RESUMO
OBJECTIVE: Perioperative neurocognitive disorders (PND) are a group of prevalent neurological complications that often occur in elderly individuals following major or emergency surgical procedures. The etiologies are not fully understood. This study endeavored to investigate novel targets and prediction methods for the occurrence of PND. METHODS: A total of 229 elderly patients diagnosed with prostatic hyperplasia who underwent transurethral resection of the prostate (TURP) combined with spinal cord and epidural analgesia were included in this study. The patients were divided into two groups, the PND group and non-PND group, based on the Z-score method. According to the principle of maintaining consistency between preoperative and intraoperative conditions, three patients from each group were randomly chosen for serum sample collection. isobaric tags for relative and absolute quantification (iTRAQ) proteomics technology was employed to analyze and identify the proteins that exhibited differential expression in the serum samples from the two groups. Bioinformatics analysis was performed on the proteins that exhibited differential expression. RESULTS: Among the 1101 serum proteins analyzed in the PND and non-PND groups, eight differentially expressed proteins were identified in PND patients. Of these, six proteins showed up-regulation, while two proteins showed down-regulation. Further bioinformatics analysis of the proteins that exhibited differential expression revealed their predominant involvement in cellular biological processes, cellular component formation, as well as endocytosis and phagocytosis Additionally, these proteins were found to possess the RING domain of E3 ubiquitin ligase. CONCLUSION: The iTRAQ proteomics technique was employed to analyze the variation in protein expression in serum samples from patients with PND and those without PND. This study successfully identified eight proteins that exhibited differential expression levels between the two groups. Bioinformatics analysis indicates that proteins exhibiting differential expression are primarily implicated in the biological processes associated with microtubules. Investigating the microtubule formation process as it relates to neuroplasticity and synaptic formation may offer valuable insights for enhancing our comprehension and potential prevention of PND. CLINICAL TRIAL REGISTRATION: Registered (ChiCTR2000028836). Date (20190306).
Assuntos
Ressecção Transuretral da Próstata , Humanos , Masculino , Idoso , Ressecção Transuretral da Próstata/efeitos adversos , Proteômica , Hiperplasia Prostática/cirurgia , Hiperplasia Prostática/sangue , Transtornos Neurocognitivos/etiologia , Transtornos Neurocognitivos/sangue , Transtornos Neurocognitivos/metabolismo , Complicações Cognitivas Pós-Operatórias/etiologia , Complicações Cognitivas Pós-Operatórias/sangue , Período Perioperatório , Idoso de 80 Anos ou mais , Proteínas Sanguíneas/metabolismo , Proteínas Sanguíneas/análise , Biologia ComputacionalRESUMO
Solar energy is the most abundant renewable energy available to the earth and can meet the energy needs of humankind, but efficient conversion of solar energy to electricity is an urgent issue of scientific research. As the third-generation photovoltaic technology, dye-sensitized solar cells (DSSCs) have gained great attention since the landmark efficiency of â¼7% reported by O'Regan and Grätzel. The most attractive features of DSSCs include low cost, simple manufacturing processes, medium-purity materials, and theoretically high power conversion efficiencies. As one of the key materials in DSSCs, the counter electrode (CE) plays a crucial role in completing the electric circuit by catalyzing the reduction of the oxidized state to the reduced state for a redox couple (e.g., I3-/I-) in the electrolyte at the CE-electrolyte interface. To lower the cost caused by the typically used Pt CE, which restricts the large-scale application because of its low reserves and high price, great effort has been made to develop new CE materials alternative to Pt. A lot of Pt-free electrocatalysts, such as carbon materials, inorganic compounds, conductive polymers, and their composites with good electrocatalytic activity, have been applied as CEs in DSSCs in the past years. Metal selenides have been widely used as electrocatalysts for the oxygen reduction reaction and light-harvesting materials for solar cells. Our group first expanded their applications to the DSSC field by using in situ-grown Co0.85Se nanosheet and Ni0.85Se nanoparticle films as CEs. This finding has inspired extensive studies on developing new metal selenides in order to seek more efficient CE materials for low-cost DSSCs, and a lot of meaningful results have been achieved in the past years. In this Account, we summarize recent advances in binary and mutinary metal selenides applied as CEs in DSSCs. The synthetic methods for metal selenides with various morphologies and stoichiometric ratios and deposition methods for CE films are described. We emphasize that the in situ growth method exhibits advantages over other methods for fabricating stable and efficient CEs. We focus on the effect of morphology on the electocatalytic and photovoltaic performance. Application of transparent metal selenide CEs in bifacial DSSCs and the superiority of in situ-grown metal selenide nanosheet fiber CEs used for fiber DSSCs are presented. In addition, we show that metal selenides with a hollow sphere structure can function not only as an efficient electrocatalyst but also as a light-scattering layer. Finally, we present our views on the current challenges and future development of metal selenide CE materials.
