Imperial College London

MrCharlieHenderson

Faculty of Natural SciencesDepartment of Physics

Research Postgraduate
 
 
 
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Contact

 

c.henderson21

 
 
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Location

 

724Huxley BuildingSouth Kensington Campus

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Summary

 

Publications

Publication Type
Year
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3 results found

Henderson C, Luke J, Bicalho I, Correa L, Yang E, Rimmele M, Demetriou H, Heutz S, Gasparini N, Heeney M, Bagnis D, Kim JSet al., 2023, Charge transfer complex formation between organic interlayers drives light-soaking in large area perovskite solar cells, Energy and Environmental Science, Vol: 16, Pages: 5891-5903, ISSN: 1754-5692

Light soaking (LS) is a well-known but poorly understood phenomenon in perovskite solar cells (PSCs) which significantly affects device efficiency and stability. LS is greatly reduced in large-area inverted PSCs when a PC61BM electron transport layer (ETL) is replaced with C60, where the ETL is commonly in contact with a thin bathocuproine (BCP) interlayer. Herein, we identify the key molecular origins of this LS effect using a combination of surface photovoltage, ambient photoemission spectroscopy, Raman spectroscopy, integrated with density functional theory simulations. We find that BCP forms a photoinduced charge-transfer (CT) complex with both C60 and PC61BM. The C60/BCP complex accelerates C60 dimer formation, leading to a favourable cascading energetic landscape for electron extraction and reduced recombination loss. In contrast, the PC61BM/BCP complex suppresses PC61BM dimer formation, meaning that PC61BM dimerisation is not the cause of LS. Instead, it is the slow light-induced formation of the PC61BM/BCP CT complex itself, and the new energetic transport levels associated with it, which cause the much slower and stronger LS effect of PC61BM based PSCs. These findings provide key understanding of photoinduced ETL/BCP interactions and their impact on the LS effect in PSCs.

Journal article

Bellchambers P, Henderson C, Abrahamczyk S, Choi S, Lee J, Hatton RAet al., 2023, High Performance Transparent Silver Grid Electrodes for Organic Photovoltaics Fabricated by Selective Metal Condensation, Advanced Materials, Vol: 35, ISSN: 0935-9648

<jats:title>Abstract</jats:title><jats:p>Silver grid electrodes on glass and flexible plastic substrates with performance that exceeds that of commercial indium‐tin oxide (ITO) coated glass are reported and show their suitability as a drop‐in replacement for ITO glass in solution‐processed organic photovoltaics (OPVs). When supported on flexible plastic substrates these electrodes are stable toward repeated bending through a small radius of curvature over tens of thousands of cycles. The grid electrodes are fabricated by the unconventional approach of condensation coefficient modulation using a perfluorinated polymer shown to be far superior to the other compounds used for this purpose to date. The very narrow line width and small grid pitch that can be achieved also open the door to the possibility of using grid electrodes in OPVs without a conducting poly(3,4‐ethylenedioxythiophene‐poly(styrenesulfonate) (PEDOT: PSS) layer to span the gaps between grid lines.</jats:p>

Journal article

Chin Y-C, Daboczi M, Henderson C, Luke J, Kim J-Set al., 2022, Suppressing PEDOT:PSS doping-induced interfacial recombination loss in perovskite solar cells, ACS Energy Letters, Vol: 7, Pages: 560-568, ISSN: 2380-8195

PEDOT:PSS is widely used as a hole transport layer (HTL) in perovskite solar cells (PSCs) due to its facile processability, industrial scalability, and commercialization potential. However, PSCs utilizing PEDOT:PSS suffer from strong recombination losses compared to other organic HTLs. This results in lower open-circuit voltage (VOC) and power conversion efficiency (PCE). Most studies focus on doping PEDOT:PSS to improve charge extraction, but it has been suggested that a high doping level can cause strong recombination losses. Herein, we systematically dedope PEDOT:PSS with aqueous NaOH, raising its Fermi level by up to 500 meV, and optimize its layer thickness in p-i-n devices. A significant reduction of recombination losses at the dedoped PEDOT:PSS/perovskite interface is evidenced by a longer photoluminescence lifetime and higher magnitude of surface photovoltage, leading to an increased device VOC, fill factor, and PCE. These results provide insights into the relationship between doping level of HTLs and interfacial charge carrier recombination losses.

Journal article

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