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Ying Dai

Bio: Ying Dai is an academic researcher from Shandong University. The author has contributed to research in topics: Photocatalysis & Band gap. The author has an hindex of 87, co-authored 706 publications receiving 31538 citations. Previous affiliations of Ying Dai include North Carolina State University & Northern Illinois University.


Papers
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TL;DR: It is shown that such a photocatalyst can be obtained from silver chloride by exploiting its photosensitivity, and the resulting plasmonic photoc atalyst is highly efficient and stable under visible-light illumination.
Abstract: Nanoparticles (NPs) of noble metals can strongly absorb visible light because of their plasmon resonance, which is greatly influenced by their morphology and size. The phenomenon of plasmon resonance gives rise to important applications such as colorimetric sensors, photovoltaic devices, photochromic devices, and photocatalysts. Noble metal NPs exhibit characteristic optical and physical properties that are substantially different from those of the corresponding bulk materials. In particular, silver NPs show efficient plasmon resonance in the visible region, which Awazu et al. recently utilized to develop a plasmonic photocatalyst. In their study, TiO2 was deposited on NPs consisting of a silver core covered with a silica (SiO2) shell to prevent oxidation of Ag by direct contact with TiO2. Under UV illumination, this plasmonic photocatalyst exhibits enhanced catalytic activity, which increases with decreasing thickness of the SiO2 shell. To enhance the activity of a plasmonic photocatalyst, it is desirable to deposit silver NPs directly onto the surface of an active dielectric substrate without a protective shell, because the near-field effect of the NPs will be more strongly felt by the substrate. Herein we show that such a photocatalyst can be obtained from silver chloride by exploiting its photosensitivity, and the resulting plasmonic photocatalyst is highly efficient and stable under visible-light illumination. Silver halides are photosensitive materials extensively used as source materials in photographic films. On absorbing a photon, a silver halide particle generates an electron and a hole, and subsequently the photogenerated electron combines with an Ag ion to form an Ag atom. Ultimately, a cluster of silver atoms is formed within a silver halide particle upon repeated absorption of photons. Due to this instability under sunlight, which provides the very basis for chemical photography, silver halides are seldom used as photocatalysts. Nevertheless, there have been reports that under UV/Vis illumination AgCl deposited on a conducting support photocatalyzes O2 production from water in the presence of a small excess of silver ions in solution, and that under UV illumination AgBr dispersed on a silica support photocatalyzes H2 production from CH3OH/H2O solution. [21] In their study on the AgBr/SiO2 photocatalyst, Kakuta et al. [21] observed that Ag species are formed on AgBr in the early stage of the reaction, and AgBr is not destroyed under successive UV illumination. As suggested by Kakuta et al., electron–hole separation may occur smoothly in the presence of Ag species, and the latter may catalyze H2 production from alcohol radicals formed by photo-induced holes. If so, silver NPs formed on silver halide particles might be expected to be a stable photocatalyst under visible-light illumination due to their plasmon resonance. This expectation led us to prepare a new photocatalyst active and stable under visible light, namely, AgCl particles with silver NPs formed on their surface, by first treating Ag2MoO4 with HCl to form AgCl powder and then reducing some Ag ions in the surface region of the AgCl particles to Ag species (for details, see the Experimental Section). For convenience, these are referred to as Ag@AgCl particles. The X-ray diffraction (XRD) pattern of the Ag@AgCl product clearly shows that the cubic phase of Ag with lattice constant a= 4.0861 A (JCPDS file: 65-2871) coexists with the cubic phase of AgCl with lattice constant a= 5.5491 A (JCPDS file: 31-1238; see Figure 1). Scanning electron microscopy (SEM) images of the Ag@AgCl product (Figure 2) reveal that silver NPs with diameters in the range of 20–150 nm are deposited on the surface of AgCl particles with diameters in the range of 0.2–1.3 mm. The UV/Vis diffuse-reflectance spectra of Ag@AgCl, AgCl, and N-doped TiO2 (used as reference photocatalyst) are compared in Figure 3. In contrast to AgCl and N-doped TiO2, Ag@AgCl has a strong adsorption in the visible region which is almost as strong as that in the UV region. This is attributed to the plasmon resonance of silver NPs deposited on AgCl particles. To evaluate the photooxidation capability of Ag@AgCl, we examined the decomposition of methylic orange (MO) dye in solution over the Ag@AgCl sample under visible-light irradiation as a function of time (Figure 4). For comparison, we also carried out decomposition of the MO dye in solution over the N-doped TiO2 reference photocatalyst under visible[*] P. Wang, Prof. Dr. B. Huang, X. Qin, Prof. X. Zhang, Dr. J. Wei State Key Lab of Crystal Materials Shandong University, Jinan 250100 (China) E-mail: bbhuang@sdu.edu.cn Homepage: http://www.icm.sdu.edu.cn/index.php

