Research Progress on Catalytic Water Splitting Based on Polyoxometalate/Semiconductor Composites
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Application of the Photocatalytic Chemistry of Titanium Dioxide to Disinfection and the Killing of Cancer Cells
Separation and Purification Methods Volume 28(1) 1999, pp. 1-50 APPLICATION OF THE PHOTOCATALYTIC CHEMISTRY OF TITANIUM DIOXIDE TO DISINFECTION AND THE KILLING OF CANCER CELLS Daniel M. Blake, Pin-Ching Maness, Zheng Huang, Edward J. Wolfrum, and Jie Huang The National Renewable Laboratory 1617 Cole Boulevard Golden, Colorado 80401-3393 William A. Jacoby Department of Chemical Engineering W2016 Engineering Building East University of Missouri Columbia, MO 65211 Table of Contents Abstract........................................................................................................................... 2 Introduction .................................................................................................................... 2 Background..................................................................................................................... 3 Mode of Action of TiO2................................................................................................... 6 Photocatalytic Reactor Configurations .......................................................................... 9 Structure of Target Organisms....................................................................................... 10 Bacteria...................................................................................................................... 10 Viruses ....................................................................................................................... 13 Fungi......................................................................................................................... -
Application of Titanium Dioxide Photocatalysis to Create Self-Cleaning Building Materials
Application of Titanium Dioxide Photocatalysis to Create Self-Cleaning Building Materials Roland Benedix1 Frank Dehn2 Jana Quaas, Marko Orgass3 SUMMARY To realize self-cleaning material surfaces there are two principal ways: the de- velopment of super-hydrophobic or super-hydrophilic materials. By transferring the microstructure of selected plant surfaces to practical materials like tiles and facade paints, super-hydrophobic surfaces were obtained (Lotus effect). Super- hydrophilic materials were developed by coating glass, ceramic tiles or plastics with the semiconducting photocatalyst titanium dioxide (TiO2). If TiO2 is illumi- nated by light, grease, dirt and organic contaminants are decomposed and can easily be swept away by water (rain). Subject of our further research is a detailed study of the interaction between TiO2 and traditional building materials like con- crete, mortar and plaster. 1 INTRODUCTION In practice, surface cleaning of building materials like tiles, facades and glass panes causes considerable trouble, high consumption of energy and chemical detergents and, consequently, high costs. To realize self-cleaning material sur- faces there are two principal ways: the development of so-called super- hydrophobic or super-hydrophilic surfaces. 1 Prof. Dr. rer. nat. habil., FB IMN/Chemie, HTWK Leipzig 2 Dipl.-Ing., Institut für Massivbau und Baustofftechnologie, Universität Leipzig 3 cand.-Ing., Institut für Massivbau und Baustofftechnologie, Universität Leipzig 157 LACER No. 5, 2000 The wetting of a solid with water, where air is the surrounding medium, is de- pendent on the relation between the interfacial tensions (water/air, water/solid and solid/air). The ratio between these tensions determines the contact angle θ be- tween a water droplet on a given surface. -
Vanadium(V)-Substitution Reactions of Wells–Dawson-Type 6− Polyoxometalates: from [X2M18O62] (X = P, As; M = Mo, W) 7− to [X2VM17O62]
