SearcharxivSearch

arXiv subjects

Xuemei Zhou

Publications and source records attributed to Xuemei Zhou.

At least 19 recordsLinked to original sources

PointPCA+: Extending PointPCA objective quality assessment metric

A computationally-simplified and descriptor-richer Point Cloud Quality Assessment (PCQA) metric, namely PointPCA+, is proposed in this paper, which is an extension of PointPCA. PointPCA proposed a set of perceptually-relevant descriptors based on PCA decomposition that were applied to both the geometry and texture data of point clouds for full reference PCQA. PointPCA+ employs PCA only on the geometry data while enriching existing geometry and texture descriptors, that are computed more efficiently. Similarly to PointPCA, a total quality score is obtained through a learning-based fusion of individual predictions from geometry and texture descriptors that capture local shape and appearance properties, respectively. Before feature fusion, a feature selection module is introduced to choose the most effective features from a proposed super-set. Experimental results show that PointPCA+ achieves high predictive performance against subjective ground truth scores obtained from publicly available datasets. The code is available at \url{https://github.com/cwi-dis/pointpca_suite/}.

cs.CV

PointPCA: Point Cloud Objective Quality Assessment Using PCA-Based Descriptors

Point clouds denote a prominent solution for the representation of 3D photo-realistic content in immersive applications. Similarly to other imaging modalities, quality predictions for point cloud contents are vital for a wide range of applications, enabling trade-off optimizations between data quality and data size in every processing step from acquisition to rendering. In this work, we focus on use cases that consider human end-users consuming point cloud contents and, hence, we concentrate on visual quality metrics. In particular, we propose a set of perceptually relevant descriptors based on Principal Component Analysis (PCA) decomposition, which is applied to both geometry and texture data for full-reference point cloud quality assessment. Statistical features are derived from these descriptors to characterize local shape and appearance properties for both a reference and a distorted point cloud. The extracted statistical features are subsequently compared to provide corresponding predictions of visual quality for the distorted point cloud. As part of our method, a learning-based approach is proposed to fuse these individual predictors to a unified perceptual score. We validate the accuracy of the individual predictors, as well as the unified quality scores obtained after regression against subjectively annotated datasets, showing that our metric outperforms state-of-the-art solutions. Insights regarding design decisions are provided through exploratory studies, evaluating the performance of our metric under different parameter configurations, attribute domains, color spaces, and regression models. A software implementation of the proposed metric is made available at the following link: https://github.com/cwi-dis/pointpca.

cs.MM

Noble-Metal-Free Photocatalytic Hydrogen Evolution Activity: The Impact of Ball Milling Anatase Nanopowders with TiH2

In this work, we demonstrate that a well-established and facile ball milling approach using mixtures of commercial anatase nanoparticles and TiH2 introduces noble-metal-free photocatalytic H2 activity to titania. We characterize this synergistic effect in view of the nature of defects, state of hydroxylation, and investigate the effect on the energetics and kinetics of electronic states and the resulting H2 evolution performance.

physics.chem-ph

Black Magic in Gray Titania: Noble-Metal-Free Photocatalytic H2 Evolution from Hydrogenated Anatase

"Black" TiO2 has gained increasing interest because of its outstanding properties and promising applications in a wide range of fields. Among the outstanding features of the material is that certain synthesis processes lead to the formation of an intrinsic co-catalytic center and thus enable noble-metal free photocatalytic H2 generation. In this work, we report "grey TiO2" by an appropriate hydrogenation treatment exhibits excellent photocatalytic hydrogen. In this case, by the employment of thermally stable and high-surface-area TiO2 nanoparticles as well as mesoporous particles as the hydrogenation precursor, the appropriate extent of reduction of TiO2 (coloration) and the formation of Ti3+ is the key for the efficient noble-metal-free photocatalytic H2 generation. The EPR results reveal that "grey TiO2" shows stronger Ti3+ feature at g ca. 1.93 than "black TiO2" contributing to the intrinsic catalytic center for H2 evolution.