1,327 citations

Journal ArticleDOI
TL;DR: The ZnO with oxygen vacancies are found to be efficient for photodecomposition of 2,4-dichlorophenol under visible light irradiation and a narrowing bandgap can be confirmed by the enhancement of the photocurrent response when theZnO was irradiated with visible light.
Abstract: Oxygen vacancies in crystal have important impacts on the electronic properties of ZnO. With ZnO2 as precursors, we introduce a high concentration of oxygen vacancies into ZnO successfully. The obtained ZnO exhibits a yellow color, and the absorption edge shifts to longer wavelength. Raman and XPS spectra reveal that the concentration of oxygen vacancies in the ZnO decreased when the samples are annealed at higher temperature in air. It is consistent with the theory calculation. The increasing of oxygen vacancies results in a narrowing bandgap and increases the visible light absorption of the ZnO. The narrowing bandgap can be confirmed by the enhancement of the photocurrent response when the ZnO was irradiated with visible light. The ZnO with oxygen vacancies are found to be efficient for photodecomposition of 2,4-dichlorophenol under visible light irradiation.

1,213 citations

Journal ArticleDOI
TL;DR: Recent advances and emerging strategies in tailoring BiOX (X = Cl, Br, I) nanostructures to boost their photocatalytic properties are surveyed.
Abstract: Heterogeneous photocatalysis that employs photo-excited semiconductor materials to reduce water and oxidize toxic pollutants upon solar light irradiation holds great prospects for renewable energy substitutes and environmental protection. To utilize solar light effectively, the quest for highly active photocatalysts working under visible light has always been the research focus. Layered BiOX (X = Cl, Br, I) are a kind of newly exploited efficient photocatalysts, and their light response can be tuned from UV to visible light range. The properties of semiconductors are dependent on their morphologies and compositions as well as structures, and this also offers the guidelines for design of highly-efficient photocatalysts. In this review, recent advances and emerging strategies in tailoring BiOX (X = Cl, Br, I) nanostructures to boost their photocatalytic properties are surveyed.

952 citations

Journal ArticleDOI
Yandong Ma1, Ying Dai1, Meng Guo1, Chengwang Niu1, Yingtao Zhu1, Baibiao Huang1 
27 Jan 2012-ACS Nano
TL;DR: 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.
Abstract: 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.

731 citations

Journal ArticleDOI
TL;DR: This article surveys various plasmonic photocatalysts that have been prepared and characterized in recent years and describes the metal-semiconductor composite photocatalysis, in which noble metal nanoparticles are deposited on the surface of polar semiconductor or insulator particles.
Abstract: The efforts to produce photocatalysts operating efficiently under visible light have led to a number of plasmonic photocatalysts, in which noble metal nanoparticles are deposited on the surface of polar semiconductor or insulator particles. In the metal–semiconductor composite photocatalysts, the noble metal nanoparticles act as a major component for harvesting visible light due to their surface plasmon resonance while the metal–semiconductor interface efficiently separates the photogenerated electrons and holes. In this article, we survey various plasmonic photocatalysts that have been prepared and characterized in recent years.

