE, and 6.5 mA cm−2 at 1.6 VRHE, with a low onset potential of 0.6 VRHE under AM 1.5 G simulated sunlight, which is 2.5 and 5 times higher than for FeOOH modified and pristine α-Fe2O3 photoanodes, respectively. These results thus provide the basic of a new concept and strategy toward the design of more efficient PEC water splitting systems.

Photocatalytic reactions on TiO2 have recently gained an enormous resurgence because of various new strategies and findings that promise to drastically increase efficiency and specificity of such reactions by modifications of the titania scaffold and chemistry. In view of geometry, in particular, anodic TiO2 nanotubes have attracted wide interest, as they allow a high degree of control over the separation of photogenerated charge carriers not only in photocatalytic reactions but also in photoelectrochemical reactions. A key advantage of ordered nanotube arrays is that nanotube modifications can be embedded site specifically into the tube wall; that is, cocatalysts, doping species, or junctions can be placed at highly defined desired locations (or with a desired regular geometry or pattern) along the tube wall. This allows an unprecedented level of engineering of energetics of reaction sites for catalytic and photocatalytic reactions, which target not only higher efficiencies but also the selectivity of reactions. Many recent tube alterations are of a morphologic nature (mesoporous structures, designed faceted crystallites, hybrids, or 1D structures), but a number of color-coded (namely, black, blue, red, green, gray) modifications have attracted wide interest because of the extension of the light absorption spectrum of titania in the visible range and because unique catalytic activity can be induced. The present Perspective gives an overview of TiO2 nanotubes in photocatalysis with an emphasis on the most recent advances in the use of nanotube arrays and discusses the underlying concepts in tailoring their photocatalytic reactivity.

In the present work, we introduce a technique to achieve rapid growth of self-ordered anodic nanotubes with a well-defined tube-to-tube spacing (spaced tubes) and single-wall morphology. By optimizing the anodization conditions (electrolyte, temperature, etc.), the growth rate of spaced tubes can be ≈25 times faster than in conventional approaches while maintaining a tube-to-tube spacing of ≈100 nm. We show that the origin of the tube-to-tube spacing is self-ordering of nanotubes on two different scales – the primary large tubes are embedded in a matrix of secondary, very short nanotubes with a small diameter. Preferential etching of the small tubes during anodic growth leaves behind an ordered array of spaced individual tubes with a well-defined tube-to-tube spacing. Keywords: Anodization, TiO2 nanotubes, Two-size scale, Fast-growth, DMSO

One prominent cause of implant failure is infection; therefore, research is focusing on developing surface coatings that render the surface resistant to colonization by micro-organisms. Permanently attached coatings of antimicrobial molecules are of particular interest because of the reduced cytoxicity and lower risk of developing resistance compared to controlled release coatings. In this study, we focus on the chemical grafting of bioactive molecules on titanium. To concentrate the molecules at the metallic implant surface, we propose electrophoretic deposition (EPD) applying alternating current (AC) signals with an asymmetrical wave shape. We show that for the model molecule bovine serum albumin (BSA), as well as for the clinically relevant antifungal lipopeptide caspofungin (CASP), the deposition yield is drastically improved by superimposing a DC offset in the direction of the high-amplitude peak of the AC signal. Additionally, in order to produce immobilized CASP coatings, this experimental AC/DC-EPD method is combined with an established surface activation protocol. Principle component analysis (PCA) of time-of-flight secondary ion mass spectrometry (ToF-SIMS) data confirm the immobilization of CASP with higher yield as compared to a diffusion-controlled process, and higher purity than the clinical CASP starting suspensions. Scratch testing data indicate good coating adhesion. Importantly, the coatings remain active against the fungal pathogen C. albicans as shown by in vitro biofilm experiments. In summary, this paper delivers a proof-of-concept for the application of AC-EPD as a fast grafting tool for antimicrobial molecules without compromising their activities.

