Nationwide-incidence and trends of fibromyalgia in South Korea: a population-based study.

Reports of the incidence of fibromyalgia (FM) in Asia are uncommon. Therefore, this study used nationwide representative data to investigate the age- and sex-specific incidence and annual trends of FM in South Korea. This nationwide population-based study used data from the Korean National Health Claims Database. From 2012 to 2021, patients with FM diagnosed according to the ACR 2010 criteria from the entire Korean population aged 20-70 years were included in the enrolment database. Age- and sex-specific cumulative and annual incidences were analyzed and incident cases from 2014 to 2021 were included, considering the 2-year washout period. Among the total cohort of 42 million in the entire Korean population, 270,160 had FM during the study period. The incidence in the general population aged 20-70 years was 751.25 (95% confidence interval [CI] 751.10-751.40) per 100,000 persons (men: 95% CI 608.45-608.98; women: 95% CI 898.02-898.69). The incidence of FM increased with advancing age, peaking at 50-54 years both in men and women. The annual incidence was 88.07 (95% CI 88.02-88.13) in 2014; it increased from 2014 to 2019 and peaked in 2019 (109.20; 95% CI 101.65-101.76). The incidence of FM in South Korea was about twice the global average, with a gradual increase over the study period. These detailed estimates can help with proper planning within the healthcare system.

Enhanced Power Conversion Efficiency of Dye-Sensitized Solar Cells by Band Edge Shift of TiO2 Photoanode.

By simple soaking titanium dioxide (TiO2) films in an aqueous Na2S solution, we could prepare surface-modified photoanodes for application to dye-sensitized solar cells (DSSCs). An improvement in both the open-circuit voltage (Voc) and the fill factor (FF) was observed in the DSSC with the 5 min-soaked photoanode, compared with those of the control cell without any modification. The UV-visible absorbance spectra, UPS valence band spectra, and dark current measurements revealed that the Na2S modification led to the formation of anions on the TiO2 surface, and thereby shifted the conduction band edge of TiO2 in the negative (upward) direction, inducing an increase of 29 mV in the Voc. It was also found that the increased FF value in the surface-treated device was attributed to an elevation in the shunt resistance.

Enhanced performance of polymer solar cells with a fluorocyanophenyl compound as an additive.

The efficiency of polymer solar cells (PSCs) with P3HT [poly(3-hexyl thiophene)]:PC61BM [[6,6]-phenyl C61-butyric acid methyl ester] blend film was improved by the incorporation of a fluorocyanophenyl compound, 3,4,5,6-tetrafluorophthalonitrile (TFP), as an additive. When the amount of TFTadditive was 5 wt% based on the total amount of P3HT and PC61BM, the highest efficiency was achieved. The annealed PSC with 5 wt% TFP had a power conversion efficiency of 4.45% compared with that (3.57%) of the reference cell without the additive, which corresponds to an increase of about 18.7% in the efficiency due to an enhancement in the short circuit current (J(sc)). A seriese of measurements such as UV-visible absorption spectroscopy, X-ray measurements, atomic force microscopic images and incident photon to current conversion efficiency (IPCE) spectra revealed that the increased J(sc) in the PSC with P3HT:PC61BM:TFP blend film was due to an improvement in both exciton generation and charge transport efficiency, resulting from higher absorbance, larger crystal size and more effective phase separation.

Improved photovoltaic properties of polymer solar cells with a phenyl compound as an additive.

A phenyl compound with electron withdrawing substituents, 3-fluoro-4-cyanophenol (FCP), was used as an additive in polymer solar cells with a P3HT [poly(3-hexyl thiophene)]:PCBM [[6,6]-phenyl-C61-butyric acid methyl ester] blend film. Under simulated solar illumination of AM 1.5 (100 mW/cm2), the devices fabricated using a P3HT:PCBM (1:0.9 w:w) layer blended with 5 wt% of FCP achieved an enhanced power conversion efficiency (PCE) of 4.8% due to the improved short circuit current and fill factor, as compared to reference cells with PCE = 4.1%. UV-visible absorption spectra, X-ray measurements and carrier mobility studies revealed that FCP facilitated the ordering of the P3HT chains, resulting in higher absorbance, larger crystal size, closer packing and enhanced hole mobility.

Efficient inverted bulk-heterojunction polymer solar cells with self-assembled monolayer modified zinc oxide.

The performance of poly(3-hexylthiophen) (P3HT) and [6, 6]phenyl C61 butyric acid methyl ester ([60]PCBM)-based inverted bulk-heterojunction (BHJ) polymer solar cells (PSCs) is enhanced by the modification of zinc oxide (ZnO)/BHJ interface with carboxylic-acid-functionalized self-assembled monolayers (SAMs). Under simulated solar illumination of AM 1.5 (100 mW/cm2), the inverted devices fabricated with SAM-modified ZnO achieved an enhanced power conversion efficiency (PCE) of 3.34% due to the increased fill factor and photocurrent density as compared to unmodified cells with PCE of 2.60%. This result provides an efficient method for interface engineering in inverted BHJ PSCs.