RESUMO
To improve the interfacial charge transfer that is crucial to the performance of perovskite solar cells, the interface engineering in a device should be rationally designed. Here we have developed an interface engineering method to tune the photovoltaic performance of planar-heterojunction perovskite solar cells by incorporating MAPbBr3-xIx (MA = CH3NH3) quantum dots (QDs) between the MAPbI3 perovskite film and the hole-transporting material (HTM) layer. By adjustment of the Br:I ratio, the as-synthesized MAPbBr3-xIx QDs show tunable fluorescence and band edge positions. When the valence band (VB) edge of MAPbBr3-xIx QDs is located below that of the MAPbI3 perovskite, the hole transfer from the MAPbI3 perovskite film to the HTM layer is hindered, and hence, the power conversion efficiency decreases. In contrast, when the VB edge of MAPbBr3-xIx QDs is located between the VB edge of the MAPbI3 perovskite film and the highest occupied molecular orbital of the HTM layer, the hole transfer from the MAPbI3 perovskite film to the HTM layer is well-facilitated, resulting in significant improvements in the fill factor, short-circuit photocurrent, and power conversion efficiency.
RESUMO
To obtain a broad spectral response in the visible region, TiO2 film is co-sensitized with a porphyrin dye (FNE57 or FNE59) and an organic dye (FNE46). It is found that the stepwise co-sensitization in one single dye solution followed by in another single dye solution is better than the co-sensitization in a cocktail solution in terms of photovoltaic performance. The stepwise co-sensitization first with a porphyrin dye and then with an organic dye outperforms that in a reverse order. DSSC devices based on co-sensitizers FNE57 + FNE46 and FNE59 + FNE46 with a quasi-solid-state gel electrolyte generate power conversion efficiencies of 7.88% and 8.14%, respectively, which exhibits remarkable efficiency improvements of 61% and 35%, as compared with devices sensitized with the porphyrin dyes FNE57 and FNE59, respectively. Co-sensitization brings about a much improved short-circuit photocurrent due to the complementary absorption of the two sensitizers. The observed enhancement of incident monochromatic photon-to-electron conversion efficiency from individual dye sensitization to co-sensitization is attributed to the improved charge collection efficiency rather than to the light harvesting efficiency. Interestingly, the open-circuit photovoltage for the co-sensitization system comes between the higher voltage for the porphyrin dye (FNE57 or FNE59) and the lower voltage for the organic dye (FNE46), which is well correlated with their electron lifetimes. This finding indicates that not only the spectral complementation but also the electron lifetime should be considered to select dyes for co-sensitization.
RESUMO
Lead halide perovskites have achieved phenomenal successes in photovoltaics due to their suitable bandgaps, long diffusion lengths, and balanced charge transport. However, the extreme susceptibility of perovskites to water or air has imposed a seemingly insurmountable barrier for leveraging these unique materials into solar-to-fuel applications such as photoelectrochemical conversion. Here we developed a CH3NH3PbI3-based photoanode with an ultrathin Ni surface layer, which functions as both a physical passivation barrier and a hole-transferring catalyst. Remarkably, a much enhanced photocurrent density, an unassisted photoelectrochemical conversion capability, and a substantially better stability against water have been achieved, which are exceeding most of the previously reported photoanodes as well as a similar CH3NH3PbI3-based device structure but without the Ni surface layer. Our study suggests many exciting opportunities of developing perovskite-based solar-to-fuel conversion.
