Time-course trend and influencing factors for per- and polyfluoroalkyl substances in the breast milk of Korean mothers.

Many studies have reported that neonates and infants are exposed to several per- and polyfluoroalkyl substances (PFASs) via breastfeeding; however, these studies have had small sample sizes. This study aimed to determine the concentrations and time-course trend of PFASs in breast milk and identify influencing factors governing PFAS concentrations. Between July and September (2018), 207 low-risk primiparous women were recruited from a lactation counseling clinic in Korea and their breast milk samples were tested for 14 PFASs, including four perfluoroalkyl sulfonic acids. A questionnaire survey, comprising 84 questions covering the women's demographic, obstetrical, dietary, lifestyle, behavioral, and neonatal information, was conducted to investigate associations. Twelve of the 14 PFASs were detectable in breast milk samples. Perfluorooctanesulfonic acid (PFOS), perfluorooctanoic acid (PFOA), and perfluorodecanoic acid were detected in 100% of the samples, followed by perfluorohexanesulfonic acid (detection rate: 87%), perfluorononanoic acid (87%), and perfluorohexanoic acid (73%); the median concentrations were 0.05, 0.10, 0.031, 0.007, and 0.033 ng/mL, respectively. The PFAS concentrations in breast milk measured in our study were higher than those reported in other studies or countries. In 12 years, from 2007 to 18, the mean concentration of PFOA in breast milk increased by approximately three times (278%). The major factors associated with PFAS concentrations in the bivariate association analysis were body mass index; living area (non-metropolitan); neonatal age; and frequency of fish, ice cream, and canned food consumption. In the multiple regression model, fish consumption significantly influenced the PFOS concentrations in breast milk (ß = 0.88, p = 0.033). Frequently, fish consumption has been analyzed as the main dietary factor related to PFOS concentration. Our findings suggest the need for a comprehensive cohort study on PFAS exposure and its association with infant health.

Soft network composite materials with deterministic and bio-inspired designs.

Hard and soft structural composites found in biology provide inspiration for the design of advanced synthetic materials. Many examples of bio-inspired hard materials can be found in the literature; far less attention has been devoted to soft systems. Here we introduce deterministic routes to low-modulus thin film materials with stress/strain responses that can be tailored precisely to match the non-linear properties of biological tissues, with application opportunities that range from soft biomedical devices to constructs for tissue engineering. The approach combines a low-modulus matrix with an open, stretchable network as a structural reinforcement that can yield classes of composites with a wide range of desired mechanical responses, including anisotropic, spatially heterogeneous, hierarchical and self-similar designs. Demonstrative application examples in thin, skin-mounted electrophysiological sensors with mechanics precisely matched to the human epidermis and in soft, hydrogel-based vehicles for triggered drug release suggest their broad potential uses in biomedical devices.

Size tailoring of aqueous germanium nanoparticle dispersions.

We demonstrate a practical route to synthesize Ge nanoparticles (NPs) in multi-gram quantities via the laser pyrolysis of GeH4 gas. The size of the as-produced Ge NPs can be precisely controlled in the range of 19.0 to 65.9 nm via a subsequent etching procedure using a dilute H2O2 solution. Stable water dispersions of Ge NPs yield particles with a Ge/GeO2 core-shell structure, however, the oxide shell can easily be removed and passivated by treatment with HCl. The feed materials used in this process are readily available and lead to non-toxic, water-based dispersions of Ge NPs. The scalability and convenience of this procedure make it attractive as a method to obtain Ge NP dispersions for use in applications such as optoelectronic devices and biosensors.

Synthesis of PCDTBT-based fluorinated polymers for high open-circuit voltage in organic photovoltaics: towards an understanding of relationships between polymer energy levels engineering and ideal morphology control.

The introduction of fluorine (F) atoms onto conjugated polymer backbone has verified to be an effective way to enhance the overall performance of polymer-based bulk-heterojunction (BHJ) solar cells, but the underlying working principles are not yet fully uncovered. As our attempt to further understand the impact of F, herein we have reported two novel fluorinated analogues of PCDTBT, namely, PCDTFBT (1F) and PCDT2FBT (2F), through inclusion of either one or two F atoms into the benzothiadiazole (BT) unit of the polymer backbone and the characterization of their physical properties, especially their performance in solar cells. Together with a profound effect of fluorination on the optical property, nature of charge transport, and molecular organization, F atoms are effective in lowering both the HOMO and LUMO levels of the polymers without a large change in the energy bandgaps. PCDTFBT-based BHJ solar cell shows a power conversion efficiency (PCE) of 3.96 % with high open-circuit voltage (VOC) of 0.95 V, mainly due to the deep HOMO level (-5.54 eV). To the best of our knowledge, the resulting VOC is comparable to the record VOC values in single junction devices. Furthermore, to our delight, the best PCDTFBT-based device, prepared using 2 % v/v diphenyl ether (DPE) additive, reaches the PCE of 4.29 %. On the other hand, doubly-fluorinated polymer PCDT2FBT shows the only moderate PCE of 2.07 % with a decrease in VOC (0.88 V), in spite of the further lowering of the HOMO level (-5.67 eV) with raising the number of F atoms. Thus, our results highlight that an improvement in efficiency by tuning the energy levels of the polymers by means of molecular design can be expected only if their truly optimized morphologies with fullerene in BHJ systems are materialized.

