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Yusuf Hamied Department of Chemistry

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Professor of Physical Chemistry

Our research interests cover a wide range of problems in colloid and interface science from adsorption of molecules to solid surfaces from liquids to the structure and behaviour of particles in complex fluids.

Adsorption from solution

The adsorption of molecules from liquids and solutions to solid surfaces is central to many areas of academic and industrial importance such as colloidal stability, lubrication, protein biofilms and making icecream. We have developed a combination of experimental methods, including coherent and incoherent neutron scattering and STM, that can provide details of the state, absolute composition and crystallographic structure of the adsorbed layers.

Currently projects are available to investigate formation of crystalline layers for a number of interesting materials and also to probe their surface mixing behaviour. In particular, we are investigating a novel 'non-covalent' interaction - 'halogen-bonding' - as a way of organising molecules on a surface. Halogen bonds can be thought of as the new hydrogen bond: they are relatively strong, directional and can be controlled by playing with the chemistry of nearby constituents. We have been successful in preparing co-crystals on a surface using these special interactions and now are using computer calculations (DFT) to understand in detail the roles of different interactions on controlling the monolayer structure. These layers form very stable mono and multilayers, materials with important industrial and biological relevance.



Figure illustrating a monolayer co-crystal held together by a halogen bond. The sigma hole is the site on the halogen (Iodine in this case) that accepts the electrons from the adjacent nitrogen on the neighbouring molecule. The halogen bonds give rise to characteristic chains of molecules in this case.

Adsorption to metal surfaces - enhancing lubrication, preventing wear and corrosion - better fuel efficiency and coating performance

We have recently developed a number of novel approaches (polarised neutron reflection, sum frequency generation non-linear optics, sensitive calorimetry etc) to investigate adsorption of particular species to the surfaces of metals and metal oxides in oils and water. These systems have major importance industrially in lubrication, wear, friction modification, implant rejection etc.. hence we have an important role to play in energy efficiency, corrosion and biomedical areas. We have been able to identify what is adsorbed at these surfaces, how much is present, what the structure of the layer is, the strength and nature of surface binding, even to the level of the conformational order of the alkyl chains of the adsorbed species. Recently we have extended this work to include the study of these interfaces under external fields such as elevated temperature and imposed shear flow. We already have some interesting results that indicate that thin (20A) molecular layers are largely unaffected by a shear flow up to 1000s-1. In contrast, much thicker(1500A) layers are strongly effected by imposed shear flow. This has important implications for our understanding of lubrication.. 

Figure (left) showing neutron reflection data from the mica water interface. The 'double critical edge' in the D2O sample is a characteristic of this interface. 

Adsorption to minerals

We have recently succeeded in making neutron reflection measurements from the surface of mica. Mica is a key mineral in many surface studies as it is atomically flat and smooth and has very interesting surface charge behaviour. However, it is very difficult to study by the usual neutron reflection methods. Recently we have been able to perform these experiments by preparing a very thin supported mica substrate and have used this to probe surfactant adsorption as a representative example of the technique.We have recently been able to study other important minerals including silica and calcite. 

Figure illustrating neutron reflection from the calcite oil inteface with a schematic illustration of the adsorbed monolayer.

Orientation and deformation of Colloidal Particles

Many industrially useful materials are dispersions of tiny particles suspended in another medium, called a 'colloidal dispersion'. These particles may be rod or plate shaped; for example, pigments in inks and clay particles in paper coatings. The orientation of the particles can have a big effect on the flow behaviour of the material. We have been developing approaches that allow the orientation distribution of particle to be fully characterised. In addition, we have also developed synthetic approaches for novel shape changing particles. We are also interested in 'deformable' particles that can change shape under an external influence, like applied pressure. One of the projects currently available is to study assemblies of deformable particles, with particularly important applications in energy production.

We also have some interests looking as several aspects of supercapitors, used to store energy and impotant in capturing energy from renewable sources. In particular we have investigated the behaviour of ions in non-aqueous solutions using neutron total scattering and demonstrated that the ions go around in small clusters, rather than as separate ions.  We have use sum-frequency spectroscopy to identify how cations and anions are arrtarcted to and repelled from a surface that is charging/discharging and some novel new neutron reflection approaches to look at the structure of cations and anions at the surface of charged materials (like mica and graphene) where we can see several layers of ions. We have also prepared a semiconduction metal organic framework (MOF). This iron containing compound has well defined channels surrounded by aromatic rings which overlap to give conduction through the pi systems. 


Much of the work is at international facilities including: Institute Laue-Langevin, Grenoble, France, ISIS, Rutherford Appleton Laboratory, Oxon, UK, and ESRF, Grenoble, France and other world leading scattering facilities.

Centre for Environmental and Industrial Flows

My appointment is joint between the Department of Chemistry and the Centre for Environmental and Industrial Flows

Take a tour of the Clarke lab facilities


C–H…N hydrogen bonding in an overlayer of s-triazine physisorbed on a graphite surface
J Davidson, S Clarke, S Jenkins, F Gorrec
– Molecular Physics
Self-assembly and adsorption of cetyltrimethylammonium bromide and didodecyldimethylammonium bromide surfactants at the mica-water interface.
G Tsagkaropoulou, FJ Allen, SM Clarke, PJ Camp
– Soft matter
Characterisation of Short Time Marine Corroded Surfaces
J Poon, SM Collins, DC Madden, H Sonke, SM Clarke
– Journal of the Electrochemical Society
Adsorption of 4-n-Nonylphenol, Carvacrol, and Ethanol onto Iron Oxide from Nonaqueous Hydrocarbon Solvents
RM Alloway, J Mong, IW Jephson, MH Wood, MTL Casford, P Grice, SV Filip, IE Salama, C Durkan, SM Clarke
– Langmuir
Multiscale Approach Linking Self-Aggregation and Surface Interactions of Synthesized Foulants to Fouling Mitigation Strategies
DM Kaimaki, BT Haire, HP Ryan, G Jiménez-Serratos, RM Alloway, M Little, J Morrison, IE Salama, MJ Tillotson, BE Smith, SJ Moorhouse, TS Totton, M Hodges, SG Yeates, P Quayle, SM Clarke, EA Müller, C Durkan
– Energy & Fuels
Novel semiconducting iron–quinizarin metal–organic framework for application in supercapacitors*
S Agrawal, SM Clarke, IJ Vitorica-Yrezabal, C Liu, W Fang, PT Wood, D Wright
– Molecular Physics
New insights into the solid–liquid interface exploiting neutron reflectivity
RJL Welbourn, SM Clarke
– Current Opinion in Colloid and Interface Science
Potassium, Calcium, and Magnesium Bridging of AOT to Mica at Constant Ionic Strength.
FJ Allen, CL Truscott, P Gutfreund, RJL Welbourn, SM Clarke
– Langmuir : the ACS journal of surfaces and colloids
Competitive Adsorption of a Multifunctional Amine and Phenol Surfactant with Ethanol on Hematite from Nonaqueous Solution
C-L Chia, RM Alloway, I Jephson, SM Clarke, SV Filip, FR Siperstein, C Avendaño
– The Journal of Physical Chemistry B
Anionic surfactant induced desorption of a cationic surfactant from mica.
F Allen, C Truscott, R Welbourn, S Clarke
– Applied Clay Science
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Research Interest Group

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01223 336469

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