2.3. Evaluation of Photocatalytic Water Splitting 6507 2.3.1. Photocatalytic Activity 6507 2.3.2. Photocatalytic Stability 6507 3. UV-Active Photocatalysts for Water Splitting 6507 3.1. d0 Metal Oxide Photocatalyts 6507 3.1.1. Ti-, Zr-Based Oxides 6507 3.1.2. Nb-, Ta-Based Oxides 6514 3.1.3. W-, Mo-Based Oxides 6517 3.1.4. Other d0 Metal Oxides 6518 3.2. d10 Metal Oxide Photocatalyts 6518 3.3. f0 Metal Oxide Photocatalysts 6518 3.4. Nonoxide Photocatalysts 6518 4. Approaches to Modifying the Electronic Band Structure for Visible-Light Harvesting 6519

Semiconductor-based Photocatalytic Hydrogen Generation

Graphene’s success has shown that it is possible to create stable, single and few-atom-thick layers of van der Waals materials, and also that these materials can exhibit fascinating and technologically useful properties. Here we review the state-of-the-art of 2D materials beyond graphene. Initially, we will outline the different chemical classes of 2D materials and discuss the various strategies to prepare single-layer, few-layer, and multilayer assembly materials in solution, on substrates, and on the wafer scale. Additionally, we present an experimental guide for identifying and characterizing single-layer-thick materials, as well as outlining emerging techniques that yield both local and global information. We describe the differences that occur in the electronic structure between the bulk and the single layer and discuss various methods of tuning their electronic properties by manipulating the surface. Finally, we highlight the properties and advantages of single-, few-, and many-layer 2D materials in...

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Progress, Challenges, and Opportunities in Two-Dimensional Materials Beyond Graphene

Graphene-Like Two-Dimensional Materials

UV-Visible ار راد ن .د TiO2 ( تیفرظ راون مان هب نورتکلا یاراد یژرنا زارت لماش VB و ) رگید زارت ی یژرنا اب ( ییاناسر راون مان هب نورتکلا زا یلاخ و رتلااب VB یم ) .دشاب ت ود نیا نیب یژرنا توافت یژرنا فاکش زار ، پگ دناب هدیمان یم .دوش هک ینامز زا نورتکلا لاقتنا VB هب VB یم ماجنا دریگ ، TiO2 اب ودح یژرنا بذج د ev 2 / 3 ، نورتکلا تفج کی دیلوت یم هرفح .دیامن و نورتکلا هرفح ی نا اب هدش دیلوت یم کرتشم حطس هب لاقت ثعاب دناوت شنکاو ماجنا اه یی ددرگ . TiO2 دربراک ،دراد یدایز یاه هلمج زا یم ناوت اوه یگدولآ هیفصت یارب (CO2) و بآ و ... نآ زا هدافتسا درک .

Advanced Nanoarchitectures for Solar Photocatalytic Applications

Two-dimensional layered materials (2DLMs) have been a central focus of materials research since the discovery of graphene just over a decade ago. Each layer in 2DLMs consists of a covalently bonded, dangling-bond-free lattice and is weakly bound to neighbouring layers by van der Waals interactions. This makes it feasible to isolate, mix and match highly disparate atomic layers to create a wide range of van der Waals heterostructures (vdWHs) without the constraints of lattice matching and processing compatibility. Exploiting the novel properties in these vdWHs with diverse layering of metals, semiconductors or insulators, new designs of electronic devices emerge, including tunnelling transistors, barristors and flexible electronics, as well as optoelectronic devices, including photodetectors, photovoltaics and light-emitting devices with unprecedented characteristics or unique functionalities. We review the recent progress and challenges, and offer our perspective on the exploration of 2DLM-based vdWHs for future application in electronics and optoelectronics. With a dangling-bond-free surface, two dimensional layered materials (2DLMs) can enable the creation of diverse van der Waals heterostructures (vdWHs) without the conventional constraint of lattice matching or process compatibility. This Review discusses the recent advances in exploring 2DLM vdWHs for future electronics and optoelectronics.

Van der Waals heterostructures and devices

First-principles calculations are performed to study the electronic and magnetic properties of VX2 monolayers (X = S, Se). Our results unveil that VX2 monolayers exhibit exciting ferromagnetic behavior, offering evidence of the existence of magnetic behavior in pristine 2D monolayers. Furthermore, interestingly, both the magnetic moments and strength of magnetic coupling increase rapidly with increasing isotropic strain from −5% to 5% for VX2 monolayers. It is proposed that the strain-dependent magnetic moment is related to the strong ionic–covalent bonds, while both the ferromagnetism and the variation in strength of magnetic coupling with strain arise from the combined effects of both through-bond and through-space interactions. These findings suggest a new route to facilitate the design of nanoelectronic devices for complementing graphene.