A hybrid solar cell fabricated using amorphous silicon and a fullerene derivative.

Hybrid solar cells, based on organic and inorganic semiconductors, are a promising way to enhance the efficiency of solar cells because they make better use of the solar spectrum and are straightforward to fabricate. We report on a new hybrid solar cell comprised of hydrogenated amorphous silicon (a-Si:H), [6,6]-phenyl-C71-butyric acid methyl ester ([71]PCBM), and poly-3,4-ethylenedioxythiophene poly styrenesulfonate (PEDOT:PSS). The properties of these PEDOT:PSS/a-Si:H/[71]PCBM devices were studied as a function of the thickness of the a-Si:H layer. It was observed that the open circuit voltage and the short circuit current density of the device depended on the thickness of the a-Si:H layer. Under simulated one sun AM 1.5 global illumination (100 mW cm(-2)), a power conversion efficiency of 2.84% was achieved in a device comprised of a 274 nm-thick layer of a-Si:H; this is the best performance achieved to date for a hybrid solar cell made of amorphous Si and organic materials.

Toward the Realization of a practical diketopyrrolopyrrole-based small molecule for improved efficiency in ternary BHJ solar cells.

An easily accessible DPP-based small molecule (DMPA-DTDPP) has been synthesized by a simple and efficient route. The resulting molecule, when incorporated into a P3HT:PCBM-based BHJ solar cell, is found to significantly improve the efficiency. The utility of DMPA-DTDPP as an additive yields an increase in the short circuit current density (Jsc) because DMPA-DTDPP serves as an energy funnel for P3HT excitons at the P3HT:PCBM interfaces, resulting in an improved overall power conversion efficiency, compared to the P3HT:PCBM control device. Considering the trouble-free and cost effective synthesis of DMPA-DTDPP, it may prove very useful in high-performance solar cells.

Copolymers comprising 2,7-carbazole and bis-benzothiadiazole units for bulk-heterojunction solar cells.

On the basis of theoretical considerations of the intramolecular charge transfer (ICT) effect, we have designed a series of donor (D)-acceptor (A) conjugated polymers based on bis-benzothiadiazole (BBT). A PPP-type copolymer of electron-rich 2,7-carbazole (CZ) and electron-deficient BBT units poly[N-(2-decyltetradecyl)-2,7-carbazole-co-7,7'-{4,4'-bis-(2,1,3-benzothiadiazole)}] (PCZ-BBT), a PPV-type copolymer poly[N-(2-decyltetradecyl)-2,7-carbazolevinylene-co-7,7'-{4,4'-bis-(2,1,3-benzothiadiazolevinylene)}] (PCZV-BBTV), and a tercopolymer based on carbazole, thiophene, and BBT poly[N-(2-decyltetradecyl)-2,7-(di-2-thienyl)carbazole-co-7,7'-{4,4'-bis-(2,1,3-benzothiadiazole)}] (PDTCZ-BBT) have been synthesized to understand the influence of BBT acceptor structure and linkage on the photovoltaic characteristics of the resulting materials. Both the HOMO and LUMO of the resulting polymers are found to be deeper-lying than those of benzothiadiazole-based polymers. The measured electrochemical band gaps (eV) are in the following order: PDTCZ-BBT (1.65 eV) < PCZV-BBTV (1.69 eV) < PCZ-BBT (1.75 eV). All the polymers provide a photovoltaic response when blended with a fullerene derivative as an electron acceptor. The best cell reaches a power conversion efficiency of 2.07 % estimated under standard solar light conditions (AM1.5G, 100 mW cm(-2)). We demonstrate for the first time that BBT-based polymers are promising materials for use in bulk-heterojunction solar cells.

A synthetic approach to a fullerene-rich dendron and its linear polymer via ring-opening metathesis polymerization.

Through the esterification of an acyl chloride functionalized fullerene precursor with dendritic alcohol, a fullerene-rich dendron containing a norbornene unit at the focal point is prepared for ring-opening metathesis polymerization to obtain its linear polymer with a unimodal and narrow molar mass distribution (PDI = 1.08) by a progressive addition of catalysts.