physics.chem-ph

Intrinsically Activated SrTiO3: Photocatalytic H2 Evolution from Neutral Aqueous Methanol Solution in the Absence of Any Noble Metal Cocatalyst

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).

cond-mat.mtrl-sci

Magneli-Phases in Anatase Strongly Promote Co-Catalyst-Free Photocatalytic Hydrogen Evolution

Magneli phases of titanium dioxide (such as Ti4O7, Ti5O9, etc.) provide electronic properties, namely a stable metallic behavior at room temperature. In this manuscript, we demonstrate that nanoscopic Magneli phases, formed intrinsically in anatase during a thermal aerosol synthesis, can enable significant photocatalytic H2 generation. This without the use of any extrinsic co-catalyst in anatase. Under optimized conditions, mixed phase particles of 30 percent anatase, 25 percent Ti4O7 and 20 percent Ti5O9 are obtained that can provide, under solar light, direct photocatalytic H2 evolution at a rate of 145 micromol h-1 g-1. These anatase particles contain 5-10 nm size inter-grown phases of Ti4O7 and Ti5O9. Key is the metallic band of Ti4O7 that induces a particle internal charge separation and transfer cascade with suitable energetics and favorable dimensions that are highly effective for H2 generation.

cond-mat.mtrl-sci

Spaced TiO$_2$ Nanotube Arrays Allow for High Performance Hierarchical Supercapacitor Structure

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.

physics.chem-ph

Black and White Anatase, Rutile and Mixed Forms: Band-Edges and Photocatalytic Activity

Here we investigate the band-level energetics of "black" hydrogenated titania in different polymorphs using in-situ photoelectrochemical measurements and XPS valence band measurements. We find that the conduction band of black rutile is higher in energy than in black anatase by 0.4 eV. For photocatalytic hydrogen generation, in a polymorph hetero-junction such as in black Degussa P25, thus black rutile can act as a photosensitizer while black anatase provides charge-mediation catalysis onto H2O to generate H2. By optimizing the thermal reduction conditions of black anatase/rutile junctions the H2 production can be significantly increased.

physics.chem-ph

Nanoporous AuPt and AuPtAg alloy co-catalysts formed by dewetting-dealloying on ordered TiO2 nanotube surface lead to significantly enhanced photocatalytic H2 generation

Effective co-catalysts are of key importance for photocatalytic H2 generation from aqueous environments. An attractive co-catalyst candidate are AuPt (metastable) alloys due to the synergistic electronic and chemical interaction of the constituents in the charge transfer and H2 evolution process. Here we introduce the fabrication of AuPt alloy nanoparticles with nanoporosity (pore size of 2-5 nm) fabricated on spaced TiO2 nanotubes. By dewetting a layered AgAuPt coating, we form AuPtAg alloy nanoparticles. From these alloys, Ag can selectively be dissolved leading to the desired nanoporous AuPt alloy particles with diameter in the range of 10-70 nm deposited as a gradient on the TiO2 nanotubes. A significant enhancement of photocatalytic H2 generation is obtained compared to the same loading of monometallic or nonporous alloy. The nanoporous AuPt particles provide not only a large surface area to volume ratio (and are thus more effective) but also show the intrinsic synergy of a AuPt alloy for H2 generation.

physics.app-ph

Photocatalysis with TiO2 Nanotubes: Colorful Reactivity and Designing Site-Specific Photocatalytic Centers into TiO2 Nanotubes

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.

physics.app-ph

Black TiO2 nanotubes formed by high energy proton implantation show noble-metal-co-catalyst free photocatalytic H2-evolution

We apply high-energy proton ion-implantation to modify TiO2 nanotubes selectively at their tops. In the proton-implanted region we observe the creation of intrinsic co-catalytic centers for photocatalytic H2-evolution. We find proton implantation to induce specific defects and a characteristic modification of the electronic properties not only in nanotubes but also on anatase single crystal (001) surfaces. Nevertheless, for TiO2 nanotubes a strong synergetic effect between implanted region (catalyst) and implant-free tube segment (absorber) can be obtained.