Inorganics 2015, 3, 355-369; doi:10.3390/inorganics3030355 OPEN ACCESS inorganics ISSN 2304-6740 www.mdpi.com/journal/inorganics Article Vanadium(V)-Substitution Reactions of Wells–Dawson-Type 6− Polyoxometalates: From [X2M18O62] (X = P, As; M = Mo, W) 7− to [X2VM17O62] Tadaharu Ueda *, Yuriko Nishimoto, Rie Saito, Miho Ohnishi and Jun-ichi Nambu Department of Applied Science, Faculty of Science, Kochi University, Kochi 780-8520, Japan * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +81-88-844-8299; Fax: +81-88-844-8359. Academic Editors: Greta Ricarda Patzke and Pierre-Emmanuel Car Received: 14 April 2015 / Accepted: 25 June 2015 / Published: 14 July 2015 Abstract: The formation processes of V(V)-substituted polyoxometalates with the Wells–Dawson-type structure were studied by cyclic voltammetry and by 31P NMR and Raman spectroscopy. Generally, the vanadium-substituted heteropolytungstates, 7− 7− [P2VW17O62] and [As2VW17O62] , were prepared by mixing equimolar amounts of the 10− 10− corresponding lacunary species—[P2W17O61] and [As2W17O61] —and vanadate. According to the results of various measurements in the present study, the tungsten site in 6− 6− the framework of [P2W18O62] and [As2W18O62] without defect sites could be substituted 7− 7− with V(V) to form the [P2VW17O62] and [As2VW17O62] , respectively. The order in which the reagents were mixed was observed to be the key factor for the formation of Dawson-type V(V)-substituted polyoxometalates. Even when the concentration of each reagent was identical, the final products differed depending on the order of their addition to the reaction mixture. Unlike Wells–Dawson-type heteropolytungstates, the molybdenum sites in the 6− 6− framework of [P2Mo18O62] and [As2Mo18O62] were substituted with V(V), but formed 4− 4− 7− Keggin-type [PVMo11O40] and [AsVMo11O40] instead of [P2VMo17O62] and 7− [As2VMo17O62] , respectively, even though a variety of reaction conditions were used. -
Polyoxometalate Bleaching of Kraft Pulp
In: Proceedings of the 1995 TAPPI Pulping conference; 1995 October 1-5; Chicago, IL. Atlanta, GA: TAPPI PRESS: 153-156.Book 1. POLYOXOMETALATE BLEACHING OF KRAFT used in kraft pulping is envisioned. In bleaching. fully oxidized PULP: A HIGHLY SELECTIVE CLOSED MILL POM complexes are reacted with unbleached pulp under anaerobic TECHNOLOGY. conditions. During oxidative bleaching. the POM complexes are reduced and oxidized residual lignin fragments are dissolved by the I. A. Weinstock, R. H. Atalla. R. S. Reiner, M. A. Moen bleaching liquor. Afterwards, the reduced POM liquor is reoxidized and K. E. Hammel by oxygen under conditions that convert dissolved lignin fragments USDA Forest Service. to carbon dioxide and water. Thus, the POM liquor can be Forest Products Laboratory1 continually reused with mill closure achieved by use of a recovery Madison, Wisconsin U.S.A. system, in which. analogously to the kraft recovery system. active POM liquors are reactivated and organic materials consumed. C. L. Hill C. J. Houtman Emory University University of Wisconsin-Madison Closed Mill Polyoxometalate Blenching Process Department of Chemistry DepartmentofChemical Engineering Atlanta, Georgia U.S.A. Madison, Wisconsin. U.S.A. ABSTRACT A process for using polyoxometalate (POM) salts and oxygen in the commercial bleaching of chemical pulps is herein described. A clear advantage of polyoxometalates over oxygen alone. hydrogen peroxide or ozone is their inherently high oxidative selectivity for the residual lignin in softwood kraft pulps. Softwood kraft pulps delignified to low kappa numbers using POM salts possess Figure 1. Schematic diagram of an effluent-free papermaking properties comparable to those obtained using polyoxometalate bleaching process. -
(Hetero)Polyoxometalates for Simultaneously
(19) TZZ¥__T (11) EP 3 175 867 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.: 07.06.2017 Bulletin 2017/23 A61L 2/232 (2006.01) A47J 31/44 (2006.01) A01N 25/10 (2006.01) A01N 59/16 (2006.01) (2006.01) (2006.01) (21) Application number: 15197882.2 A61L 2/238 C02F 1/72 C09D 5/16 (2006.01) D06F 35/00 (2006.01) (2006.01) (2006.01) (22) Date of filing: 03.12.2015 F24C 15/00 F24C 15/20 H05B 6/64 (2006.01) A47L 15/42 (2006.01) A61L 2/235 (2006.01) A61L 9/18 (2006.01) C08K 5/00 (2006.01) C08K 5/56 (2006.01) C02F 103/00 (2006.01) (84) Designated Contracting States: (72) Inventors: AL AT BE BG CH CY CZ DE DK EE ES FI FR GB • SCHEPERS, Klaus GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO 35619 Braunfels (DE) PL PT RO RS SE SI SK SM TR • MISCHO, Horst Designated Extension States: 54295 Trier (DE) BA ME • BIRKEL, Alexander Designated Validation States: 64287 Darmstadt (DE) MA MD (74) Representative: Teipel, Stephan et al (71) Applicant: POM Patentverwaltungs GbR Lederer & Keller 35619 Braunfels (DE) Patentanwälte Partnerschaft mbB Unsöldstrasse 2 80538 München (DE) (54) USE OF (HETERO)POLYOXOMETALATES FOR SIMULTANEOUSLY IMPARTING ANTIMICROBIAL PROPERTIES TO A SURFACE OF A SUBSTRATE AND REDUCING THE GROWTH OF A BIOFILM ON THE SURFACE OF THE SUBSTRATE (57) The present invention relates to the use of at a substrate comprising a (hetero)polyoxometalate or a leastone (hetero)polyoxometalate for simultaneously im- mixture of (hetero)polyoxometalates, wherein the sub- partingantimicrobial propertiesto a surface ofa substrate strate is selected from a polymer body, paint, varnish and and reducing the growth of a biofilm on the surface of the coating. -