714 citations


Cited by
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Journal ArticleDOI
TL;DR: Approaches to Modifying the Electronic Band Structure for Visible-Light Harvesting and its Applications d0 Metal Oxide Photocatalysts 6518 4.4.1.
Abstract: 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

6,332 citations

Journal ArticleDOI
TL;DR: It is anticipated that this review can stimulate a new research doorway to facilitate the next generation of g-C3N4-based photocatalysts with ameliorated performances by harnessing the outstanding structural, electronic, and optical properties for the development of a sustainable future without environmental detriment.
Abstract: As a fascinating conjugated polymer, graphitic carbon nitride (g-C3N4) has become a new research hotspot and drawn broad interdisciplinary attention as a metal-free and visible-light-responsive photocatalyst in the arena of solar energy conversion and environmental remediation. This is due to its appealing electronic band structure, high physicochemical stability, and “earth-abundant” nature. This critical review summarizes a panorama of the latest progress related to the design and construction of pristine g-C3N4 and g-C3N4-based nanocomposites, including (1) nanoarchitecture design of bare g-C3N4, such as hard and soft templating approaches, supramolecular preorganization assembly, exfoliation, and template-free synthesis routes, (2) functionalization of g-C3N4 at an atomic level (elemental doping) and molecular level (copolymerization), and (3) modification of g-C3N4 with well-matched energy levels of another semiconductor or a metal as a cocatalyst to form heterojunction nanostructures. The constructi...

5,054 citations

Journal ArticleDOI
TL;DR: More than twenty 2D carbides, nitrides and carbonitrides of transition metals (MXenes) have been synthesized and studied, and dozens more predicted to exist.
Abstract: The family of 2D transition metal carbides, carbonitrides and nitrides (collectively referred to as MXenes) has expanded rapidly since the discovery of Ti3C2 in 2011. The materials reported so far always have surface terminations, such as hydroxyl, oxygen or fluorine, which impart hydrophilicity to their surfaces. About 20 different MXenes have been synthesized, and the structures and properties of dozens more have been theoretically predicted. The availability of solid solutions, the control of surface terminations and a recent discovery of multi-transition-metal layered MXenes offer the potential for synthesis of many new structures. The versatile chemistry of MXenes allows the tuning of properties for applications including energy storage, electromagnetic interference shielding, reinforcement for composites, water purification, gas- and biosensors, lubrication, and photo-, electro- and chemical catalysis. Attractive electronic, optical, plasmonic and thermoelectric properties have also been shown. In this Review, we present the synthesis, structure and properties of MXenes, as well as their energy storage and related applications, and an outlook for future research. More than twenty 2D carbides, nitrides and carbonitrides of transition metals (MXenes) have been synthesized and studied, and dozens more predicted to exist. Highly electrically conductive MXenes show promise in electrical energy storage, electromagnetic interference shielding, electrocatalysis, plasmonics and other applications.

4,745 citations

Journal ArticleDOI
TL;DR: This paper presents a meta-analyses of the chiral stationary phase transition of Na6(CO3)(SO4)2, Na2SO4, and Na2CO3 of the Na2O/Na2O 2 mixture at the stationary phase and shows clear patterns in the response of these two materials to each other.
Abstract: Jenny Schneider,*,† Masaya Matsuoka,‡ Masato Takeuchi,‡ Jinlong Zhang, Yu Horiuchi,‡ Masakazu Anpo,‡ and Detlef W. Bahnemann*,† †Institut fur Technische Chemie, Leibniz Universitaẗ Hannover, Callinstrasse 3, D-30167 Hannover, Germany ‡Faculty of Engineering, Osaka Prefecture University, 1 Gakuen-cho, Sakai Osaka 599-8531, Japan Key Lab for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, Shanghai 200237, China

4,353 citations