In the present work we show how to achieve different nanotube morphologies (namely, not only single- and double-walled tubes, but also a tube-in-tube configuration) by combining specific anodization parameters. We characterize as-grown tube layers in terms of morphology, chemical composition and properties. As-grown tubes exhibit a double-walled morphology, that is, they consist of an inner and an outer shell. The low quality inner shell can be removed by an optimized chemical treatment thus leading to nanotubes of a higher quality oxide and with a single-walled nature. Double-walled tubes grown at low electrolyte temperature provide a thick inner shell that after adequate annealing can form a unique tube-in-tube morphology.

We report on free-standing Ta3N5 nanotubular membranes with open top and bottom, used as visible-light-active, flow-through photocatalytic micro-reactors. We grow first a robust anodic Ta2O5 layer, lift-off a membrane and convert to Ta3N5. Such membranes can easily, in a flow-through mode, degrade methylene blue under visible light (wavelength >400 nm) or solar illumination.

Herein we investigate the efficiency of various biomimetic coatings for localized drug delivery, using vancomycin as key therapeutic drug, which is a widely used antibiotic for the treatment of strong infections caused by positive Gram bacteria. We evaluate classical hydroxyapatite and biomimetic hydroxyapatite-collagen coatings obtained by electrochemical deposition as well as TiO2 nanotubes arrays obtained by electrochemical anodization. Surface morphology, compositional and structural data confirm the incorporation of vancomycin into the layers and drug release profiles for vancomycin evaluate their release ability. Namely, hydroxyapatite coatings lead to a ≈92% vancomycin release after 30h and hydroxyapatite-collagen to 85%, while the TiO2 nanotubes layers lead to 78% release. The antibacterial effect of such drug loaded coatings is evaluated against S. aureus (Gram-positive bacteria). Our study shows that the vancomycin incorporated hydroxyapatite coatings lead to a faster release, while the nanotubular coatings may lead to longer time release and additionally both types of coatings ensure a good antibacterial inhibition.

Solar driven photoelectrochemical water splitting (PEC-WS) using semiconductor photoelectrodes represents a promising approach for a sustainable and environmentally friendly production of renewable energy vectors and fuel sources, such as dihydrogen (H2). In this context, titanium dioxide (TiO$_2$) and iron oxide (hematite, $\alpha$-Fe$_2$O$_3$) are among the most investigated candidates as photoanode materials, mainly owing to their resistance to photocorrosion, non-toxicity, natural abundance, and low production cost. Major drawbacks are, however, an inherently low electrical conductivity and a limited hole diffusion length that significantly affect the performance of TiO$_2$ and $\alpha$-Fe$_2$O$_3$ in PEC devices. To this regard, one-dimensional (1D) nanostructuring is typically applied as it provides several superior features such as a significant enlargement of the material surface area, extended contact between the semiconductor and the electrolyte and, most remarkably, preferential electrical transport that overall suppress charge carrier recombination and improve TiO$_2$ and $\alpha$-Fe$_2$O$_3$ photo-electrocatalytic properties. The present review describes various synthetic methods, properties and PEC applications of 1D-photoanodes (nanotubes, nanorods, nanofibers, nanowires) based on titania, hematite, and on $\alpha$-Fe$_2$O$_3$/TiO$_2$ heterostructures. Various routes towards modification and enhancement of PEC activity of 1D photoanodes are also discussed including doping, decoration with co-catalysts and heterojunction engineering. Finally, the challenges related to the optimization of charge transfer kinetics in both oxides are highlighted.

TiO 2 nanotube (TNT) arrays directly grown on a transparent conductive support such as e.g. a layer of fluorine doped tin oxide (FTO) are highly desirable for solar energy application including dye-sensitized solar cells (DSSC) and photoelectrochemical water splitting (PEC-WS). In this paper we report on the fabrication of fully transparent TNT arrays formed by complete self-organizing electrochemical anodization of metallic Ti thin layers deposited on the FTO glass substrate by using electron beam evaporation and/or magnetron sputtering. It is clearly shown for the first time that the quality of the deposited titanium film (e.g. amount and size of pinholes) governs its adherence to the substrate and subsequently the anodization process itself. Mechanical properties of the deposited Ti films were investigated by tribology experiments. The main difference between the sputtered and evaporated titanium layers are the lower film density and considerably higher amount of pinholes of the latter. The grown TNT films were further characterized by SEM, X-ray diffraction, and UV–Vis spectroscopy. The sputtered layers overperformed the evaporated layers by 20% when applied for DSSC. An even greater difference was observed in the case of aqueous electrolyte based PEC-WS, where the sputtered layers showed five times higher activity.

