Beneficial Role of Reduced Graphene Oxide for Electron Extraction in Highly Efficient Perovskite Solar Cells.

In this work we systematically investigated the role of reduced graphene oxide (rGO) in hybrid perovskite solar cells (PSCs). By mixing rGO within the mesoporous TiO2 (m-TiO2 ) matrix, highly efficient solar cells with power conversion efficiency values up to 19.54 % were realized. In addition, the boosted beneficial role of rGO with and without Li-treated m-TiO2 is highlighted, improving transport and injection of photoexcited electrons. This combined system may pave the way for further development and optimization of electron transport and collection in high efficiency PSCs.

Solution processed reduced graphene oxide electrodes for organic photovoltaics.

Since the isolation of free standing graphene in 2004, graphene research has experienced a phenomenal growth. Due to its exceptional electronic, optical and mechanical properties, graphene is believed to be the next wonder material for optoelectronics. The enhanced electrical conductivity, combined with its high transparency in the visible and near-infrared regions of the spectrum, enabled graphene to be an ideal low cost indium-tin oxide (ITO) substitute. Solution-processed reduced graphene oxide combines the unique optoelectrical properties of graphene with large area deposition and flexible substrates rendering it compatible with roll-to-roll manufacturing methods. This paper provides an overview of recent research progress in the application and consequent physical-chemical properties of solution-processed reduced graphene oxide-based films as transparent conductive electrodes (TCEs) in organic photovoltaic (OPV) cells. Reduced graphene oxide (rGO) can be effectively utilized as the TCE in flexible OPVs, where the brittle and expensive ITO is incompatible. The prospects and future research trends in graphene-based TCEs are also discussed.

Dispersion behaviour of graphene oxide and reduced graphene oxide.

The dispersion behaviour of graphene oxide (GO) and chemically reduced GO (rGO) has been investigated in a wide range of organic solvents. The effect of the reduction process on the GO solubility in eighteen different solvents was examined and analysed, taking into consideration the solvent polarity, the surface tension and the Hansen and Hildebrand solubility parameters. rGO concentrations up to ∼9 µg/mL in chlorinated solvents were achieved, demonstrating an efficient solubilization strategy, extending the scope for scalable liquid-phase processing of conductive rGO inks for the development of printed flexible electronics.

Improving the efficiency of organic photovoltaics by tuning the work function of graphene oxide hole transporting layers.

A facile, fast, non-destructive and roll-to-roll compatible photochemical method for simultaneous partial reduction and doping of graphene oxide (GO) films through ultraviolet laser irradiation in the presence of a Cl2 precursor gas is demonstrated. The photochemical chlorinated GO-Cl films were fully characterized by XPS and Raman measurements, in which grafting of chloride to the edges and the basal plane of GO was confirmed. By tuning the laser exposure time, it is possible to control the doping and reduction levels and therefore to tailor the work function (WF) of the GO-Cl layers from 4.9 eV to a maximum value of 5.23 eV. These WF values match with the HOMO level of most polymer donors employed in OPV devices. Furthermore, high efficiency poly(2,7-carbazole) derivative (PCDTBT):fullerene derivative (PC71BM) based OPVs with GO-Cl as the hole transporting layer (HTL) were demonstrated with a power conversion efficiency (PCE) of 6.56% which is 17.35% and 19.48% higher than that of the pristine GO and PEDOT:PSS based OPV devices, respectively. The performance enhancement was attributed to more efficient hole transportation due to the energy level matching between the GO-Cl and the polymer donor.