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When using single atoms (SAs) as a co‐catalyst in photocatalytic H2 generation, achieving a well‐dispersed, evenly distributed and adjustable SA surface density on a semiconductor surface is a challenging task. In the present work we use the planar adsorption of tetrakis‐(4‐carboxyphenyl)‐porphyrin (TCPP) and its platinum coordinated analogue, Pt‐TCPP, onto anatase TiO2 surfaces to establish a spatially controlled decoration of SAs. We show that the surface Pt SA density can be very well controlled by co‐adsorption of Pt‐TCPP and TCPP in the planar monolayer regime, and by adjusting the Pt‐TCPP to TCPP ratio a desired well dispersed surface density of SAs up to 2.6×105 atoms μm−2 can be established (which is the most effective Pt SA loading for photocatalysis). This distribution and the SA state are maintained after a thermal treatment in air, and an optimized SA density as well as a most active form of Pt for photocatalytic H2 evolution can be established and maintained. [ABSTRACT FROM AUTHOR]

In this report, a 2D MOF nanosheet derived Pd single‐atom catalyst, denoted as Pd‐MOF, was fabricated and examined for visible light photocatalytic hydrogen evolution reaction (HER). This Pd‐MOF can provide a remarkable photocatalytic activity (a H2 production rate of 21.3 mmol/gh in the visible range), which outperforms recently reported Pt‐MOFs (with a H2 production rate of 6.6 mmol/gh) with a similar noble metal loading. Notably, this high efficiency of Pd‐MOF is not due to different chemical environment of the metal center, nor by changes in the spectral light absorption. The higher performance of the Pd‐MOF in comparison to the analogue Pt‐MOF is attributed to the longer lifetime of the photogenerated electron‐hole pairs and higher charge transfer efficiency. [ABSTRACT FROM AUTHOR]

The present work demonstrates the self-organized formation of anodic molybdenum oxide nanotube arrays. The amorphous tubes can be crystallized to MoO2 or MoO3 and be converted fully or partially into molybdenum sulfide. Vertically aligned MoO x/MoS2 nanotubes can be formed when, under optimized conditions, defined MoS2 sheets form in a layer by layer arrangement that provide a high density of reactive stacking misalignments (defects). These core-shell nanotube arrays consist of a conductive suboxide core and a functional high defect density MoS2 coating. Such structures are highly promising for applications in electrocatalysis (hydrogen evolution) or ion insertion devices. [ABSTRACT FROM AUTHOR]

Low-dose nitrogen implantation induces an ion and damage profile in TiO2 nanotubes that leads to 'co-catalytic' activity for photocatalytic H2-evolution (without the use of any noble metal). Ion implantation with adequate parameters creates this active zone limited to the top part of the tubes. The coupling of this top layer and the underlying non-implanted part of the nanotubes additionally contributes to an efficient carrier separation and thus to a significantly enhanced H2 generation. [ABSTRACT FROM AUTHOR]

In this work, we use a double-layered stack of TiO2 nanotubes (TiNTs) to construct a visible-light-triggered drug delivery system. The key for visible light drug release is a hydrophobic cap on the nanotubes containing Au nanoparticles (AuNPs). The AuNPs allow for a photocatalytic scission of the hydrophobic chain under visible light. To demonstrate this principle, we loaded ampicillin (AMP) into the lower part of the TiO2 nanotube stack, triggered visiblelight- induced release, and carried out antibacterial studies. The release from the platform becomes most controllable if the drug is silane-grafted in the hydrophilic bottom layer for drug storage. Thus, visible light photocatalysis can also determine the release kinetics of the active drug from the nanotube wall. [ABSTRACT FROM AUTHOR]

A simple strategy is used to thermally oxidize TiN nanopowder (∼20 nm) to an anatase phase of a TiO2:Ti3+:N compound. In contrast to the rutile phase of such a compound, this photocatalyst provides activity for hydrogen evolution under AM1.5 conditions, without the use of any noble metal co-catalyst. Moreover the photocatalyst is active and stable over extended periods of time (tested for 4 months). Importantly, to achieve successful conversion to the active anatase polymorph, sufficiently small starting particles of TiN are needed. The key factor for catalysis is the stabilization of the co-catalytically active Ti3+ species against oxidation by nitrogen present in the starting material. [ABSTRACT FROM AUTHOR]

Differently modified TiO2 nanotubes were used to achieve a drastic change in the selectivity of a photocatalytic reaction. For the photocatalytic oxidation of toluene, depending on the electronic properties of TiO2 (anatase, rutile, Rudoped), a strong change in the main reaction product (namely benzoic acid versus benzaldehyde) can be achieved, and certain undesired reaction pathways can be completely shut down. [ABSTRACT FROM AUTHOR]

Nearly 100 % filling of TiO2 nanotubes with metals, including Ag, Cu, Au, and Pt, was achieved by defect‐sealing treatment at the bottom of the nanotubes, followed by metal deposition using nuclei formation/coalescence. The resulting short‐circuit‐free interdigitated electrode configurations can, for example, be used to fabricate memristive electrodes. [ABSTRACT FROM AUTHOR]

Peas in a pod: A highly aligned Aunp@TiO2 photocatalyst was formed by self‐organizing anodization of a Ti substrate followed by dewetting of a gold thin film. This leads to exactly one Au nanoparticle (np) per TiO2 nanocavity. Such arrays are highly efficient photocatalysts for hydrogen generation from ethanol. [ABSTRACT FROM AUTHOR]

When using single atoms (SAs) as a co‐catalyst in photocatalytic H2 generation, achieving a well‐dispersed, evenly distributed and adjustable SA surface density on a semiconductor surface is a challenging task. In the present work we use the planar adsorption of tetrakis‐(4‐carboxyphenyl)‐porphyrin (TCPP) and its platinum coordinated analogue, Pt‐TCPP, onto anatase TiO2 surfaces to establish a spatially controlled decoration of SAs. We show that the surface Pt SA density can be very well controlled by co‐adsorption of Pt‐TCPP and TCPP in the planar monolayer regime, and by adjusting the Pt‐TCPP to TCPP ratio a desired well dispersed surface density of SAs up to 2.6×105 atoms μm−2 can be established (which is the most effective Pt SA loading for photocatalysis). This distribution and the SA state are maintained after a thermal treatment in air, and an optimized SA density as well as a most active form of Pt for photocatalytic H2 evolution can be established and maintained. [ABSTRACT FROM AUTHOR]