Understanding the petal effect: Wetting properties and surface structure of natural rose petals and rose petal-derived surfaces.

The petal effect is identified as a non-wetting state with high drop adhesion. The wetting behavior of petal surfaces is attributed to the papillose structure of their epidermis, which leads to a Cassie-Baxter regime combined with strong pinning sites. Under this scenario, sessile drops are pearl shaped and, unlike lotus-like surfaces, firmly attached to the surface. Petal surfaces are used as inspiration for the fabrication of functional parahydrophobic surfaces such as antibacterial or water-harvesting surfaces. In this work, two types of rose petals were replicated by using a templating technique based in Polydimethylsiloxane (PDMS) nanocasting. The topographic structure, the condensation mechanism under saturated environments and the wetting properties of the natural rose petal and their negative and positive replicas were analyzed. Finally, we performed prospective ice adhesion studies to elucidate whether petal-like surfaces may be used as deicing solutions.

Making sense of agrobiodiversity, diet, and intensification of smallholder family farming in the Highland Andes of Ecuador.

Methods are needed for helping researchers and farmers to interactively describe and analyze local practices in search of opportunities for improving health, environment, and economy. The authors worked with smallholder family farmers in five Andean villages in Ecuador to apply participatory four-cell analysis (PFCA) in characterizing agrobiodiversity. Margelef and Shannon indices examined ecological richness and evenness, and a simplified 24-hour dietary recall characterized food consumption. Cross-analysis tested interactions among agrobiodiversity, farm size, and diet. Overall trends appeared to work against sustainable intensification, with notable heterogeneity and positive deviance found in the practices of relatively smaller enterprises, representing a potential resource for sustainable intensification. The suite of methods was determined useful for initiating researcher-farmer explorations of promising innovation pathways.

The use of nanocarbons as chemical filters for the selective detection of nitrogen dioxide and ozone.

The gas filtering abilities of different nanocarbon materials such as nanocones/nanodiscs, and nanofibres, either as-prepared or modified by physical (annealing, grinding) or chemical (fluorination) treatment are reported. The aptitude to filter nitrogen dioxide and ozone, two of the most significant gaseous pollutants of the atmosphere, have been correlated to both the BET specific surface area studied by N2 adsorption at 77 K, and the presence of chemical functional groups at the surface. Valuable information regarding the mechanisms of gas-nanocarbon interaction has been obtained, in terms of chemisorption and physisorption. A prototype microsystem is proposed for the selective measurement of nitrogen dioxide and ozone concentration by means of organic semiconductor gas sensors.

Molecular semiconductor-doped insulator (MSDI) heterojunctions: an alternative transducer for gas chemosensing.

New organic devices including a heterojunction between a semiconducting molecular material (MS)--lutetium bisphthalocyanine (LuPc2)--and a doped insulator (DI)--copper phthalocyanine (Cu(F(n)Pc), where n = 0, 8, 16)--are designed and studied as transducers for redox-active species sensing.

Grafting of porphyrins on cellulose nanometric films.

Ultrathin films of cellulose were functionalized with iron protoporphyrin IX (FePP). Spin-coating allows the production of silylated cellulose films in a controlled way. Cellulose regeneration is achieved through the hydrolyzation of the silane groups, exposing the film to acidic vapors. To enhance the reactivity of the cellulose surface to the protoporphyrin, carbonyldiimidazole (CDI) was used as an activator. The effect of different spacers on the porphyrin grafting such as 1,8-diaminooctane and 1,4-phenylenediamine was studied. The highest level of cellulose functionalization with FePP was achieved when both the cellulose film and FePP were activated by CDI and a diaminoalkane was used as a spacer between the surface and the FePP. ATR/MIR (attenuated total reflection in multiple internal reflections) was performed in situ to follow the kinetics of the different chemical reactions with the cellulose surface. ATR/MIR proved again to be a powerful tool for probing the surface reaction. X-ray photoelectron spectroscopy permitted the elemental analysis of the cellulose surface after the chemical modification.