The Highly Efficient Photocatalytic and Light Harvesting Property of Ag-Tio2
www.nature.com/scientificreports OPEN The highly efcient photocatalytic and light harvesting property of Ag-TiO2 with negative nano-holes Received: 3 October 2017 Accepted: 24 November 2017 structure inspired from cicada wings Published: xx xx xxxx Imran Zada1, Wang Zhang1, Wangshu Zheng1, Yuying Zhu1, Zhijian Zhang2, Jianzhong Zhang2, Muhammad Imtiaz1, Waseem Abbas1 & Di Zhang1 The negative replica of biomorphic TiO2 with nano-holes structure has been efectively fabricated directly from nano-nipple arrays structure of cicada wings by using a simple, low-cost and highly efective sol-gel ultrasonic method. The nano-holes array structure was well maintained after calcination in air at 500 °C. The Ag nanoparticles (10 nm–25 nm) were homogeneously decorated on the surface and to the side wall of nano-holes structure. It was observed that the biomorphic Ag-TiO2 showed remarkable photocatalytic activity by degradation of methyl blue (MB) under UV-vis light irradiation. The biomorphic Ag-TiO2 with nano-holes structure showed superior photocatalytic activity compared to the biomorphic TiO2 and commercial Degussa P25. This high-performance photocatalytic activity of the biomorphic Ag-TiO2 may be attributed to the nano-holes structure, localized surface plasmon resonance (LSPR) property of the Ag nanoparticles, and enhanced electron-hole separation. Moreover, the biomorphic Ag-TiO2 showed more absorption capability in the visible wavelength range. This work provides a new insight to design such a structure which may lead to a range of novel applications. Photolysis of organic containments has paid a great attention in environmental cleaning and water purifcation1–5. TiO2 has been extensively used as a photocatalytic material due to its signifcant photostability, environmentally friendliness, high chemical stability, non-toxicity and low-cost6. -
Hybrid Organic-Inorganic Materials Based on Polyoxometalates and Ionic Liquids and Their Application in Catalysis
Hindawi Publishing Corporation ISRN Chemical Engineering Volume 2014, Article ID 963792, 13 pages http://dx.doi.org/10.1155/2014/963792 Review Article Hybrid Organic-Inorganic Materials Based on Polyoxometalates and Ionic Liquids and Their Application in Catalysis Svetlana Ivanova Departamento de Qu´ımica Inorganica´ e Instituto de Ciencia de Materiales de Sevilla, Centro Mixto Universidad de Sevilla-CSIC, Avenida AmericoVespucio49,41092Sevilla,Spain´ Correspondence should be addressed to Svetlana Ivanova; [email protected] Received 2 October 2013; Accepted 7 November 2013; Published 28 January 2014 Academic Editors: P. Maki-Arvela,¨ A. Ragauskas, and A. M. Seayad Copyright © 2014 Svetlana Ivanova. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. An overview of the recent advances in the field of polyoxometalate, ionic liquid hybrids, is proposed with a special attention paid to their application in catalysis, more precisely biphasic and heterogeneous catalysis. Both components of the hybrids are separately outlined pointing to their useful properties and potential for catalysis, followed by the description of the hybrids preparation and synergy between components in a large range of organic transformations. And finally a vision on the future developments is proposed. 1. Polyoxometalates: General Aspects [6–9]. There are literally thousands of compounds in the polyoxometalate category which defers on their size, shape, Polyoxometalates (POMs) are a class of anionic metal-oxygen and composition. Recently, Long et al. [10]proposedavery clusters built by the connection of [MO] polyhedra of elegant way to classify the POM’s compounds in-as-called the early transition metals in their highest oxidation states “polyoxometalate periodic table.” Th e y prop o s e d t h re e bro a d [1, 2]. -
