Plasmon-active silver nanoparticle layers were included in solution-processed bulk-heterojunction solar cells. Nanoparticle layers were fabricated using vapor-phase deposition on indium tin oxide electrodes. Owing to the increase in optical electrical field inside the photoactive layer, the inclusion of such particle films lead to increased optical absorption and consequently increased photoconversion at solar-conversion relevant wavelengths. The resulting solar energy conversion efficiency for a bulk heterojunction photovoltaic device of poly(3-hexylthiophene)/[6,6]-phenyl C61 butyric acid methyl ester was found to increase from 1.3%±0.2% to 2.2%±0.1% for devices employing thin plasmon-active layers. Based on six measurements, the improvement factor of 1.7 was demonstrated to be statistically significant.

Adhesive forces measured with an atomic force microscope under ambient conditions are generally regarded to be dominated by non-surface-specific capillary force. In this study, the nature of the "pull-off" force on a variety of surfaces was investigated as a function of relative humidity. The results indicate that even under the condition where capillary condensation occurs there is chemical specificity in the measured pull-off force. Issues such as tip-surface contact time and surface roughness were ruled out as possible artifacts. A mathematical model of pull-off force as a function of relative humidity is proposed in which the chemical specificity is explained.

No abstract

Clinical and field-portable diagnostic devices require the detection of atto-to zeptomoles of biological molecules rapidly, easily and at low cost, with stringent requirements in terms of robustness and reliability. Though a number of creative approaches to this difficult problem have been reported 1-9 , numerous unmet needs remain in the marketplace, particularly in resource-poor settings [10][11][12] . Using rational materials design, we investigated harnessing the amplification inherent in a radical chain polymerization reaction to detect molecular recognition. Polymerization-based amplification is shown to yield a macroscopically observable polymer, easily visible to the unaided eye, as a result of as few as ~1,000 recognition events (10 zeptomoles). Design and synthesis of a dual-functional macromolecule that is capable both of selective recognition and of initiating a polymerization reaction was central to obtaining high sensitivity and eliminating the need for any detection equipment. Herein, we detail the design criteria that were used and compare our findings with those obtained using enzymatic amplification. Most excitingly, this new approach is general in that it is readily adaptable to facile detection at very low levels of specific biological interactions of any kind.