RESUMO
A simple and versatile hydrothermal method is developed to synthesize Cu-Cu2O, in which Cu particles grow on the surface of a Cu2O truncated octahedron. Through the reduction of Cu(2+) by glucose in an alkaline solution, the Cu2O truncated octahedron is quickly formed via a kinetic control process, and then Cu particles selectively nucleate on the high-energy (110) facets of Cu2O, generating a heterostructure. The amount of Cu in the sample is successfully tuned by varying the reaction temperature. Compared to Cu2O, the hybrid Cu-Cu2O architecture shows superior electrocatalytic performance for glucose oxidation due to the synergistic effect between more electrocatalytic active but less conductive Cu2O and more conductive but less electrocatalytic active Cu. By tuning the content of Cu in the heterostructure, the highest electrocatalytic activity is achieved at the Cu/Cu2O molar ratio of 0.83.
Assuntos
Cobre/química , Glucose/química , Catálise , Espectroscopia Dielétrica , Oxirredução , Tamanho da Partícula , Propriedades de Superfície , TemperaturaRESUMO
Pseudolarix (Pinaceae) is a vulnerable (sensu IUCN) monotypic genus restricted to southeastern China. To better understand levels of genetic diversity, population structure and gene flow among populations of P. amabilis, we developed five compound SSR markers and ten novel polymorphic expressed sequence tags (EST) derived microsatellites. The results showed that all 15 loci were polymorphic with the number of alleles per locus ranging from two to seven. The expected and observed heterozygosities varied from 0.169 to 0.752, and 0.000 to 1.000, respectively. The inbreeding coefficient ranged from -0.833 to 1.000. These markers will contribute to research on genetic diversity and population genetic structure of P. amabilis, which in turn will contribute to the species conservation.
Assuntos
Repetições de Microssatélites , Pinaceae/genética , Sequência de Bases , Etiquetas de Sequências Expressas , Genes de Plantas , Marcadores Genéticos , Polimorfismo Genético , Análise de Sequência de DNARESUMO
A series of symmetrical donor-acceptor-donor (D-A-D) chromophores bearing various electron-withdrawing groups, such as quinoxaline (Qx), benzo[g]quinoxaline (BQ), phenazine (Pz), benzo[b]phenazine (BP), thieno[3,4-b]pyrazine (TP), and thieno[3,4-b]quinoxaline (TQ), has been designed and synthesized. Intramolecular charge transfer (ICT) interactions can be found for all the chromophores due to the electron-withdrawing properties of the two imine nitrogens in the pyrazine ring and the electron-donating properties of the other two amine nitrogens in the two triphenylamines. Upon the fusion of either benzene or thiophene ring on the pyrazine acceptor unit, the ICT interactions are strengthened, which results in the bathochromically shifted ICT band. Moreover, the thiophene ring is superior to the benzene ring in enlarging the ICT interaction and expanding the absorption spectrum. Typically, when a thiophene ring is fused on the Qx unit in DQxD, a near-infrared dye is realized in simple chromophore DTQD, which displays the maximum absorption wavelength at 716 nm with the threshold over 900 nm. This is probably due to the enhanced charge density on the acceptor moiety and better orbital overlap, as revealed by theoretical calculation. These results suggest that extending the conjugation of a pyrazine acceptor in an orthogonal direction to the D-A-D backbone can dramatically improve the ICT interactions.
RESUMO
To minimize the charge recombination between electrons and the electron acceptor in solid-state dye-sensitized solar cells, we propose a separated electron donor and acceptor of a redox couple in the photoanode and in the cathode, respectively. Owing to the absence of the acceptor in the photoanode initially, the charge recombination rate is retarded remarkably, resulting in an increase of the short-circuit photocurrent by >2-fold, open-circuit photovoltage by 71 mV and power conversion efficiency by >2.5-fold.
