Self-ordering electrochemistry: a review on growth and functionality of TiO2nanotubes and other self-aligned MOx structures
Literature Information
Andrei Ghicov, Patrik Schmuki
Among all one dimensional nanostructures other than carbon, titania nanotubes have gained increasingly more scientific interest due to a successful combination of functional material properties with a well controllable nano-architecture. For self-organized TiO2nanotube arrays not only the simple increase in the specific surface area but also their self-aligned nature leads to a significant enhancement of the performance when used in photoelectrochemistry, photocatalysis, dye-sensitized solar cells, or electrochromic devices. In addition to this, these ordered and size-controlled nanostructured TiO2 surfaces also have material-specific advantages, for example in superhydrophobic/superhydrophilic and biomedical applications. The formation of these vertically oriented nanotube arrays can be achieved by a simple one-step electrochemical self-assembly process. By adjusting the anodization parameters, the geometry such as the tube length or diameter can easily be controlled. The present review addresses the formation, properties and applications not only of TiO2nanotubes but also of related transition metal oxides.
Recommended Journals

Saudi Pharmaceutical Journal

Current Opinion in Colloid & Interface Science

Russian Journal of Organic Chemistry

Russian Journal of General Chemistry

New Journal of Chemistry

Drug Discovery Today

Journal of Peptide Science

Russian Journal of Applied Chemistry

Current Opinion in Solid State & Materials Science

Journal of Natural Medicines
Related Literature
Design of efficient methanol impermeable membranes for fuel cell applications
F. Lufrano, V. Baglio, O. Di Blasi, P. Staiti, V. Antonucci, A. S. Aricò
DOI: 10.1039/C2CP23477G
HERFD XAS/ATR-FTIR batch reactor cell
Martin Makosch, Christiane Kartusch, Jacinto Sá, Renata Bessa Duarte, Kristina Kvashnina, Pieter Glatzel, Daniel L. A. Fernandes, Maarten Nachtegaal, Jakub Szlachetko, Bobby Neuhold, Konrad Hungerbühler
DOI: 10.1039/C1CP21933B
Full structural and electrochemical characterization of Li2Ti6O13 as anode for Li-ion batteries
J. C. Pérez-Flores, C. Baehtz, M. Hoelzel, A. Kuhn, F. García-Alvarado
DOI: 10.1039/C2CP23741E
A large sample volume magic angle spinning nuclear magnetic resonance probe for in situ investigations with constant flow of reactants
Jian Zhi Hu, Jesse A. Sears, Hardeep S. Mehta, Joseph J. Ford, Ja Hun Kwak, Kake Zhu, Yong Wang, Jun Liu, David W. Hoyt, Charles H. F. Peden
DOI: 10.1039/C1CP22692D
Kinetic model for supercritical water gasification of algae
Chaohai Wei, Phillip E. Savage
DOI: 10.1039/C2CP23792J
Water ice nanoparticles: size and temperature effects on the mid-infrared spectrum
Chris Medcraft, Don McNaughton, Chris D. Thompson, Dominique R. T. Appadoo, Sigurd Bauerecker, Evan G. Robertson
DOI: 10.1039/C3CP43974G
Low-temperature combustion chemistry of biofuels: pathways in the initial low-temperature (550 K–750 K) oxidation chemistry of isopentanol‡
Oliver Welz, Judit Zádor, John D. Savee, Martin Y. Ng, Giovanni Meloni, Leonid Sheps, Taek Soon Lee, David L. Osborn, Craig A. Taatjes
DOI: 10.1039/C2CP23248K
The soft X-ray absorption spectrum of the allyl free radical
M. Alagia, E. Bodo, S. Falcinelli, R. Richter
DOI: 10.1039/C2CP43466K
Dissociation energies of X–H bonds in amino acids
Benjamin N. Moore, Ryan R. Julian
DOI: 10.1039/C2CP23443B
You might also like
How should 2-Methylbenzene-1,4-diamine dihydrochloride (CAS: 615-45-2) be stored?
2-Methylbenzene-1,4-diamine dihydrochloride (CAS: 615-45-2) should be stored in ...
Is (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide (CAS: 132747-20-7) safe?
(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide is generally considered sa...
What industries use (6-Chloropyridazin-3-YL)methanamine (CAS: 871826-15-2)?
(6-Chloropyridazin-3-YL)methanamine finds applications in the pharmaceutical ind...
What are the main uses of 2-Fluoro-3-methylphenol (CAS: 77772-72-6)?
2-Fluoro-3-methylphenol is primarily used in the synthesis of pharmaceuticals, p...
What precautions should be taken when handling 3-Methoxy-4-nitrobenzonitrile (CAS: 177476-75-4)?
When handling 3-Methoxy-4-nitrobenzonitrile, it is important to wear appropriate...
What precautions should be taken when handling 1,3-Oxazolo[4,5-b]pyridine-2(3H)-thione (CAS: 211949-57-4)?
When handling 1,3-Oxazolo[4,5-b]pyridine-2(3H)-thione (CAS: 211949-57-4), it is ...
What regulatory guidelines apply to 4-Ethynylbenzamide (CAS: 90347-86-7)?
4-Ethynylbenzamide (CAS: 90347-86-7) falls under various regulatory guidelines i...
What are the main uses of 3-(2-Ethylphenyl)-2-thioxo-4-imidazolidinone (CAS: 186822-57-1)?
3-(2-Ethylphenyl)-2-thioxo-4-imidazolidinone is primarily used as an intermediat...
What is (2-Fluoro-6-methoxyphenyl)acetic acid (CAS: 500912-19-6)?
(2-Fluoro-6-methoxyphenyl)acetic acid, also known as 4-fluoro-3-methoxybenzoic a...
What is the market or research trend for 2-[4-(Hydroxymethyl)phenoxy]ethanol (CAS: 102196-18-9)?
Market trends for 2-[4-(Hydroxymethyl)phenoxy]ethanol (CAS: 102196-18-9) indicat...
Source Journal
Chemical Communications

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry




![trans-2-{[(Tert-butoxy)carbonyl]amino}cyclobutane-1-carboxylic acid structure trans-2-{[(Tert-butoxy)carbonyl]amino}cyclobutane-1-carboxylic acid structure](https://static.chemtradehub.com/structs/951/951173-25-4-27cd.webp)