physics.chem-ph

Stable Co-Catalyst-Free Photocatalytic H2 Evolution From Oxidized Titanium Nitride Nanopowders

In the present work, a simple strategy is used to thermally oxidize TiN nanopowder (ca. 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 photocatalytic activity for hydrogen evolution under AM1.5 conditions - this 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.

cond-mat.mtrl-sci

Visible Light Triggered Drug Release from TiO2 Nanotube Arrays: A Novel Controllable Antibacterial Platform

In this work, we use a double-layered stack of TiO2 nanotubes (TiNTs) to construct a visible-light triggered drug delivery system. 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 the principle, we loaded antibiotic (ampicillin sodium (AMP)) in the lower part of the TiO2 nanotube stack, triggered visible light induced release, and carried out antibacterial studies. The release from the platform becomes most controllable if the drug is silane-grafted in hydrophilic bottom layer for drug storage. Thus visible-light photocatalysis can also determine the release kinetics of the active drug from the nanotube wall.

physics.chem-ph

TiO2 nanotubes: N-ion implantation at low-dose provides noble-metal-free photocatalytic H2-evolution activity

Low-dose nitrogen implantation induces in TiO2 nanotubes a co-catalytic activity for photocatalytic H2-evolution. The use of an ion implantation process leads to a N-implanted zone only at the top part of the tubes. The coupling of this top layer and the underlying non-implanted part of the nanotubes strongly contributes to an efficient carrier separation and thus to a significantly enhanced H2 generation.

physics.chem-ph

Self-ordered Mo-oxide Nanotube Arrays as Precursor for Aligned MoOx/MoS2 Core-Shell Nanotubular Structures with a High Density of Reactive Sites

In the present work we demonstrate the self-organized formation of anodic Mo-oxide nanotube arrays grown on a Mo sheet under suitable electrochemical conditions in glycerol/NH4F electrolytes. The resulting amorphous tubes can be crystallized by annealing to MoO2 or MoO3. The tube walls then can be further sulfurized fully or partially to Mo-sulfide to form well-ordered arrays of vertically aligned MoOx/MoS2 nanotubes. Under optimized conditions, defined MoS2 sheets form on the oxide walls in a layer by layer low angle zig-zag arrangement that provide a high density of reactive stacking faults. These core-shell nanotube arrays, consisting of tubes with a conductive suboxide core and a functional high defect density MoS2 coating, are highly promising for applications such as electrocatalysis (hydrogen evolution) or ion insertion devices.

cond-mat.mtrl-sci

Graphitic C3N4 Sensitized TiO2 Nanotube Layers: A Visible Light Activated Efficient Antimicrobial Platform

In this work, we introduce a facile procedure to graft a thin graphitic C3N4 (g-C3N4) layer on aligned TiO2 nanotube arrays (TiNT) by one-step chemical vapor deposition (CVD) approach. This provides a platform to enhance the visible-light response of TiO2 nanotubes for antimicrobial applications. The formed g- C3N4/TiNT binary nanocomposite exhibits excellent bactericidal efficiency against E. coli as a visiblelight activated antibacterial coating.

physics.bio-ph

Carbon Decorated TiO2 Nanotube Membranes: A Renewable Nanofilter for Size- and Charge Selective Enrichment of Proteins

In this work, we design a TiO2 nanomembrane (TiNM) that can be used as a nanofilter platform for a selective enrichment of specific proteins. After use the photocatalytic properties of TiO2 allow to decompose unwanted remnant on the substrate and thus make the platform reusable. To construct this platform we fabricate a free-standing TiO2 nanotube array and remove the bottom oxide to form a both-end open TiNM. By pyrolysis of the natural tube wall contamination (C/TiNM), the walls become decorated with graphitic carbon patches. Owing to the large surface area, the amphiphilic nature and the charge adjustable character, this C/TiNM can be used to extract and enrich hydrophobic and charged biomolecules from solutions. Using human serum albumin (HSA) as a model protein as well as protein mixtures, we show that the composite membrane exhibits a highly enhanced loading capacity and protein selectivity and is reusable after a short UV treatment.

cond-mat.mtrl-sci

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