Single-atom (SA) catalysis is a novel frontline in the catalysis field due to the often drastically enhanced specific activity and selectivity of many catalytic reactions. Here, an atomic-scale defect engineering approach to form and control traps for platinum SA sites as co-catalyst for photocatalytic H

With a large-scale usage of portable electric appliances, a high demand for increasingly high density energy storage devices has emerged. MoO3 has, in principle, a large potential as negative electrode material in supercapacitive devices, due to high charge densities that can be obtained from its reversible redox reactions. Nevertheless, the extremely poor electrochemical stability of MoO3 in aqueous electrolytes prevents a practical use in high capacitance devices. In this work, we describe how to overcome this severe stability issue by forming amorphous molybdenum oxide/tantalum oxide nanotubes by anodic oxidation of a Mo-Ta alloy. The presence of a critical amount of Ta-oxide (> 20 at-%) prevents the electrochemical decay of the MoO3 phase and thus yields an extremely high stability. Due to the protection provided by tantalum oxide, no capacitance losses are measureable after 10000 charg-ing/discharging cycles.

Pt nanoparticles are typically decorated as co‐catalyst on semiconductors to enhance the photocatalytic performance. Due to the low abundance and high cost of Pt, reaching a high activity with minimized co‐catalyst loadings is a key challenge in the field. We explore a dewetting‐dealloying strategy to fabricate on TiO2 nanotubes nanoporous Pt nanoparticles, aiming at improving the co‐catalyst mass activity for H2 generation. For this, we sputter first Pt‐Ni bi‐layers of controllable thickness (nm range) on highly ordered TiO2 nanotube arrays, and then induce dewetting‐alloying of the Pt‐Ni bi‐layers by a suitable annealing step in a reducing atmosphere: the thermal treatment causes the Pt and Ni films to agglomerate and at the same time mix with each other, forming on the TiO2 nanotube surface metal islands of a mixed PtNi composition. In a subsequent step we perform chemical dealloying of Ni that is selectively etched out from the bimetallic dewetted islands, leaving behind nanoporous Pt decorations. Under optimized conditions, the nanoporous Pt‐decorated TiO2 structures show a>6 times higher photocatalytic H2 generation activity compared to structures modified with a comparable loading of dewetted, non‐porous Pt. We ascribe this beneficial effect to the nanoporous nature of the dealloyed Pt co‐catalyst, which provides an increased surface‐to‐volume ratio and thus a more efficient electron transfer and a higher density of active sites at the co‐catalyst surface for H2 evolution., Combined dewetting‐alloying and dealloying of metal thin films provides reliable nanostructuring tools to form on TiO2 nanotubes a nanoporous Pt co‐catalyst that exhibits a significantly enhanced mass activity for photocatalytic H2 evolution.

Photoelectrochemical (PEC) water splitting is a promising method for the conversion of solar energy into chemical energy stored in the form of hydrogen. Nanostructured hematite (α‐Fe2O3) is one of the most attractive materials for a highly efficient charge carrier generation and collection due to its large specific surface area and the short minority carrier diffusion length. In the present work, the PEC water splitting performance of nanostructured α‐Fe2O3 is investigated which was prepared by anodization followed by annealing in a low oxygen ambient (0.03 % O2 in Ar). It was found that low oxygen annealing can activate a significant PEC response of α‐Fe2O3 even at a low temperature of 400 °C and provide an excellent PEC performance compared with classic air annealing. The photocurrent of the α‐Fe2O3 annealed in the low oxygen at 1.5 V vs. RHE results as 0.5 mA cm−2, being 20 times higher than that of annealing in air. The obtained results show that the α‐Fe2O3 annealed in low oxygen contains beneficial defects and promotes the transport of holes; it can be attributed to the improvement of conductivity due to the introduction of suitable oxygen vacancies in the α‐Fe2O3. Additionally, we demonstrate the photocurrent of α‐Fe2O3 annealed in low oxygen ambient can be further enhanced by Zn‐Co LDH, which is a co‐catalyst of oxygen evolution reaction. This indicates low oxygen annealing generates a promising method to obtain an excellent PEC water splitting performance from α‐Fe2O3 photoanodes., Low oxygen annealing can activate a significant photoelectrochemical response of α‐Fe2O3 even at a low temperature of 400 °C and provide an excellent PEC performance compared with classic air annealing. The α‐Fe2O3 annealed in low oxygen ambient contains beneficial defects and promotes the transport of photogenerated holes; it can be attributed to the introduction of suitable oxygen vacancies in the α‐Fe2O3.