Wavelength-Tunable and Water-Stable Cesium-Lead-Based All-Bromide Nanocrystal-Polymer Composite Films Using Ultraviolet-Curable Prepolymer as an Anti-Solvent.

All-inorganic metal halide perovskite nanocrystals (IPeNCs) have become one of the most promising luminescent materials for next-generation display and lighting technology owing to their excellent color expression ability. However, research on IPeNCs with stable blue emission is limited. In this paper, we report stable blue emissive all-bromide IPeNCs obtained through a modified ligand-assisted reprecipitation method using an ultraviolet (UV)-curable prepolymer as the anti-solvent at a low temperature. We found that the blue emission originates from quantum-confined CsPbBr3 nanoparticles formed together with the colorless wide-bandgap Cs4PbBr6 nanocrystals. When the temperature of the prepolymer was increased from 0 to 50 °C, CsPbBr3 nanoparticles became larger and more crystalline, thereby altering their emission color from blue to green. The synthesized all-bromide blue-emitting IPeNC solution remained stable for over 1 h. It also remained stable when it was mixed with the green-emitting IPeNC solution. By simply exposing the as-synthesized IPeNC-prepolymer solutions to UV light, we formed water-stable composite films that emitted red, green, blue, and white colors. We believe that this synthetic method can be used to develop color-emitting composite materials that are highly suitable for application as the color conversion films of full-color liquid crystal display backlight systems and lighting applications.

Enhanced Light Absorption by Facile Patterning of Nano-Grating on Mesoporous TiO2 Photoelectrode for Cesium Lead Halide Perovskite Solar Cells.

CsPbIBr2, a cesium-based all-inorganic halide perovskite (CsPe), is a very promising alternative material to mainstream organic-inorganic hybrid halide perovskite (HPe) materials owing to its exceptional moisture stability, thermal stability, and light stability. However, because of the wide band gap (2.05 eV) of CsPbIBr2, it has a low power conversion efficiency (PCE), which hinders its application in highly efficient solar cells. In this study, a facile nanoimprinted one-dimensional grating nanopattern (1D GNP) formation on mesoporous TiO2 (mp-TiO2) photoelectrodes was introduced to improve the effective light utilization and enhance the performance of CsPbIBr2 perovskite solar cells (PSCs). The 1D GNP structure on the mp-TiO2 layer increases the light absorption efficiency by diffracting the unabsorbed light into the active mp-TiO2 and CsPbIBr2 layers as well as increasing the charge separation and collection due to the extended interfacial contact area between the mp-TiO2 and CsPbIBr2 layers. Consequently, both the current density (JSC) and the fill factor (FF) of the fabricated cells improved, leading to over a 20% enhancement in the solar cell's PCE. Thus, this periodic grating structure, fabricated by simple nanoimprinting, could play an important role in the large-scale production of highly efficient and cost-effective Cs-based PSCs.

Efficient TiO2 Surface Treatment Using Cs2CO3 for Solution-Processed Planar-Type Sb2S3 Solar Cells.

We report a highly effective surface treatment method for planar-type Sb2S3 solar cells by employing a Cs2CO3-modified compact TiO2 (c-TiO2) electron transport layer. It is found that surface treatment using a Cs2CO3 solution can shift the work function of c-TiO2 upward and reduce its surface roughness. As a result, compared with the power conversion efficiency of untreated solar cells, that of the treated solar cells with a glass/FTO/c-TiO2(/Cs2CO3)/Sb2S3/P3HT/Au structure significantly improved from 2.83 to 3.97%. This study demonstrates that the introduction of Cs2CO3 on a c-TiO2 layer is a simple and efficient way to adjust the work function of the electron transport layer and fabricate high-performance planar-type Sb2S3 solar cells.

Photovoltaic Performance of Dye-Sensitized Solar Cells Containing ZnO Microrods.

At an elevated temperature of 90 °C, a chemical bath deposition using an aqueous solution of Zn(NO3)2·6H2O and (CH2)6N4 resulted in the formation of both nanoflowers and microrods of ZnO on F-doped SnO2 glass with a seed layer. The nanoflowers and microrods were sensitized with dyes for application to the photoelectrodes of dye-sensitized solar cells (DSSCs). By extending the growth time of ZnO, the formation of nanoflowers was reduced and the formation of microrods favored. As the growth time was increased from 4 to 6 and then to 8 h, the open circuit voltage (Voc) values of the DSSCs were increased, whilst the short circuit current (Jsc) values varied only slightly. Changes in the dye-loading amount, dark current, and electrochemical impedance were monitored and they revealed that the increase in Voc was found to be due to a retardation of the charge recombination between photoinjected electrons and I3- ions and resulted from a reduction in the surface area of ZnO microrods. A reduced surface area decreased the dye contents adsorbed on the ZnO microrods, and thereby decreased the light harvesting efficiency (LHE). An increase in the electron collection efficiency attributed to the suppressed charge recombination counteracted the decreased LHE, resulting in comparable Jsc values regardless of the growth time.

