No abstract

Quantum dot-sensitized solar cells (QDSSCs) are interesting energy devices because of their (i) impressive ability to harvest sunlight and generate multiple electron/hole pairs, (ii) ease of fabrication, and (iii) low cost. The power conversion efficiencies (η) of most QDSSCs (typically <4%) are, however, less than those (up to 12%) of dye-sensitized solar cells, mainly because of narrow absorption ranges and charge recombination occurring at the QD-electrolyte and TiO(2)-electrolyte interfaces. To further increase the values of η of QDSSCs, it will be necessary to develop new types of working electrodes, sensitizers, counter electrodes and electrolytes. This Feature Article describes the nanomaterials that have been used recently as electronic conductors, sensitizers and counter electrodes in QDSSCs. The nature, size, morphology and quantity of these nanomaterials all play important roles affecting the efficiencies of electron injection and light harvesting. We discuss the behavior of several important types of semiconductor nanomaterials (sensitizers, including CdS, Ag(2)S, CdSe, CdTe, CdHgTe, InAs and PbS) and nanomaterials (notably TiO(2), ZnO and carbon-based species) that have been developed to improve the electron transport efficiency of QDSSCs. We point out the preparation of new generations of nanomaterials for QDSSCs and the types of electrolytes, particularly iodide/triiodide electrolytes (I(-)/I(3)(-)), polysulfide electrolytes (S(2-)/S(x)(2-)), and cobalt redox couples ([Co(o-phen)(3)(2+)/(3+)]), that improve their lifetimes. With advances in nanotechnology, we foresee significant improvements in the efficiency (η > 6%) and durability (>3000 h) of QDSSCs.

A simple hydrothermal method of preparing highly photocatalytic graphene-ZnO-Au nanocomposites (G-ZnO-Au NCs) has been developed. Zinc acetate and graphene oxide are reduced by catechin to form graphene-zinc oxide nanospheres (G-ZnO NSs; average diameter of (45.3 ± 3.7) nm) in the presence of ethylenediamine (EDA) as a stabilizing agent and gold nanorods (Au NRs) at 300 °C for 2 h. Then Au NRs are deposited onto as-formed G-ZnO NSs to form G-ZnO-Au NCs. Upon ultraviolet light activation, G-ZnO-Au NCs (4 mg mL(-1)) in methanol generates electron-hole pairs. Methanol (hydroxyl group) assists in trapping holes, enabling photogenerated electrons to catalyze reduction of nitrobenzene (NB) to aniline with a yield of 97.8% during a reaction course of 140 min. The efficiency of G-ZnO-Au NCs is 3.5- and 4.5-fold higher than those provided by commercial TiO2 and ZnO NSs, respectively. Surface assisted laser desorption/ionization mass spectrometry has been for the first time applied to detect the intermediates (nitrosobenzene and phenylhydroxylamine) and major product (aniline) of NB through photoelectrocatalytic or photocatalytic reactions. The result reveals that the reduction of NB to aniline is through nitrosobenzene to phenylhydroxylamine in the photoelectrocatalytic reaction, while via nitrosobenzene directly in the photocatalytic reaction. G-ZnO-Au NC photocatalyst holds great potential in removal of organic pollutants like NB and in the production of aniline.

Hybrid quantum dot-graphene photodetectors have recently attracted substantial interest because of their remarkable performance and low power consumption. However, the performance of the device greatly depends on the interfacial states and photogenerated screening fi eld. As a consequence, the sensitivity is limited and the response time is relatively slow. In order to circumvent these challenges, herein, a composite graphene and graphene quantum dot (GQD) photodetector on lead zirconate titanate (Pb(Zr 0.2 Ti 0.8 )O 3 ) (PZT) substrates has been designed to form an ultrasensitive photodetector over a wide range of illumination power. Under 325 nm UV light illumination, the device shows sensitivity as high as 4.06 × 10 9 A W −1 , which is 120 times higher than reported sensitivity of the same class of devices. Plant derived GQD has a broad range of absorptivity and is an excellent candidate for harvesting photons generating electron-hole pairs. Intrinsic electric fi eld from PZT substrate separates photogenerated electron-hole pairs as well as provides the built-in electric fi eld that causes the holes to transfer to the underlying graphene channel. The composite structure of graphene and GQD on PZT substrate therefore produces a simple, stable, and highly sensitive photodetector over a wide range of power with short response time, which shows a way to obtain high-performance optoelectronic devices.

Graphene quantum dots (GQDs) have been prepared for the first time using raw plant leaf extracts of Neem (Azadirachta indica) and Fenugreek (Trigonella foenum-graecum) by a facile, hydrothermal method at 300 1C for 8 hours in water, without the need of any passivizing, reducing agents or organic solvents. High resolution transmission electron microscope studies showed that the average sizes of the GQDs from Neem (N-GQDs) and Fenugreek (F-GQDs) were 5 and 7 nm respectively. N-GQDs and F-GQDs exhibit high quantum yields of 41.2% and 38.9% respectively. Moreover, the GQDs were utilized to prepare a white light converting cap based on the red-green-blue (RGB) color mixing method.