Details of Grant 

EPSRC Reference:	EP/P006051/1
Title:	Optimisation of charge carrier mobility in nanoporous metal oxide films
Principal Investigator:	Mckenna, Professor KP
Other Investigators:	Chechik, Professor V Douthwaite, Dr R Lazarov, Professor V
Researcher Co-Investigators:
Project Partners:	Cristal Pigment UK Ltd Dyesol UK Ltd University of Tokyo
Department:	Physics
Organisation:	University of York
Scheme:	Standard Research
Starts:	01 January 2017	Ends:	31 October 2020	Value (£):	798,645
EPSRC Research Topic Classifications:	Materials Characterisation Materials Processing Materials Synthesis & Growth Solar Technology
EPSRC Industrial Sector Classifications:	Energy
Related Grants:
Panel History:	Panel Date Panel Name Outcome 21 Jul 2016 EPSRC Physical Sciences Materials - July 2016 Announced
Summary on Grant Application Form
High surface area nanoporous films formed by sintering metal oxide nanoparticles are highly stable, non-toxic and inexpensive to produce on an industrial scale. They find a wide range of applications in gas sensing and catalysis where high surface area is essential to maximise the interaction of molecules with the film. They also find applications as charge transport layers in third generation solar cells, e.g. dye- or perovskite-sensitised cells, where efficient photoinjection of electrons and holes is ensured by coating nanoporous films with a light absorbing material. For solar cells, as well as for other important applications of nanoporous films such as electrodes in fuel cells and photoelectrochemical cells, good charge carrier mobility is also an essential requirement. Unfortunately, despite their numerous advantages, the electronic mobility of nanoporous oxide films is in general very poor. For example, the mobilities of nanoporous TiO2, ZnO and SnO2 films have been shown to be between two and four orders of magnitude smaller than those of corresponding single crystals. This low mobility is a key factor limiting the efficiency of (photo-)electrochemical and photovoltaic applications and is usually attributed to increased charge carrier trapping at surfaces and at interfaces between nanoparticles. Since charge trapping is associated with ions near surfaces we hypothesise that it should be possible to eliminate these traps by suitable chemical modification of the surfaces of nanoparticles prior to sintering into a film. This approach would retain the advantages of nanoporous films in terms of high surface area, non-toxicity and processability while improving mobility. Such modifications have been attempted previously, but due to the lack of understanding on the origin of charge trapping or the effects of surface modification, success has been limited. Here, we propose to combine the predictive power of first principles theoretical modelling with structural, spectroscopic and photophysical materials characterisation, in order to quantify the factors responsible for charge trapping at surface and interfaces in nanoporous oxide films at an atomistic level. Once validated and refined on unmodified films, theoretical methods will be used to assess modification strategies to reduce charge-trapping. In particular, we will consider the incorporation/substitution of anions and cations near the surface of oxide nanoparticles to eliminate the problematic trapping sites. The ability to theoretically screen various possible modification routes (i.e. different cations and anions) is a key advantage of our proposed approach. Application, testing and optimisation of such strategies may offer a new paradigm for knowledge-led design of solar oxide materials. We aim to demonstrate the effectiveness of our approach by increasing the mobility of nanostructured TiO2 and ZrO2 to deliver an improvement in the efficiency of perovskite-sensitised solar cells, which are emerging as an attractive third generation photovoltaic technology. The size of the third generation photovoltaic market is predicted to grow to $38bn by 2022, making this an area with significant potential for economic impact. Improving the mobility of nanoporous oxides could bring the efficiency of these devices from their current level (about 20%) to closer to the theoretical maximum of about 30%. An increase in overall efficiency from 20% to only 23% percent would increase the total power output by 15%, which when coupled with lower manufacturing costs would make the technology very attractive. We will work with leading manufacturers of nano-TiO2 (Cristal) and perovskite-sensitised solar cells (Dyesol Limited) to test the performance of our modified films. More generally, the ability to tailor the electronic properties of interfaces in nanoporous films by controlled modification should find applications in other technologies including sensing, catalysis and electronics.
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