RESUMO
Photovoltaic devices represent an efficient electricity generation mode. Integrating them into textiles offers exciting opportunities for smart electronic textiles-with the ultimate goal of supplying power for wearable technology-which is poised to change how electronic devices are designed. Many human activities occur indoors, so realizing indoor photovoltaic fibers (IPVFs) that can be woven into textiles to power wearables is critical, although currently unavailable. Here, a dye-sensitized IPVF is constructed by incorporating titanium dioxide nanoparticles into aligned nanotubes to produce close contact and stable interfaces among active layers on a curved fiber substrate, thus presenting efficient charge transport and low charge recombination in the photoanode. With the combination of highly conductive core-sheath Ti/carbon nanotube fiber as a counter electrode, the IPVF shows a certified power conversion efficiency of 25.53% under 1500 lux illuminance. Its performance variation is below 5% after bending, twisting, or pressing for 1000 cycles. These IPVFs are further integrated with fiber batteries as self-charging power textiles, which are demonstrated to effectively supply electricity for wearables, solving the power supply problem in this important direction.
RESUMO
Imidazolium iodide is an often used component in iodine-based dye-sensitized solar cells (DSSCs), but it cannot operate an efficient DSSC in the absence of iodine due to its low conductivity. For this study, lamellar solid iodide salts of imidazolium or piperidinium with an N-substituted propargyl group have been prepared and applied in solid-state DSSCs. Owing to the high conductivity arising from the lamellar structure, these solid-state ionic conductors can be used as single-component solid electrolytes to operate solid-state DSSCs efficiently without any additives in the electrolyte and post-treatments on the dye-loaded TiO2 films. With a propargyl group attached to the imidazolium ring, the conductivity is enhanced by about 4 × 10(4)-fold as compared to the alkyl-substituted imidazolium iodide. Solid-state DSSC with the 1-propargyl-3-methylimidazolium iodide as the single-component solid-state electrolyte has achieved a light-to-electricity power conversion efficiency of 6.3% under illumination of simulated AM1.5G solar light (100 mW cm(-2)), which also exhibits good long-term stability under continuous 1 sun soaking for 1500 h. This finding paves the way for development of high-conductivity single-component solid electrolytes for use in efficient solid-state DSSCs.
RESUMO
In this work, reduced graphene oxide (RGO) sheets are successfully introduced into the conductive polypyrrole (PPy) matrix as conductive channels and co-catalyst, through simple incorporation of graphene oxide (GO) into PPy and subsequent in situ reduction from GO/PPy to RGO/PPy composite film. The RGO/PPy film is fabricated as a counter electrode for dye-sensitized solar cells, and it exhibits excellent catalytic performance for reduction of triiodide. For this reason, the incorporated RGO sheets significantly improve short-circuit photocurrent density from 14.27 to 15.81 mA cm(-2) and power conversion efficiency from 7.11% to 8.14%, which is comparable with that for the cell based on a Pt cathode.
RESUMO
Although annealing is a commonly used crystallization method for perovskite films in perovskite solar cells (PSCs), the high thermal energy consumption and limitations on flexible devices hinder their further industrial application. We herein propose an annealing-free crystallization technology for perovskite films, assisted by the Zr-metal-organic framework (MOF) interface between SnO2 and the perovskite. It is found that the Zr-MOF interface can accelerate the formation of perovskite intermediates and promote their conversion into perovskite crystals even without annealing. The trap density thus decreases by about one fold, accompanied by significant increases in electron and hole mobilities, resulting in enhanced carrier extraction and suppressed charge recombination. Therefore, the Zr-MOF-based PSC attains a power convention efficiency (PCE) of 20.24%, 2.2 times that (9.26%) of the pristine PSC. Furthermore, the Zr-MOF interface layer can significantly improve the air and thermal stabilities of PSCs. The Zr-MOF-based PSC exhibits 93% of its initial PCE versus 52% for the pristine PSC after 1018 h of storage in air. Additionally, after 360 h of continuous heating at 65 °C, the Zr-MOF-based PSC retains 91% of its initial PCE against 44% for the pristine PSC.
