Substituent and anchor group effects in bonding to TiO2 Single Crystal Surfaces: Enhancing Solar Conversion Efficiency and Corrosion Inhibition.

Lead Research Organisation: University of Manchester
Department Name: Materials

Abstract

With concerns over the environmental impact of fossil fuel use and the issue of sustainability of fossil fuels, generation of fuels such as hydrogen or methanol and direct generation of electricity from nanoengineered materials is an area of considerable interest. Titanium dioxide (TiO2), for example, has long been known to be capable of producing hydrogen from water under illumination and can also be used to generate a photo voltage. However TiO2 absorbs in the ultraviolet region of the electromagnetic spectrum, and the amount of ultraviolet at the earth's surface is relatively low, when compared to visible light. One approach to enhance absorption of visible light is to functionalise the oxide with a material which will absorb in the visible region of the solar spectrum followed by charge transfer to the TiO2 which then drives the photoelectrochemical reaction or produces the photovoltage. This has led to the advent of dye sensitised solar cells, or the so called Graetzel cell which have an efficiency of around 15 %. These dyes are often bound to the nano structured TiO2 by carboxylic acid (COOH) groups to form Ti-O-C-O-Ti + H at the surface. The ordering, and therefore the packing density, and strength of bonding thought to play a part in the efficiency of the cells, since ultimately they control the charge transfer from the dye to the surface. Defects in the TiO2 substrate are also thought to contribute to limitations in efficiency.

Changing the chemistry of substituent groups on benzoic acids affects the acidity of the carboxyl group, and make it more or less likely to give up its proton when it attaches to the oxide material. We wish to study whether this change in the acidity has an effect on the boding strength of the molecules. We also wish to investigate whether having three oxygen atoms, as found in phosphonic acid (R-P=O(OH)2) where R is an organic side chain or ring (here we will study R=C6H5).

Synchrotron radiation allows us to utilise tunable X-rays to determine the geometry of the molecules when they are adsorbed on the surface. It also allows us to look at where the electrons are in the material and recently we discovered that we can "see" electrons being injected into the TiO2 substrate when a dye-molecule is attached to the surface, via a spectroscopic fingerprint. We wish to use this fingerprint to determine how efficiently charge is injected into the surface. In addition the techniques available at the synchrotron allow us to determine the chemistry of the molecule, and importantly its stability. Clearly any dye molecule must remain stable in order for a device to work, and loss of the bonding to the substrate would have a negative impact. This fundamental work should allow chemists designing dyes to choose the most appropriate side groups to ensure strong bonding to the TiO2 and to obtain the maximum efficiency for a particular dye.

Planned Impact

Improving the photoactivity of titania, particularly with regard to shifting the absorption into the visible region, could potentially lead to cheap water splitting catalysts to form hydrogen and oxygen using sunlight. Clearly the use of hydrogen is an attractive means by which to reducing fossil fuel consumption. In addition, titania is being widely investigated and indeed used for the cleaning of wastewater, acting both as a bactericide and also in the degradation of organic pollutants. Since titania is cheap this potentially impacts on the costs of waste water treatment and may benefit developing countries where access to clean drinking water is limited. Finally the molecules of interest in this proposal are related to similar molecules being investigated for in flow corrosion inhibition in steel.

UK chemical companies may benefit from the research in that cheap photocatalysts capable of "cleaning" effluent before discharge back to the water supply will cut their costs both in UK and overseas facilities. These two points alone will lead to reduced costs in providing a cleaner and greener global economy. Oil companies would benefit from enhanced corrosion control, again, reducing waste in the downstream oil industry will aid in a greener economy and in keeping fuel costs down. It will also ensure that we are able continue to provide supplies of oil for synthons in polymer industry as well as fuel by minimising waste.

More directly the research itself will provide direct training in the use of low energy synchrotron radiation techniques to two UK postgraduate students. These facilities are currently not available in the UK so this type of training is invaluable to the next generation of surface science and catalysis researchers to ensure these skills are not lost, particularly when the new beam lines at the Diamond Light source become open to users over the next two years.

Publications

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Wagstaffe M (2016) Ionic Liquid Ordering at an Oxide Surface. in Chemphyschem : a European journal of chemical physics and physical chemistry

 
Description The proposed research covered a number of important areas concerned with functionalisation of oxide materials and corrosion inhibition. We studied the interaction of a number of molecules with titanium dioxide and iron surfaces. We found that phosphonic acids bond to the surface of anatase titanium dioxide through two oxygen atoms. This confirmed theoretical predictions for the surface. We also showed that the acid forms a stable and ordered overlayer and thus offers an alternative to carboxylic acids for the functionalisation of titania surfaces. This has potential applications in healthcare, hybrid photovoltaic cells and photocatalysis. The work on iron surfaces shows that phosphonate bond strongly to the surface through three oxygen atoms and again form an ordered and stable layer on the surface. This suggests phosphonate corrosion inhibitors interact with the metal surface itself rather than a native oxide layer. Further work is underway in order to confirm this. We have also looked at the interaction of novel electrolytes, ionic liquids with titanium dioxide surfaces. This work is linked to the anodic growth of titania nanostructures which are of interest in photocatalytic water splitting and also to the development of new battery systems,
Exploitation Route We have already started to look at the interaction of ionic liguids supported on TiO2 and ZnO with water and CO2 using near-ambient pressure X-ray photoelectron spectroscopy. I will submit an application to EPSRC with other UK researchers to take this study forward since it may be utilised as a method for photo catalysed reactions of water and CO2 for methanol synthesis. We have recently begun preliminary investigation of reaction of pollutant gases with molecularly functionalised titania with Croda Healthcare which we hope will lead to new products.
Sectors Chemicals,Energy,Healthcare

URL http://pubs.acs.org/doi/abs/10.1021/acs.jpcc.5b11258
 
Description Cafe Scientifique 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach Regional
Primary Audience Public/other audiences
Results and Impact Talk on research in the area of functionalisation/ molecular interaction with surfaces with some results associated with this funding.
Year(s) Of Engagement Activity 2016