Inverted polymer fullerene solar cells exceeding 10% efficiency with poly(2-ethyl-2-oxazoline) nanodots on electron-collecting buffer layers.

Polymer solar cells have been spotlighted due to their potential for low-cost manufacturing but their efficiency is still less than required for commercial application as lightweight/flexible modules. Forming a dipole layer at the electron-collecting interface has been suggested as one of the more attractive approaches for efficiency enhancement. However, only a few dipole layer material types have been reported so far, including only one non-ionic (charge neutral) polymer. Here we show that a further neutral polymer, namely poly(2-ethyl-2-oxazoline) (PEOz) can be successfully used as a dipole layer. Inclusion of a PEOz layer, in particular with a nanodot morphology, increases the effective work function at the electron-collecting interface within inverted solar cells and thermal annealing of PEOz layer leads to a state-of-the-art 10.74% efficiency for single-stack bulk heterojunction blend structures comprising poly[4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b']dithiophene-alt-3-fluorothieno[3,4-b]thiophene-2-carboxylate] as donor and [6,6]-phenyl-C71-butyric acid methyl ester as acceptor.

Pronounced Cosolvent Effects in Polymer:Polymer Bulk Heterojunction Solar Cells with Sulfur-Rich Electron-Donating and Imide-Containing Electron-Accepting Polymers.

The performance of solar cells with a polymer:polymer bulk heterojunction (BHJ) structure, consisting of poly[4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b']dithiophene-alt-3-fluorothieno[3,4-b]thiophene-2-carboxylate] (PTB7-Th) donor and poly[[N,N'-bis(2-octyldodecyl)-naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl]-alt-5,5'-(2,2'-bithiophene)] (P(NDI2OD-T2)) acceptor polymers, was investigated as a function of cosolvent (p-xylene:chlorobenzene (pXL:CB)) composition ratio. A remarkable efficiency improvement (∼38%) was achieved by spin-coating the photoactive blend layer from pXL:CB = 80:20 (volume) rather than pXL alone, but the efficiency then decreased when the CB content increased further to pXL:CB = 60:40. The improved efficiency was correlated with a particular PTB7-Th:P(NDI2OD-T2) donor-acceptor blend nanostructure, evidenced by a fiber-like surface morphology, a red-shifted optical absorption, and enhanced PL quenching. Further device optimization for pXL:CB = 80:20 films yielded a power conversion efficiency of ∼5.4%. However, these devices showed very poor stability (∼15 min for a 50% reduction in initial efficiency), owing specifically to degradation of the PTB7-Th donor-component. Replacing PTB7-Th with a more stable donor polymer will be essential for any application potential to be realized.

Molecular cloning and characterization of an NADPH quinone oxidoreductase from Kluyveromyces marxianus.

NAD(P)H quinone oxidoreductase is a ubiquitous enzyme that is known to directly reduce quinone substrates to hydroquinones by a two-electron reaction. We report the identification of NADPH quinone oxidoreductase from Kluyveromyces marxianus (KmQOR), which reduces quinone substrates directly to hydroquinones. The KmQOR gene was sequenced, expressed in Escherichia coli, purified, and characterized. The open-reading frame of the KmQOR gene consists of 1143 nucleotides, encoding a 380 amino acid polypeptide. The nucleotide sequence of the KmQOR gene was assigned to EMBL under accession number AY040868. The M(r) that was determined by SDS-PAGE for the protein subunit was about 42 kDa, and the molecular mass of the native KmQOR was 84 kDa, as determined by column calibration, indicating that the native protein is a homodimer. The KmQOR protein efficiently reduced 1,4-benzoquinone, whereas no activities were found for menadiones and methoxyquinones. These observations, and the result of an extended sequence analysis of known NADPH quinone oxidoreductase, suggest that KmQOR possesses a different action mechanism.

Simultaneous determination of levodopa and carbidopa by synchronous fluorescence spectrometry using double scans.

A synchronous fluorescence spectrometric method is described for the simultaneous determination of binary mixtures of levodopa and carbidopa in pharmaceutical formulation and urine sample, without prior separation steps, using two scans. At Delta lambda = 30 nm, only carbidopa yields a detectable signal that is independent of the presence of levodopa. Similarly, at Delta lambda = 65 nm the signal of levodopa is not influenced by the presence of carbidopa. Signals at two wavelengths, 288 nm (Delta lambda = 30 nm) and 281 nm (Delta lambda = 65 nm), vary linearly with carbidopa and levodopa concentrations over the range 0.019-1.971 microg mL(-1) (for levodopa) and 0.022-2.262 microg mL(-1) (for carbidopa), respectively. The correlation coefficients for the standard calibration graphs were 0.9962 and 0.9951 (n=10) for carbidopa and levodopa, respectively. The limits of detection (LOD estimated as per IUPAC recommendations) were 0.01 and 0.006 microg mL(-1) for carbidopa and levodopa, respectively. The method was successfully applied to the determination of levodopa and carbidopa in pharmaceutical formulation and urine sample. The recovery results were satisfactory.