RESUMO
We present herein a facile one-step low-temperature hydrothermal approach for in situ growth of metal selenides (Co(0.85)Se and Ni(0.85)Se) on conductive glass substrates. The as-prepared metal selenides on conductive substrates can be used directly as transparent counter electrodes for dye-sensitized solar cells (DSSCs) without any post-treatments. It is found that graphene-like Co(0.85)Se exhibits higher electrocatalytic activity than Pt for the reduction of triiodide. As a consequence, the DSSC with Co(0.85)Se generates higher short-circuit photocurrent and power conversion efficiency (9.40%) than that with Pt.
RESUMO
Novel organic sensitizers containing a thieno[3,4-c]pyrrole-4,6-dione (TPD) moiety with triphenylamine or julolidine as the electron donor have been designed and synthesized for quasi-solid-state dye-sensitized solar cells (DSSCs). For comparison, two organic dyes based on a terthiophene spacer have also been synthesized. The absorption, electrochemical and photovoltaic properties of all sensitizers have been systematically investigated. We found that the incorporation of TPD is highly beneficial to broaden the absorption spectra of the organic sensitizers and prevent the intermolecular interaction. Therefore, the charge recombination possibility is reduced, which is revealed by the controlled intensity modulated photovoltage spectroscopy. A quasi-solid-state DSSC based on sensitizer FNE38 with TPD and triphenylamine moieties demonstrates a solar energy conversion efficiency of 4.71% under standard AM 1.5G sunlight without the use of coadsorbant agents.
RESUMO
Surface modification plays a crucial role in improving the efficiency of dye-sensitized solar cells (DSSCs), but the reported surface treatments are in general superior to the untreated TiO(2) but inferior to the typical TiCl(4)-treated TiO(2) in terms of solar cell performance. This work demonstrates a two-step treatment of the nanoporous titania surface with strontium acetate [Sr(OAc)(2)] and TiCl(4) in order, each step followed by sintering. An electronically insulating layer of SrCO(3) is formed on the TiO(2) surface via the Sr(OAc)(2) treatment and then a fresh TiO(2) layer is deposited on top of the SrCO(3) layer via the TiCl(4) treatment, corresponding to a double layer of Sr(OAc)(2)/TiO(2) coated on the TiO(2) surface. As compared to the typical TiCl(4)-treated DSSC, the Sr(OAc)(2)-TiCl(4) treated DSSC improves short-circuit photocurrent (J(sc)) by 17%, open-circuit photovoltage (V(oc)) by 2%, and power conversion efficiency by 20%. These results indicate that the Sr(OAc)(2)-TiCl(4) treatment is better than the often used TiCl(4) treatment for fabrication of efficient DSSCs. Charge density at open circuit and controlled intensity modulated photocurrent/photovoltage spectroscopy reveal that the two electrodes show almost same conduction band level but different electron diffusion coefficient and charge recombination rate constant. Owing to the blocking effect of the SrCO(3) layer on electron recombination with I(3)(-) ions, the charge recombination rate constant of the Sr(OAc)(2)-TiCl(4) treated DSSC is half that of the TiCl(4)-treated DSSC, accounting well for the difference of their V(oc). The improved J(sc) is also attributed to the middle SrCO(3) layer, which increases dye adsorption and may improve charge separation efficiency due to the blocking effect of SrCO(3) on charge recombination.
RESUMO
Three near infrared (NIR) metal-free organic sensitizers (FNE32, FNE34, FNE36) based on the thieno[3,4-b]pyrazine derivative have been designed and synthesized for application in quasi-solid-state dye-sensitized solar cells (DSSCs). These organic dyes demonstrate maximum absorption bands at 596-625 nm due to the presence of the thieno[3,4-b]pyrazine derivative, which facilitates the intramolecular electron transfer from the donor to the acceptor. Quasi-solid-state DSSCs based on FNE34 display efficient photoelectric conversion over the whole visible range extending into the NIR region up to 900 nm with maximum incident monochromatic photon-to-electron conversion efficiency (IPCE) of 77%, yielding a short-circuit photocurrent density of 16.24 mA cm(-2) and a power conversion efficiency of 5.30%. To the best of our knowledge, this is the highest efficiency for quasi-solid-state DSSCs based on an organic NIR dye. When exposed to one-sun illumination for 1000 h, the quasi-solid-state DSSC based on FNE34 exhibits good long-term stability with almost constant power conversion efficiency.
