The deposition and optoelectronic properties of reduced graphene oxide thin films are described. Thin films with thicknesses ranging from 1-10 nm have been deposited by the vacuum filtration method. The conductivity of the thin films can be varied over six orders of magnitude by varying the filtration volume of the graphene oxide aqueous suspension while maintaining the transmittance between 60%-95%. In addition, enhancement in the conductance through Cl doping is demonstrated. The combination of the reduction and Cl treatments make the reduced graphene oxide thin films sufficiently conducting to incorporate them as the hole collecting electrode in proof of concept organic photovoltaic devices.

Improvement of the photovoltaic efficiency via exposure of organic poly(3-hexylthiophene) (P3HT) and phenyl-C 61 -butyric acid methyl ester (PCBM) devices to solvent vapor at room temperature is reported. In situ photoluminescence (PL) and Raman spectroscopy, in conjunction with ex situ optical absorption and atomic force microscopy, have been used to provide insight into the nanoscale morphological changes occurring during solvent vapor annealing. We found that in 1 : 1 composites of P3HT : PCBM, suppression of PL, narrowing in line-width of the 1442 cm 21 P3HT Raman peak, and strong modifications in the optical absorption spectra were observed during solvent vapor annealing, while minimal changes occurred in pure P3HT films. We attribute these spectral modifications to de-mixing of PCBM and subsequent stacking of P3HT in coplanar conjugated segments, similar to what is observed during thermal annealing.

Scheme 1 a a Conditions: (a) synthesis scheme of R-vinyl-ω-(phenyl) end-functionalized P3HT; (b) R-vinyl-ω-(phenyl) end-functionalized P3HT is activated by s-BuLi and forms 3, which subsequently serves as an anionic macroinitiator for the synthesis of P3HT-P2VP; dppp ) propane-1,3-diylbis-(diphenylphosphane).

Solution processable planar heterojunction perovskite solar cell is a very promising new technology for low cost renewable energy. One of the most common cell structures is FTO/TiO2/CH3NH3PbI3-xClx/spiro-OMeTAD/Au. The main issues of this type of solar cell are the poor coverage and morphology control of the perovskite CH3NH3PbI3-xClx film on TiO2. For the first time, we demonstrate that the problems can be easily resolved by using a polymer additive in perovskite precursor solution during the film formation process. A 25% increase in power conversion efficiency at a value of 13.2% is achieved by adding 1 wt % of poly(ethylene glycol) in the perovskite layer using a 150 °C processed TiO2 nanoparticle layer. The morphology of this new perovskite was carefully studied by SEM, XRD, and AFM. The results reveal that the additive controls the size and aggregation of perovskite crystals and helps the formation of smooth film over TiO2 completely. Thus, the Voc and Jsc are greatly increased for a high efficiency solar cell. The amount of additive is optimized at 1 wt % due to its insulating characteristics. This research provides a facile way to fabricate a high efficiency perovskite solar cell by the low temperature solution process (<150 °C), which has the advancement of conserving energy over the traditional high temperature sintering TiO2 compact layer device.

CdSe quantum dots have been encapped with aromatic ligands: a-toluenethiol, thiophenol, and p-hydroxythiophenol to enhance the photoluminescence (PL) quenching and photoelectric properties of the quantum dots. The aromatic ligand capped CdSe quantum dots are prepared through ligand exchange with trioctylphosphine oxide (TOPO) capped CdSe quantum dots. The XPS surface chemistry analysis and elemental analysis has confirmed the success of ligand exchange from TOPO to aromatic ligands. Both XRD and HRTEM-SAED studies indicate the crystalline structure of CdSe quantum dots not only remains but is also improved by the ligand exchange of TOPO with thiol molecules. Time resolved PL decay measurements indicate thiophenol and p-hydroxythiophenol ligands effectively quench the emission and have much shorter PL lifetimes than that of TOPO and that of a-toluenethiol. Thus, both thiophenol and p-hydroxythiophenol can act as an effective acceptor for photogenerated holes through aromatic p-electrons. Thiophenol also exhibits good charge transport behavior showing a 10-fold increase in short circuit current density (I sc ) as compared with TOPO in the photocurrent study of fabricated photovoltaic devices.