ABSTRACT
Reduced graphene oxide (rGO) has emerged as an excellent interfacial material for improvising the performance of dye-sensitized solar cells (DSSC). Herein, we have applied rGO as interfacial layers between a fluorine doped tin oxide (FTO) coated glass substrate and semiconducting material TiO2 in a photoanode of a DSSC which showed an unusual enhancement in generating a photocurrent in comparison to the control (without rGO layers). An electrochemical impedance spectroscopy (EIS) study was performed to gain the mechanistic insights into such a remarkable enhancement of photoelectric conversion efficiency (PCE) which revealed improved charge transfer and suppressed charge recombination due to high-electrical conductivity and probably more negative work function of our rGO material compared to the bare TiO2 photoanode.
ABSTRACT
Downsizing coordination polymers (CPs) to thin film configurations is a prerequisite for device applications. However, fabrication of thin films of CPs including metal-organic frameworks (MOFs) with reasonable electrical conductivity is challenging. Herein, thin film fabrication of a Cu(ii)-CP employing a layer-by-layer method is demonstrated whereby a self-assembled monolayer on Au was used as the functionalized substrate. Growth of the Cu(ii)-CP at the solid-liquid interface generated open-metal Cu(ii) sites in the thin film which were susceptible to activation by molecular dopant molecules. A significant enhancement in in-plane electrical conductivity and an unheralded cross-plane current rectification ratio (exceeding 105 both at room-temperature and at an elevated temperature) were achieved. Such a remarkable rectification ratio was realized, similar to those of commercial Si rectifier diodes. This phenomenon is attributed to the formation of an electronic heterostructure in the molecularly doped thin film. Molecular doping additionally transformed the interfacial properties of thin films from hydrophilic to highly hydrophobic.