RESUMO
To improve the crystallization and meanwhile adjust the band levels of perovskites, we design and synthesize a novel organic molecule, 4,4'-(spiro[cyclopenta[1,2-b:5,4-b']dithiophene-4,2'-[1,3]dioxolane]-2,6-diyl)bis(N,N-bis(4-methoxyphenyl)aniline) (TM1), to dissolve in an antisolvent for the antisolvent engineering of perovskite solar cells (PSCs). The coordination interactions between TM1 and Pb2+ ions in perovskites and the hydrogen bonds between the O atoms in the methoxy of TM1 and the MA+ in perovskites are characterized with X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. Owing to these interactions, TM1 can improve the perovskite crystallization, which reduces the trap density, enhances the interfacial hole extraction, and retards charge recombination as well, boosting short-circuit photocurrent notably. TM1 also shifts the valence band of perovskites upward by 0.17 eV, which aligns better with the highest occupied molecular orbital of hole transport materials and thus increases the open-circuit photovoltage significantly. As a result, the power conversion efficiency is enhanced from 17.22 to 20.21% by TM1. Moreover, TM1 can also improve device stability significantly. These findings demonstrate that TM1 is a kind of functional material as an additive in an antisolvent for both crystallization improvement and energy level adjustment of perovskites toward highly efficient and stable PSCs.
RESUMO
As all-inorganic perovskite (CsPbI3-xBrx) is prone to phase transition from the α phase (black phase) to the δ phase (yellow phase) in a humid environment or under heating, improving the phase stability of all-inorganic perovskite of the black phase is one of the urgent problems to solve. Herein, 1,2-dimethyl-3-acetylimidazolium iodide (DMAII) is spin-coated onto the surface of CsPbI3-xBrx perovskite for use in p-i-n perovskite solar cells (PSCs). We find that the DMAII coating has two effects on the CsPbI3-xBrx perovskite film: surface passivation and phase stabilization of perovskite. Traps in the CsPbI3-xBrx perovskite film can be reduced significantly by DMAII passivation, resulting in enhanced hole extraction and suppressed charge recombination. Consequently, the power conversion efficiency (PCE) is improved from 10.81 to 13.14%. Moreover, the DMAII coating can significantly inhibit the phase transition from the α phase to the δ phase in a humid environment or under heating, as characterized by the X-ray diffraction pattern, UV-vis absorption spectrum, and film color. After exposing the CsPbI3-xBrx perovskite films to a humid atmosphere (relative humidity = 40-60%) for 6 h, the PCE decreases dramatically to only 0.12% of the initial PCE for the PSC without the DMAII coating, while the PCE maintains 80% of the initial PCE for the PSC with the DMAII coating. In addition, when the PSC devices are heated at 120 °C for 4 h, the control PSC shows a 96% decrease in PCE, while the PCE decay is only 9% for the DMAII-coated PSC. These findings indicate that carboxyl-substituted imidazolium iodide is a kind of promising material to not only passivate traps but also stabilize the black phase of all-inorganic perovskite.
RESUMO
Monolayer of PDDA/graphene/PDDA/H(2)PtCl(6) is fabricated on conductive glass using electrostatic layer-by-layer self-assembly technique, which is then converted to graphene/Pt monolayer for use as counter electrode in dye-sensitized solar cell (DSSC). As compared to the sputtered Pt counter electrode, the self-assembled monolayer reduces the Pt amount by about 1000-fold but exhibits comparable photovoltaic performance. This finding provides a new route to fabrication of cheap and efficient counter electrodes for flow-line production of DSSCs.