Home  >>  Characterisation  >>  XPS
new characterisation

XPS

Our x-ray photoelectron spectrometer (XPS) facility is ideal for material analysis under variable environmental conditions.

Key features:

  • CORDE offers three XPS instruments with a wide range of capabilities and fast throughput of standard XPS measurements
  • We can tailor experiments for specific requirements and provide professional support with high quality data acquisition and analysis
  • Can be applied to a broad range of materials and provides valuable quantitative and chemical state information from the surface of material being studied.
  • Supports a variety of industrial and research applications where surface plays a critical role in performance including: nanomaterials, photovoltaics, catalysis, corrosion, adhesion, electronic devices and packaging, magnetic media, display technology, batteries, surface treatments, and thin film coatings used for numerous applications.

Our Instruments

A multi-technique instrument with flexibility and configurability.

For high-throughput chemical surface analysis under application-relevant environmental conditions.

A high-performance X-ray photoelectron spectrometer with fast sample loading.

Operating Modes

User Mode

Service Mode

Enquire about this Facility

If you are new to CORDE we would recommend contacting us via the form below to ensure we can help you with a detailed response. Or you can contact the XPS Facility Scientist directly at xps@phy.cam.ac.uk.

Selected Publications

Zulqurnain, M., Burton, O., Al-Hada, M., Goff, L., Hofmann, S., & Hirst, L. C.

Defect seeded remote epitaxy of GaAs films on graphene

in: Nanotechnology, 33, 485603. (2022). doi: 10.1088/1361-6528/ac8a4f

Remote epitaxy is an emerging materials synthesis technique which employs a 2D interface layer, often graphene, to enable the epitaxial deposition of low defect single crystal films while restricting bonding between the growth layer and the underlying substrate. This allows for the subsequent release of the epitaxial film for integration with other systems and reuse of growth substrates. This approach is applicable to material systems with an ionic component to their bonding, making it notably appealing for III–V alloys, which are a technologically important family of materials. Chemical vapour deposition growth of graphene and wet transfer to a III–V substrate with a polymer handle is a potentially scalable and low cost approach to producing the required growth surface for remote epitaxy of these materials, however, the presence of water promotes the formation of a III–V oxide layer, which degrades the quality of subsequently grown epitaxial films. This work demonstrates the use of an argon ion beam for the controlled introduction of defects in a monolayer graphene interface layer to enable the growth of a single crystal GaAs film by molecular beam epitaxy, despite the presence of a native oxide at the substrate/graphene interface. A hybrid mechanism of defect seeded lateral overgrowth with remote epitaxy contributing the coalescence of the film is indicated. The exfoliation of the GaAs films reveals the presence of defect seeded nucleation sites, highlighting the need to balance the benefits of defect seeding on crystal quality against the requirement for subsequent exfoliation of the film, for future large area development of this approach.

Ian E. Jacobs, Gabriele D’Avino, Vincent Lemaur, Yue Lin, Yuxuan Huang, Chen Chen, Thomas F. Harrelson, William Wood, Leszek J. Spalek, Tarig Mustafa, Christopher A. O’Keefe, Xinglong Ren, Dimitrios Simatos, Dion Tjhe, Martin Statz, Joseph W. Strzalka, Jin-Kyun Lee, Iain McCulloch, Simone Fratini, David Beljonne, and Henning Sirringhaus

Structural and Dynamic Disorder, Not Ionic Trapping, Controls Charge Transport in Highly Doped Conducting Polymers

in: Journal of the American Chemical Society  144 (7), 3005-3019 (2022). doi: 10.1021/jacs.1c10651

Doped organic semiconductors are critical to emerging device applications, including thermoelectrics, bioelectronics, and neuromorphic computing devices. It is commonly assumed that low conductivities in these materials result primarily from charge trapping by the Coulomb potentials of the dopant counterions. Here, we present a combined experimental and theoretical study rebutting this belief. Using a newly developed doping technique based on ion exchange, we prepare highly doped films with several counterions of varying size and shape and characterize their carrier density, electrical conductivity, and paracrystalline disorder. In this uniquely large data set composed of several classes of high-mobility conjugated polymers, each doped with at least five different ions, we find electrical conductivity to be strongly correlated with paracrystalline disorder but poorly correlated with ionic size, suggesting that Coulomb traps do not limit transport. A general model for interacting electrons in highly doped polymers is proposed and carefully parametrized against atomistic calculations, enabling the calculation of electrical conductivity within the framework of transient localization theory. Theoretical calculations are in excellent agreement with experimental data, providing insights into the disorder-limited nature of charge transport and suggesting new strategies to further improve conductivities.