The Reactivity and Stability of Polyoxometalate Water Oxidation Electrocatalysts
molecules Review The Reactivity and Stability of Polyoxometalate Water Oxidation Electrocatalysts Dandan Gao 1, Ivan Trentin 1, Ludwig Schwiedrzik 2 , Leticia González 2,* and Carsten Streb 1,3,* 1 Institute of Inorganic Chemistry I, Ulm University, Albert-Einstein-Allee 11, 89081 Ulm, Germany; [email protected] (D.G.); [email protected] (I.T.) 2 Institute of Theoretical Chemistry, Faculty of Chemistry, University of Vienna, Währinger Str. 17, 1090 Vienna, Austria; [email protected] 3 Helmholtz-Institute Ulm (HIU), Helmholtzstr. 11, 89081 Ulm, Germany * Correspondence: [email protected] (L.G.); [email protected] (C.S.) Academic Editor: Mark Symes Received: 4 December 2019; Accepted: 27 December 2019; Published: 31 December 2019 Abstract: This review describes major advances in the use of functionalized molecular metal oxides (polyoxometalates, POMs) as water oxidation catalysts under electrochemical conditions. The fundamentals of POM-based water oxidation are described, together with a brief overview of general approaches to designing POM water oxidation catalysts. Next, the use of POMs for homogeneous, solution-phase water oxidation is described together with a summary of theoretical studies shedding light on the POM-WOC mechanism. This is followed by a discussion of heterogenization of POMs on electrically conductive substrates for technologically more relevant application studies. The stability of POM water oxidation catalysts is discussed, using select examples where detailed data is already available. The review finishes with an outlook on future perspectives and emerging themes in electrocatalytic polyoxometalate-based water oxidation research. Keywords: polyoxometalate; water oxidation catalysis; oxygen evolution reaction; self-assembly; electrocatalysis 1. -
Applications of Polyoxometalates in Heterogenous Catalysis Piotr Putaj
Applications of polyoxometalates in heterogenous catalysis Piotr Putaj To cite this version: Piotr Putaj. Applications of polyoxometalates in heterogenous catalysis. Other. Université Claude Bernard - Lyon I, 2012. English. NNT : 2012LYO10038. tel-00869429 HAL Id: tel-00869429 https://tel.archives-ouvertes.fr/tel-00869429 Submitted on 3 Oct 2013 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. N° d’ordre 38-2012 Année 2012 THESE DE L‘UNIVERSITE DE LYON délivrée par L’UNIVERSITE CLAUDE BERNARD LYON 1 ECOLE DOCTORALE DE CHIMIE DIPLOME DE DOCTORAT (arrêté du 7 août 2006) soutenue publiquement le 21/03/2012 par M. Piotr Putaj Applications des polyoxométalates en catalyse hétérogène Directeur de thèse : M. Frédéric Lefebvre Jury : M. Stéphane Daniele (Président) Mme Catherine Marchal-Roch M. Régis Gauvin M. Richard Villanneau M. José M. Fraile M. Frédéric Lefebvre N° d’ordre 38-2012 Année 2012 THESE DE L‘UNIVERSITE DE LYON délivrée par L’UNIVERSITE CLAUDE BERNARD LYON 1 ECOLE DOCTORALE DE CHIMIE DIPLOME DE DOCTORAT (arrêté du 7 août 2006) soutenue publiquement le 21/03/2012 par M. Piotr Putaj Applications of polyoxometalates in heterogenous catalysis Directeur de thèse : M. -
Photodehydrogenation of Ethanol Over Cu2o/Tio2 Heterostructures
nanomaterials Article Photodehydrogenation of Ethanol over Cu2O/TiO2 Heterostructures Congcong Xing 1,2, Yu Zhang 1, Yongpeng Liu 3 , Xiang Wang 1, Junshan Li 1, Paulina R. Martínez-Alanis 4 , Maria Chiara Spadaro 5 , Pablo Guardia 1, Jordi Arbiol 5,6 , Jordi Llorca 2,* and Andreu Cabot 1,6,* 1 Catalonia Institute for Energy Research (IREC), Sant Adrià de Besòs, 08930 Barcelona, Spain; [email protected] (C.X.); [email protected] (Y.Z.); [email protected] (X.W.); [email protected] (J.L.); [email protected] (P.G.) 2 Institute of Energy Technologies, Department of Chemical Engineering and Barcelona Research Center in Multiscale Science and Engineering, Universitat Politècnica de Catalunya, EEBE, 08019 Barcelona, Spain 3 Laboratory for Molecular Engineering of Optoelectronic Nanomaterials (LIMNO), École Polytechnique Fédérale de Lausanne (EPFL), Station 6, CH-1015 Lausanne, Switzerland; yongpeng.liu@epfl.ch 4 ENFOCAT-IN2UB, Universitat de Barcelona (UB), C/Martí i Franquès 1, 08028 Barcelona, Spain; [email protected] 5 Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and BIST, Campus UAB, Bellaterra, 08193 Barcelona, Spain; [email protected] (M.C.S.); [email protected] (J.A.) 6 ICREA, Pg. Lluis Companys 23, 08010 Barcelona, Spain * Correspondence: [email protected] (J.L.); [email protected] (A.C.) Abstract: The photodehydrogenation of ethanol is a sustainable and potentially cost-effective strategy to produce hydrogen and acetaldehyde from renewable resources. The optimization of this process requires the use of highly active, stable and selective photocatalytic materials based on abundant elements and the proper adjustment of the reaction conditions, including temperature. -
