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CMP
Credit: Jack Hobhouse

Dr Pascal Kaienburg

Postdoctoral Research Fellow

Sub department

  • Condensed Matter Physics

Research groups

  • Advanced Functional Materials and Devices (AFMD) Group
pascal.kaienburg@physics.ox.ac.uk
Telephone: 01865282330
Robert Hooke Building, room G29
  • About
  • Publications

Spin-coated planar Sb2S3 hybrid solar cells approaching 5% efficiency

Beilstein Journal of Nanotechnology Beilstein Institut 9:1 (2018) 2114-2124

Authors:

Pascal Kaienburg, Benjamin Klingebiel, Thomas Kirchartz
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Developing design criteria for organic solar cells using well-absorbing non-fullerene acceptors

Communications Physics Springer Nature 1:1 (2018) 27

Authors:

Lisa Krückemeier, Pascal Kaienburg, Jan Flohre, Karsten Bittkau, Irene Zonno, Benedikt Krogmeier, Thomas Kirchartz
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Understanding Thermal Admittance Spectroscopy in Low-Mobility Semiconductors

JOURNAL OF PHYSICAL CHEMISTRY C 122:18 (2018) 9795-9803

Authors:

Shuo Wang, Pascal Kaienburg, Benjamin Klingebiel, Diana Schillings, Thomas Kirchartz
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Figures of Merit Guiding Research on Organic Solar Cells

JOURNAL OF PHYSICAL CHEMISTRY C 122:11 (2018) 5829-5843

Authors:

Thomas Kirchartz, Pascal Kaienburg, Derya Baran
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Reduced voltage losses yield 10% efficient fullerene free organic solar cells with >1 V open circuit voltages

Energy and Environmental Science Royal Society of Chemistry 9:12 (2016) 3783-3793

Authors:

D Baran, T Kirchartz, Scot Wheeler, S Dimitrov, M Abdelsamie, J Gorman, RS Ashraf, S Holliday, A Wadsworth, N Gasparini, P Kaienburg, H Yan, A Amassian, CJ Brabec, I McCulloch

Abstract:

Optimization of the energy levels at the donor–acceptor interface of organic solar cells has driven their efficiencies to above 10%. However, further improvements towards efficiencies comparable with inorganic solar cells remain challenging because of high recombination losses, which empirically limit the open-circuit voltage (Voc) to typically less than 1 V. Here we show that this empirical limit can be overcome using non-fullerene acceptors blended with the low band gap polymer PffBT4T-2DT leading to efficiencies approaching 10% (9.95%). We achieve Voc up to 1.12 V, which corresponds to a loss of only Eg/q − Voc = 0.5 ± 0.01 V between the optical bandgap Eg of the polymer and Voc. This high Voc is shown to be associated with the achievement of remarkably low non-geminate and non-radiative recombination losses in these devices. Suppression of non-radiative recombination implies high external electroluminescence quantum efficiencies which are orders of magnitude higher than those of equivalent devices employing fullerene acceptors. Using the balance between reduced recombination losses and good photocurrent generation efficiencies achieved experimentally as a baseline for simulations of the efficiency potential of organic solar cells, we estimate that efficiencies of up to 20% are achievable if band gaps and fill factors are further optimized.

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