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CMP
Credit: Jack Hobhouse

Grey Christoforo

Postdoctoral Research Assistant

Research theme

  • Photovoltaics and nanoscience

Sub department

  • Condensed Matter Physics

Research groups

  • Advanced Functional Materials and Devices (AFMD) Group
  • Snaith group
grey.christoforo@physics.ox.ac.uk
Robert Hooke Building, room G24
  • About
  • Education
  • Publications

Improving performance of fully scalable, flexible transparent conductive films made from carbon nanotubes and ethylene-vinyl acetate

Energy Reports Elsevier 8:S11 (2022) 48-60

Authors:

Bernd K Sturdza, Andreas E Lauritzen, Suer Zhou, Andre J Bennett, Joshua Form, M Greyson Christoforo, Robert M Dalgliesh, Henry J Snaith, Moritz K Riede, Robin J Nicholas

Abstract:

We report process improvements for the fabrication of single-walled carbon nanotube ethylene-vinyl acetate transparent conductive films. CNT:EVA films demonstrate high resilience against folding and can replace the external dopant in a spiro-OMeTAD based hole selective contact of n-i-p perovskite solar cells achieving a steady-state efficiency of 16.3%. The adapted process is fully scalable, and compared to previous reports (Mazzotta et al., 2018) lowers the material cost dramatically and improves DC to optical conductivity ratio by two orders of magnitude to σdc/σop = 3.6 for pristine and σdc/σop = 15 for chemically doped films. We analyse the microstructure of our films via small angle neutron scattering and find a positive correlation between the long range packing density of the CNT:EVA films and the σdc/σop performance. Increasing monomer ratio and chain length of the EVA polymer improves resilience against bending strain, whereas no significant effect on the CNT wrapping and electrical conductivity of resulting films is found.
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Visualizing macroscopic inhomogeneities in perovskite solar cells

University of Oxford (2022)

Authors:

Akash Dasgupta, Suhas Mahesh, Pietro Caprioglio, Yen-Hung Lin, Karl-Augustin Zaininger, Robert DJ Oliver, Philippe Holzhey, Suer Zhou, Melissa McCarthy, Joel Smith, Maximilian Frenzel, M Greyson Christoforo, James Ball, Bernard Wenger, Henry J Snaith

Abstract:

This contains all data used in the paper: ACS Energy Lett. 2022, 7, 7, 2311–2322, DOI: https://doi.org/10.1021/acsenergylett.2c01094. Data has been sorted into raw and processed, and organised by which figure they appear in. Arrays require Python and the numpy package to load (np.load('filename.npy')). All other data is in text format of some form, easily openable. Some plots require Origin labs to open, but no data in these files are inaccessible from the txt files/ csvs etc.
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Low-cost dopant-free carbazole enamine hole-transporting materials for thermally stable perovskite solar cells

Solar RRL Wiley 6:11 (2021) 2100984

Authors:

Suer Zhou, Maryte Daskeviciene, Matas Steponaitis, Giedre Bubniene, Vygintas Jankauskas, Kelly Schutt, Philippe Holzhey, Ashley R Marshall, Pietro Caprioglio, Grey Christoforo, James M Ball, Tadas Malinauskas, Vytautas Getautis, Henry J Snaith

Abstract:

Perovskite solar cells deliver high efficiencies, but are often made from high-cost bespoke chemicals, such as the archetypical hole-conductor, 2,2′,7,7′-tetrakis(N,N-di-p-methoxy-phenylamine)-9-9′-spirobifluorene (spiro-OMeTAD). Herein, new charge-transporting carbazole-based enamine molecules are reported. The new hole conductors do not require chemical oxidation to reach high power conversion efficiencies (PCEs) when employed in n-type-intrinsic-p-type perovskite solar cells; thus, reducing the risk of moisture degrading the perovskite layer through the hydrophilicity of oxidizing additives that are typically used with conventional hole conductors. Devices made with these new undoped carbazole-based enamines achieve comparable PCEs to those employing doped spiro-OMeTAD, and greatly enhanced stability under 85 °C thermal aging; maintaining 83% of their peak efficiency after 1000 h, compared with spiro-OMeTAD-based devices that degrade to 26% of the peak PCE within 24 h. Furthermore, the carbazole-based enamines can be synthesized without the use of organometallic catalysts and complicated purification techniques, lowering the material cost by one order of magnitude compared with spiro-OMeTAD. As a result, we calculate that the overall manufacturing costs of future photovoltaic (PV) modules are reduced, making the levelized cost of electricity competitive with silicon PV modules.
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Development of a beam imaging system for the European spallation source tuning dump

Nuclear Instruments and Methods in Physics Research Section A Accelerators Spectrometers Detectors and Associated Equipment Elsevier 950 (2020) 162790

Authors:

MG Ibison, CP Welsch, E Adli, H Gjersdal, G Christoforo, T Shea, C Thomas, D Naeem
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Solubilization of carbon nanotubes with ethylene-vinyl acetate for solution-processed conductive films and charge extraction layers in perovskite solar cells

ACS Applied Materials and Interfaces American Chemical Society 11:1 (2018) 1185-1191

Authors:

Giulio Mazzotta, Markus Dollmann, Habisreutinger, Greyson Christoforo, Zhiping Wang, Henry Snaith, Moritz Riede, Robin Nicholas

Abstract:

Carbon nanotube (CNT) solubilization via non-covalent wrapping of conjugated semiconducting polymers is a common technique used to produce stable dispersions for depositing CNTs from solution. Here, we report the use of a non-conjugated insulating polymer, ethylene vinyl acetate (EVA), to disperse multi- and single-walled CNTs (MWCNT and SWCNT) in organic solvents. We demonstrate that despite the insulating nature of the EVA, we can produce semitransparent films with conductivities of up to 34 S/cm. We show, using photoluminescence spectroscopy, that the EVA strongly binds to individual CNTs, thus making them soluble, preventing aggregation, and facilitating the deposition of high-quality films. To prove the good electronic properties of this composite, we have fabricated perovskite solar cells using EVA/SWCNTs and EVA/MWCNTs as selective hole contact, obtaining power conversion efficiencies of up to 17.1%, demonstrating that the insulating polymer does not prevent the charge transfer from the active material to the CNTs.
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