Author
Jincai Zhao
Other affiliations: Dalian University of Technology, Nanyang Technological University, Peking University ...read more
Bio: Jincai Zhao is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Photocatalysis & Photodegradation. The author has an hindex of 87, co-authored 342 publications receiving 29185 citations. Previous affiliations of Jincai Zhao include Dalian University of Technology & Nanyang Technological University.
Topics: Photocatalysis, Photodegradation, Catalysis, Visible spectrum, Chemistry
Papers published on a yearly basis
Papers
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TL;DR: In this tutorial review, the unique mechanistic characteristics, the constitution of photodegradation systems and their performance are described and the involved radical reactions during the degradation are discussed.
Abstract: The semiconductor and the surface-adsorbed antenna molecule (dyes or other color species) can constitute efficient photochemical systems for environmental remediation. The major advantage of these systems is that they are able to achieve the degradation of organic pollutants by using visible light from the sun as energy and O2 in the air as the oxidant under ambient conditions. In this tutorial review, the unique mechanistic characteristics, the constitution of photodegradation systems and their performance are described. The involved radical reactions during the degradation are also discussed.
1,974 citations
TL;DR: This review covers state-of-the-art accomplishments in visible-light-induced selective organic transformations by heterogeneous photocatalysis and discusses three sections based on the photocatalyst type: metal oxides such as TiO2, Nb2O5 and ZnO; plasmonic photocatalysts like nanostructured Au, Ag or Cu supported on metal oxide; and polymeric graphitic carbon nitride.
Abstract: The future development of chemistry entails environmentally friendly and energy sustainable alternatives for organic transformations. Visible light photocatalysis can address these challenges, as reflected by recent intensive scientific endeavours to this end. This review covers state-of-the-art accomplishments in visible-light-induced selective organic transformations by heterogeneous photocatalysis. The discussion comprises three sections based on the photocatalyst type: metal oxides such as TiO2, Nb2O5 and ZnO; plasmonic photocatalysts like nanostructured Au, Ag or Cu supported on metal oxides; and polymeric graphitic carbon nitride. Finally, recent strides in bridging the gap between photocatalysis and other areas of catalysis will be highlighted with the aim of overcoming the existing limitations of photocatalysis by developing more creative synthetic methodologies.
1,177 citations
TL;DR: The study demonstrates that the modification of TiO2 both to extend its spectral response to the visible region and to improve its catalytic efficiency can be achieved by doping with boron, a nonmetal, and Ni2O3, a metal oxide.
Abstract: To promote efficient use of solar energy, many studies have focused on the modification of TiO2 to extend its spectral response to visible region. Here we report a combined modification of TiO2 by two components: the nonmetal element boron and the metal oxide Ni2O3. The photocatalyst presents high photocatalytic activity in the visible region, which can efficiently degrade and mineralize toxic organic pollutants such as trichlorophenol (TCP), 2,4-dichlorophenol (2,4-DCP), and sodium benzoate. The dechlorination and mineralization results indicate the photocatalytic pathway via visible light excitation. The study demonstrates that the modification of TiO2 both to extend its spectral response to the visible region and to improve its catalytic efficiency can be achieved by doping with boron, a nonmetal, and Ni2O3, a metal oxide.
1,097 citations
TL;DR: In this article, the inverse photosensitized oxidative transformation of tetraethylated rhodamine (RhB) under visible illumination of aqueous titania dispersions is demonstrated.
Abstract: Chemical oxygen demand (CODCr) and proton NMR, UV−vis, and spin trapping EPR spectroscopic evidence is presented to demonstrate the inverse photosensitized oxidative transformation of tetraethylated rhodamine (RhB) under visible illumination of aqueous titania dispersions. Both de-ethylation and oxidative degradation take place with the former proceeding in a stepwise manner to yield mono-, di-, tri-, and tetra-de-ethylated rhodamine species. Intermediates present after each de-ethylation step remain in a fast dynamic equilibrium between the titania particle surface and the bulk solution. The concentration of •OH radicals, formed from the inverse photosensitization process through the superoxide radical anion, increases upon addition of the anionic dodecylbenzene sulfonate surfactant (DBS) because a larger number of RhB excited states are able to inject an electron into the conduction band of the TiO2 particles. Also, intermediates that can no longer absorb the visible light, (i.e., once the dye solution ...
948 citations
TL;DR: The aggregate of DD-PTCDI shows a pronounced absorption band at the longer wavelength, whereas the absorption of ND-P TCDI aggregate is not significant in the same wavelength region, and optical spectral observations are reminiscent of the previous theoretical investigation on the side-chain-modulated electronic properties of PTCDI assembly.
Abstract: Effect of side-chain substitutions on the morphology of self-assembly of perylene diimide molecules has been studied with two derivatives modified with distinctly different side-chains, N,N‘-di(dodecyl)-perylene-3,4,9,10-tetracarboxylic diimide (DD-PTCDI) and N,N‘-di(nonyldecyl)-perylene-3,4,9,10-tetracarboxylic diimide (ND-PTCDI). Due to the different side-chain interference, the self-assembly of the two molecules results in totally different morphologies in aggregate: one-dimensional (1D) nanobelt vs zero-dimensional (0D) nanoparticle. The size, shape, and topography of the self-assemblies were extensively characterized by a variety of microscopies including SEM, TEM, AFM, and fluorescence microscopy. The distinct morphologies of self-assembly have been obtained from both the solution-based processing and surface-supported solvent-vapor annealing. The nanobelts of DD-PTCDI fabricated in solution can feasibly be transferred to both polar (e.g., glass) and nonpolar (e.g., carbon) surfaces, implying the h...
599 citations
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9,432 citations
TL;DR: This critical review shows the basis of photocatalytic water splitting and experimental points, and surveys heterogeneous photocatalyst materials for water splitting into H2 and O2, and H2 or O2 evolution from an aqueous solution containing a sacrificial reagent.
Abstract: This critical review shows the basis of photocatalytic water splitting and experimental points, and surveys heterogeneous photocatalyst materials for water splitting into H2 and O2, and H2 or O2 evolution from an aqueous solution containing a sacrificial reagent Many oxides consisting of metal cations with d0 and d10 configurations, metal (oxy)sulfide and metal (oxy)nitride photocatalysts have been reported, especially during the latest decade The fruitful photocatalyst library gives important information on factors affecting photocatalytic performances and design of new materials Photocatalytic water splitting and H2 evolution using abundant compounds as electron donors are expected to contribute to construction of a clean and simple system for solar hydrogen production, and a solution of global energy and environmental issues in the future (361 references)
8,850 citations
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
TL;DR: The field of photocatalysis can be traced back more than 80 years to early observations of the chalking of titania-based paints and to studies of the darkening of metal oxides in contact with organic compounds in sunlight as discussed by the authors.
5,729 citations
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