Electroactivity of a starburst hole-transport material in Langmuir-Blodgett films. Solid state effects and intervalence charge transfer.

Here we report on the electroactivity properties of Langmuir-Blodgett (LB) films of the hole-transport molecule 4,4',4''-tris[3-methylphenyl(phenyl)amino] triphenylamine (m-MTDATA). Fairly stable Langmuir films at the air-water interface are accomplished, despite the non-amphiphilic character of the molecule. The reflection-absorption infrared spectroscopy (RAIRS) and Fourier transform infrared (FT-IR) analysis revealed that the molecules arrange with no neat preferential orientation, in agreement with the amorphous glassy nature of this starburst molecule. However, there is a tendency of the molecules to organize in a more planar conformation due to the intermolecular stacking induced by the LB technique. On the other hand, the fundamental electrochemistry (by cyclic voltammetry, CV) of the films is also analyzed. The CV studies of both solution and films reveal that both the solid state and the electrolyte's anions clearly affect the m-MTDATA's electroactivity, exhibiting a unique and broad redox process instead of the two reversible oxidations observed in solution. The oxidization mechanism is discussed. Finally, the spectroelectrochemistry studies evidence that the oxidization of the films leads to new absorption bands, among which the emerging bands in the NIR region ascribed to intervalence charge transfer (IVCT) between the generated aminyl radical cations should be pointed out.

New hybrid films based on cellulose and hydroxygallium phthalocyanine. Synergetic effects in the structure and properties.

Hydroxygallium phthalocyanine (HOGaPc) and cellulose (from a trimethylsilyl derivative) have been used as native elements for the preparation of a novel family of hybrid films. By spin-coating, both components allow the building of films with different configurations on various substrates in a controlled way. The particularities of these hybrid films have been characterized by a range of techniques such as Fourier transform infrared spectroscopy (FTIRS) in attenuated total reflection using multiple internal reflections (ATR/MIR), absorption ultraviolet and visible spectroscopy (UV-vis), X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and surface potential measurements using the Kelvin-Zisman vibrating capacitor probe (KP). This enabled determination of the influence of cellulose on the arrangement of HOGaPc and, consequently, control of the relation between the structure and the properties of the films. Finally, gas sensor tests were performed to check the potentialities of these hybrid films. In particular, the synergetic behavior between the film-forming materials allows a fast and sensible change in surface potential after cyclic exposures to ozone (O3, 100 ppb) and nitrogen. Overall, we present the advantages of combining phthalocyanine with cellulose in enhancing the properties of the final product. Introduction of cellulose as a host material opens up a new area of hybrid films.

A Novel Gas Sensor Transducer Based on Phthalocyanine Heterojunction Devices.

Experimental data concerning the changes in the current-voltage (I-V) perfor-mances of a molecular material-based heterojunction consisting of hexadecafluorinatednickel phthalocyanine (Ni(F16Pc)) and nickel phthalocyanine (NiPc),(Au|Ni(F16Pc)|NiPc|Al) are introduced as an unprecedented principle of transduction for gassensing performances. The respective n- and p-type doped-insulator behaviors of therespective materials are supported, owing to the observed changes in surface potential(using the Kelvin probe method) after submission to electron donor (ammonia) and electronacceptor gases (ozone). On the other hand, the bilayer device exhibits strong variations inthe built-in potential of the junction and in its rectification ratio. Moreover, large increasesoccur in forward and reverse currents in presence of ammonia vapors. These make possiblea multimodal principle of detection controlled by a combined effect between theheterojunction and the NiPc|Al contact. Indeed, this metal/organic junction plays a criticalrole regarding the steady asymmetry of the I-V profiles during the device's doping evenusing high ammonia concentrations. This approach offers a more sophisticated alternative tothe classically studied, but at times rather operation-limited, resistive gas sensors.