Metal-Organic Frameworks with Photocatalytic Bactericidal Activity for Integrated Air Cleaning
ARTICLE https://doi.org/10.1038/s41467-019-10218-9 OPEN Metal-organic frameworks with photocatalytic bactericidal activity for integrated air cleaning Ping Li1, Jiazhen Li1, Xiao Feng1, Jie Li1, Yuchen Hao1, Jinwei Zhang1, Hang Wang1, Anxiang Yin1, Junwen Zhou1, Xiaojie Ma1 & Bo Wang 1 Air filtration has become an essential need for passive pollution control. However, most of the commercial air purifiers rely on dense fibrous filters, which have good particulate matter 1234567890():,; (PM) removal capability but poor biocidal effect. Here we present the photocatalytic bac- tericidal properties of a series of metal-organic frameworks (MOFs) and their potentials in air pollution control and personal protection. Specifically, a zinc-imidazolate MOF (ZIF-8) exhibits almost complete inactivation of Escherichia coli (E. coli) (>99.9999% inactivation efficiency) in saline within 2 h of simulated solar irradiation. Mechanistic studies indicate that photoelectrons trapped at Zn+ centers within ZIF-8 via ligand to metal charge transfer (LMCT) are responsible for oxygen-reduction related reactive oxygen species (ROS) pro- duction, which is the dominant disinfection mechanism. Air filters fabricated from ZIF-8 show remarkable performance for integrated pollution control, with >99.99% photocatalytic killing efficiency against airborne bacteria in 30 min and 97% PM removal. This work may shed light on designing new porous solids with photocatalytic antibiotic capability for public health protection. 1 Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, Key Laboratory of Cluster Science, Ministry of Education, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, 100081 Beijing, China. Correspondence and requests for materials should be addressed to X.M. -
Ion-Pairing in Polyoxometalate Chemistry: Impact of Fully Hydrated Alkali Metal Cations on Properties of the Keggin 3- [PW12O40] Anion
Dalton Transactions Ion-Pairing in Polyoxometalate Chemistry: Impact of Fully Hydrated Alkali Metal Cations on Properties of the Keggin 3- [PW12O40] Anion Journal: Dalton Transactions Manuscript ID DT-ART-06-2020-002239.R1 Article Type: Paper Date Submitted by the 14-Jul-2020 Author: Complete List of Authors: Kaledin, Alexey; Emory University, Cherry L. Emerson Center for Scientific Computation Yin, Qiushi; Emory University Hill, Craig; Emory University Lian, Tianquan; Emory University Musaev, D.; Emory University Page 1 of 15 Dalton Transactions Ion-Pairing in Polyoxometalate Chemistry: Impact of Fully Hydrated Alkali 3- Metal Cations on Properties of the Keggin [PW12O40] Anion Alexey L. Kaledin,1 Qiushi Yin,2 Craig L. Hill,1,2 Tianquan Lian,1,2 and Djamaladdin G. Musaev1,2,* 1 Emerson Center for Scientific Computation, Emory University, Atlanta, Georgia 30322 USA 2 Department of Chemistry, Emory University, Atlanta, Georgia 3032 USA Abstract The counterions of polyoxometalates (POMs) impact properties and applications of this growing class of inorganic clusters. Here, we used density functional theory (DFT) to elucidate the impact of fully hydrated alkali metal cations on the geometry, electronic structure, and chemical properties 3- of the polyoxotungstate anion [PW12O40] . The calculations show that the HOMO of the free anion 3- [PW12O40] is a linear combination of the 2p AOs of the bridging oxygens, and the first few LUMOs are the 5d orbitals of the tungsten atoms. The S0 S1 electron excitation, near 3 eV, is associated with the O(2p) W(5d) transition. Anion/cation complexation leads to formation of 3- + [PW12O40] [M (H2O)16]3 ion-pair complexes, where with the increase of atomic number of M, the + M (H2O)16 cluster releases several water molecules and interacts strongly with the 3- + polyoxometalate anion.