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Issue 5, 2016
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Highly efficient organic photovoltaic devices utilizing work-function tuned graphene oxide derivatives as the anode and cathode charge extraction layers

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Abstract

The effective utilization of work-function (WF) tuned solution processable graphene-based derivatives as both hole and electron transport layers in organic photovoltaic (OPV) devices is demonstrated. The systematic tuning of the functionalized graphene oxide (GO) WF took place by either photochlorination for WF increase, or lithium neutralization for WF decrease. In this way, the WF of the photochlorinated GO layer was perfectly matched with the HOMO level of two different polymer donors, enabling excellent hole transport. Meanwhile the WF of the lithium functionalized GO was perfectly matched with the LUMO level of the fullerene acceptor, enabling excellent electron transport. The utilization of these graphene-based hole and electron transport layers in PTB7:PC71BM active layer devices led to ∼19% enhancement in the power conversion efficiency (PCE) compared to that of the reference graphene free device, resulting in the highest reported PCE for graphene-based buffer layer OPVs of 9.14%. The proposed techniques open new paths towards novel material and interface engineering approaches for a wide range of new applications, including flexible electronic devices, OPVs, perovskite solar cells, organic light emitting diodes, and photosensors, as well as traditional electronic devices.

Graphical abstract: Highly efficient organic photovoltaic devices utilizing work-function tuned graphene oxide derivatives as the anode and cathode charge extraction layers

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Publication details

The article was received on 29 Nov 2015, accepted on 22 Dec 2015 and first published on 22 Dec 2015


Article type: Communication
DOI: 10.1039/C5TA09712F
Citation: J. Mater. Chem. A, 2016,4, 1612-1623
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    Highly efficient organic photovoltaic devices utilizing work-function tuned graphene oxide derivatives as the anode and cathode charge extraction layers

    D. Konios, G. Kakavelakis, C. Petridis, K. Savva, E. Stratakis and E. Kymakis, J. Mater. Chem. A, 2016, 4, 1612
    DOI: 10.1039/C5TA09712F

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