Evidence of the existence of magnetism in pristine VX₂ monolayers (X = S, Se) and their strain-induced tunable magnetic properties.

Very recently, two-dimensional nanosheets of MoSe(2), MoTe(2) and WS(2) were successfully synthesized experimentally [Science, 2011, 331, 568]. In the present work, the electronic and magnetic properties of perfect, vacancy-doped, and nonmetal element (H, B, C, N, O, and F) adsorbed MoSe(2), MoTe(2) and WS(2) monolayers are systematically investigated by means of first-principles calculations to give a detailed understanding of these materials. It is found that: (1) MoSe(2), MoTe(2) and WS(2) exhibit surprising confinement-induced indirect-direct-gap crossover; (2) among all the neutral native vacancies of MoSe(2), MoTe(2) and WS(2) monolayers, only the Mo vacancy in MoSe(2) can induce spin-polarization and long-range antiferromagnetic coupling; (3) adsorption of nonmetal elements on the surface of MoSe(2), MoTe(2) and WS(2) nanosheets can induce a local magnetic moment; H-absorbed WS(2), MoSe(2), and MoTe(2) monolayers and F-adsorbed WS(2) and MoSe(2) monolayers show long-range antiferromagnetic coupling between local moments even when their distance is as long as ∼12 A. These findings are a useful addition to the experimental studies of these new synthesized two-dimensional nanosheets, and suggest a new route to facilitate the design of spintronic devices for complementing graphene. Further experimental studies are expected to confirm the attractive predictions.

Electronic and magnetic properties of perfect, vacancy-doped, and nonmetal adsorbed MoSe2, MoTe2 and WS2 monolayers

Cu2O microcrystals with well-formed facets were synthesized by a simple hydrothermal method. The surface stabilities and photocatalytic properties of Cu2O microcrystals were systematically investigated. Cu2O {100} and {110} facets gradually disappear and transform into nanosheets during the photodegradation of methyl orange (MO) dye. With the increase of irradiation time, Cu2O microcrystals completely transform into nanosheets with {111} facets. The finally formed nanosheets exhibit stable photocatalytic activities. On the basis of both experimental analysis and theoretical calculations, a novel model of charge separation among crystal faces was proposed and the morphology transformation mechanism accompanied by MO bleaching was discussed. It is concluded that Cu2O exposing {111} facets can be used as a stable photocatalyst.

Crystal Faces of Cu2O and Their Stabilities in Photocatalytic Reactions

The geometric and electronic structures of graphene adsorption on MoS2 monolayer have been studied by using density functional theory. It is found that graphene is bound to MoS2 with an interlayer spacing of 3.32 A and with a binding energy of −23 meV per C atom irrespective of adsorption arrangement, indicating a weak interaction between graphene and MoS2. A detailed analysis of the electronic structure indicates that the nearly linear band dispersion relation of graphene can be preserved in MoS2/graphene hybrid accompanied by a small band-gap (2 meV) opening due to the variation of on-site energy induced by MoS2. These findings are useful complement to experimental studies of this new synthesize system and suggest a new route to facilitate the design of devices where both finite band-gap and high carrier mobility are needed.

Graphene adhesion on MoS₂ monolayer: an ab initio study.

Here we present first-principles calculations to investigate systematically the electronic behavior and the electron energy low-loss spectra (EELS) of monolayer, bilayer, four-layer, and bulk configurations of periodic GaX (X = S, Se), as well as the effect of mechanical strain on the electronic properties of the GaX monolayer. We predicate that the GaX monolayer is a semiconductor with an indirect band gap, however, the difference between the direct and indirect gaps is so small that electrons can transfer easily between this minimum with a small amount of thermal energy. Owning to strong surface effects, the electronic and dielectric properties of GaX vary drastically with number of layers in a sheet. In detail, the band gap increases from multilayer-to-single layer and EELS shifts towards larger wavelengths with a decrease in the layer thickness. Moreover, we demonstrate that the band gaps of GaX monolayers can be widely tuned by mechanical deformation, making them potential candidates for tunable nanodevices. The present study provides theoretical insight leading to a better understanding of these novel 2D structures.

Meng Guo

Papers

Evidence of the existence of magnetism in pristine VX₂ monolayers (X = S, Se) and their strain-induced tunable magnetic properties.

Electronic and magnetic properties of perfect, vacancy-doped, and nonmetal adsorbed MoSe2, MoTe2 and WS2 monolayers

Crystal Faces of Cu2O and Their Stabilities in Photocatalytic Reactions

Graphene adhesion on MoS₂ monolayer: an ab initio study.

Tunable electronic and dielectric behavior of GaS and GaSe monolayers