Titanium dioxide (TiO2) nanotube coated substrates have revolutionized the concept of implant in a number of ways, being endowed with superior osseointegration properties and local drug delivery capacity. While accumulating reports describe the influence of nanotube diameter on cell behavior, little is known about the effects of nanotube lateral spacing on cells involved in bone regeneration. In this context, in the present study the MC3T3-E1 murine pre-osteoblast cells behavior has been investigated by using TiO2 nanotubes of ~78 nm diameter and lateral spacing of 18 nm and 80 nm, respectively. Both nanostructured surfaces supported cell viability and proliferation in approximately equal extent. However, obvious differences in the cell spreading areas, morphologies, the organization of the actin cytoskeleton and the pattern of the focal adhesions were noticed. Furthermore, investigation of the pre-osteoblast differentiation potential indicated a higher capacity of larger spacing nanostructure to enhance the expression of the alkaline phosphatase, osteopontin and osteocalcin osteoblast specific markers inducing osteogenic differentiation. These findings provide the proof that lateral spacing of the TiO2 nanotube coated titanium (Ti) surfaces has to be considered in designing bone implants with improved biological performance.

Here we report that both-end open anodic TiO

Hollow titanium dioxide (TiO2) nanotubes offer substantially higher drug loading capacity and slower drug release kinetics compared to solid drug nanocarriers of comparable size. In this report, we load TiO2 nanotubes with iron oxide nanoparticles to facilitate site-specific magnetic guidance and drug delivery. We generate magnetic TiO2 nanotubes (TiO2NTs) by incorporating a ferrofluid containing Ø ≈ 10 nm iron oxide nanoparticles in planar sheets of weakly connected TiO2 nanotubes. After thermal annealing, the magnetic tubular arrays are loaded with therapeutic drugs and then sonicated to separate the nanotubes. We demonstrate that magnetic TiO2NTs are non-toxic for HeLa cells at therapeutic concentrations (≤200 µg/mL). Adhesion and endocytosis of magnetic nanotubes to a layer of HeLa cells are increased in the presence of a magnetic gradient field. As a proof-of-concept, we load the nanotubes with the topoisomerase inhibitor camptothecin and achieve a 90% killing efficiency. We also load the nanotubes with oligonucleotides for cell transfection and achieve 100% cellular uptake efficiency. Our results demonstrate the potential of magnetic TiO2NTs for a wide range of biomedical applications, including site-specific delivery of therapeutic drugs.

TiO

Anatase and rutile mixed-phase TiO2 with an ideal ratio has been proven to significantly enhance photoelectrochemical (PEC) activity in water-splitting applications due to suppressing the electron&ndash, hole recombination. However, the mechanism of this improvement has not been satisfactory described yet. The PEC water oxidation (oxygen evolution) at the interface of TiO2 photoanode and electrolyte solution is determined by the fraction of the photogenerated holes that reach the solution and it is defined as the hole transfer efficiency. The surface and bulk recombination processes in semiconductor photoanodes majorly influence the hole transfer efficiency. In this work, we study the hole transfer process involved in mixed-phase TiO2 nanotube arrays/solution junction using intensity-modulated photocurrent and photovoltage spectroscopy (IMPS and IMVS), then, we correlate the obtained hole transfer rate constants to (photo)electrochemical impedance spectroscopy (PEIS) measurements. The results suggest that the enhanced performance of the TiO2 mixed-phase is due to the improved hole transfer rate across the TiO2/liquid interface as well as to the decrease in the surface trap recombination of the holes.

Illumination of anatase in an aqueous methanolic solution leads to the formation of Ti