Pruittcummings0025

Photocatalytic CO2 conversion into reproducible chemical fuels (e.g., CO, CH3OH, or CH4) provides a promising scheme to solve the increasing environmental problems and energy demands simultaneously. However, the efficiency is severely restricted by the high overpotential of the CO2 reduction reaction (CO2RR) and rapid recombination of photoexcited carriers. Here, we propose that a novel type-II photocatalytic mechanism based on two-dimensional (2D) ferroelectric multilayers would be ideal for addressing these issues. Using density-functional theory and nonadiabatic molecular dynamics calculations, we find that the ferroelectric CuInP2S6 bilayers exhibit a staggered band structure induced by the vertical intrinsic electric fields. Different from the traditional type-II band alignment, the unique structure of the CuInP2S6 bilayer not only effectively suppresses the recombination of photogenerated electron-hole (e-h) pairs but also produces a sufficient photovoltage to drive the CO2RR. The predicted recombination time of photogenerated e-h pairs, 1.03 ns, is much longer than the transferring times of photoinduced electrons and holes, 5.45 and 0.27 ps, respectively. Moreover, the overpotential of the CO2RR will decrease by substituting an S atom with a Cu atom, making the redox reaction proceed spontaneously under solar radiation. The solar-to-fuel efficiency with an upper limit of 8.40% is achieved in the CuInP2S6 bilayer and can be further improved to 32.57% for the CuInP2S6 five-layer. Our results indicate that this novel type-II photocatalytic mechanism would be a promising way to achieve highly efficient photocatalytic CO2 conversion based on the 2D ferroelectric multilayers.Solid-state lithium batteries (SSLBs) based on garnet-type solid-state electrolytes (SSEs) have attracted much attention due to their high energy density and chemical stability. However, poor room-temperature ionic conductivity and low density of SSEs induced by conventional preparation routes limit their potential future applications. In this work, an oriented attachment strategy is employed to enhance the Li-ion conductivity and density of garnet-type SSE Li6.5La3Zr1.5Ta0.5O12 by introducing La2O3 nanoparticles. The oriented attachment of the ZrO2(Ta2O5) matrix mediates the epitaxial growth of the La-Zr(Ta)-O intermediate phase due to the addition of La2O3 nanoparticles. Continuous Li-ion transport pathways along grain boundaries are produced by the combination of residual La2O3 and gas Li2O. A densification interface is obtained when 10 wt % La2O3 is doped. The maximum value of Li-ion conductivity reaches 8.20 × 10-4 S·cm-1, with a relative density of 97.3%. SSLBs with a LiFePO4 cathode showing a stable cycling performance with a discharge capacity of 123.1 mA·h·g-1 and a Coulombic efficiency of 99.2% after 300 cycles (0.5C) at room temperature. This work is comparable to the state-of-the-art methodology, which provides a feasible approach to creating SSEs with high performances for SSLBs.Reversible solid oxide cells (RSOCs) present a conceivable potential for addressing energy storage and conversion issues through realizing efficient cycles between fuels and electricity based on the reversible operation of the fuel cell (FC) mode and electrolysis cell (EC) mode. Reliable electrode materials with high electrochemical catalytic activity and sufficient durability are imperatively desired to stretch the talents of RSOCs. Herein, oxygen vacancy engineering is successfully implemented on the Fe-based layered perovskite by introducing Zr4+, which is demonstrated to greatly improve the pristine intrinsic performance, and a novel efficient and durable oxygen electrode material is synthesized. The substitution of Zr at the Fe site of PrBaFe2O5+δ (PBF) enables enlarging the lattice free volume and generating more oxygen vacancies. Simultaneously, the target material delivers more rapid oxygen surface exchange coefficients and bulk diffusion coefficients. The performance of both the FC mode and EC mode is greatly enhanced, exhibiting an FC peak power density (PPD) of 1.26 W cm-2 and an electrolysis current density of 2.21 A cm-2 of single button cells at 700 °C, respectively. The reversible operation is carried out for 70 h under representative conditions, that is, in air and 50% H2O + 50% H2 fuel. Eventually, the optimized material (PBFZr), mixed with Gd0.1Ce0.9O2, is applied as the composite oxygen electrode for the reversible tubular cell and presents excellent performance, achieving 4W and 5.8 A at 750 °C and the corresponding PPDs of 140 and 200 mW cm-2 at 700 and 750 °C, respectively. The enhanced performance verifies that PBFZr is a promising oxygen electrode material for the tubular RSOCs.Lightweight SiBCN ceramic nanofibers were prepared by a combination of electrostatic spinning and high-temperature annealing techniques, showing tunable electromagnetic wave absorption. PF-04620110 Transferase inhibitor By controlling the annealing temperature, the nanoscale architectures and atomic bonding structures of as-prepared nanofibers could be well regulated. The resulting SiBCN nanofibers ∼300 nm in diameter, which were composed of an amorphous matrix, β-SiC, and free carbon nanocrystals, were defect-free after annealing at 1600 °C. SiBCN nanofibers annealed at 1600 °C exhibited good microwave absorption, obtaining a minimum reflection coefficient of -56.9 dB at 10.56 GHz, a sample thickness of 2.6 mm with a maximum effective absorption bandwidth of 3.45 GHz, and a maximum dielectric constant of 0.44. Owing to the optimized A + B + C microstructure, SiBCN ceramic nanofibers with satisfying microwave absorption properties endowed the nanofibers with the potential to be used as lightweight, ultrastrong radar wave absorbers applied in military and the commercial market.In situ stimuli-responsive molecular devices have gained much attention in biomedical areas due to their characteristics of increased image contrast and drug accumulation. Herein, we present a hand-in-hand in situ tile assembly for improved visualization of TK1 mRNA and killing of cancer cells. A pH-responsive and aptamer-functionalized tile motif (pH-Apt-TM) was first formed by four single-strand DNA, possessing pH-responsiveness and intracellular TK1 mRNA recognition capacity. When encountering target cells, the pH-Apt-TM could recognize target receptors on the cell surface through the aptamer domain. Meanwhile, the extracellular acidic pH gathered the pH-Apt-TM into a multifunctional hand-in-hand DNA tile assembly (HDTA) on the cells' surface. Compared to the pH-Apt-TM, studies revealed that the HDTA exhibited enhanced recognition, efficient cellular uptake, and improved visualization of TK1 mRNA, accompanied by gene silencing. Moreover, using Dox as a chemotherapeutic model, specific drug delivery and enhanced cell killing were achieved with target cells.