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Objective: The CABANA study shows that atrial fibrillation (AF) paitents younger than 65 years benefit more from the AF radiofrequency catheter ablation (RFCA) procedure. The aim of this study is to investigate the impact of inherent patent foramen ovale (PFO) with a Left-to-Right Shunt on the RFCA procedure in young AF patients. Methods: Based on the presence or absence of inherent PFO, the AF patients were divided into the PFO groups and the non-PFO group. Clinical follow-up was also investigated. Results: A total of 285 AF patients were enrolled. PFO was detected by TEE in 42 patients. The age of patients at initial AF onset was younger in the PFO group than in the non-PFO group (58.3 ± 8.9 vs. 62.3 ± 9.6 years, P = 0.012). There were more AF patients aged

In order to fabricate Al/Ni energetic structural materials (ESMs) with high energy density and mechanical properties, a novel approach of hot pressing and friction stir processing (HP-FSP) was employed in this study. The effects of rotational speed on microstructure, exothermic reactions and mechanical properties of Al/Ni ESMs were investigated. The microstructure characteristics were characterized via scanning electron microscopy, transmission electron microscopy and X-ray diffraction. Differential scanning calorimeter, quasi-static compression and microhardness tests were conducted to analyze the energy density and mechanical properties, respectively. The results showed that the compressive strength and the energy density of Al/Ni ESMs without friction stir processing (FSP) were 183 MPa and 1110 J/g, respectively. Numerous Ni particles were broken and elongated to irregular granules and fibrous microstructure during FSP procedure. As the rotational speed reached 800 rpm, the Al/Ni ESMs prepared by HP-FSP method exhibited excellent comprehensive properties with the compressive strength of 416 MPa and the energy density of 856 J/g. With the increasing rotational speed, the compressive strength, elastic modulus and maximum microhardness increased first and then decreased, and the energy density decreased gradually. It was found that the enhancement of mechanical strength was attributed to dislocation strengthening and second phase strengthening. The reduction of exothermic energy density was ascribed to the increasing heat input of FSP treatment, intensifying the reaction diffusion in Al/Ni interfaces and promoting the generation and proliferation of Al3Ni phases.

Industrial water splitting has long been suppressed by the sluggish kinetics of the oxygen evolution reaction (OER), which requires a catalyst to be efficient. Herein, we propose a molecular-level proton acceptor strategy to produce an efficient OER catalyst that can boost industrial-scale water splitting. Molecular-level phosphate (-PO4) group is introduced to modify the surface of PrBa0.5Ca0.5Co2O5+δ (PBCC). The achieved catalyst (PO4-PBCC) exhibits significantly enhanced catalytic performance in alkaline media. Based on the X-ray absorption spectroscopy results and density functional theory (DFT) calculations, the PO4 on the surface, which is regarded as the Lewis base, is the key factor to overcome the kinetic limitation of the proton transfer process during the OER. The use of the catalyst in a membrane electrode assembly (MEA) is further evaluated for industrial-scale water splitting, and it only needs a low voltage of 1.66 V to achieve a large current density of 1 A cm−2. This work provides a new molecular-level strategy to develop highly efficient OER electrocatalysts for industrial applications.

Abstract Spintronic terahertz (THz) emitters (STEs) based on magnetic heterostructures have emerged as promising THz sources. However, it is still a challenge to achieve a higher intensity STE to satisfy all kinds of practical applications. Herein, we report a STE based on Pt0.93(MgO)0.07/CoFeB nanofilm by introducing dispersed MgO impurities into Pt, which reaches a 200% intensity compared to Pt/CoFeB and approaches the signal of 500 μm ZnTe crystal under the same pump power. We obtain a smaller spin diffusion length of Pt0.93(MgO)0.07 and an increased thickness-dependent spin Hall angle relative to the undoped Pt. We also find that the thickness of a Pt layer leads to a drastic change in the interface role in the spintronic THz emission, suggesting that the underlying mechanism of THz emission enhancement is a combined effect of enhanced bulk spin hall angle and the interfacial skew scattering by MgO impurities. Our findings demonstrate a simple way to realize high-efficiency, stable, advanced spintronic THz devices.

The ligand engineering of inorganic lead halide perovskite quantum dots (PQDs) is an indispensable strategy to boost their photoluminescence stability, which is pivotal for optoelectronics applications. CsPbX3 (X = Cl, Br, I) PQDs exhibit exceptional optical properties, including high color purity and tunable bandgaps. Despite their promising characteristics, environmental sensitivity poses a challenge to their stability. This article reviews the solution-based synthesis methods with ligand engineering. It introduces the impact of factors like humidity, temperature, and light exposure on PQD’s instability, as well as in situ and post-synthesis ligand engineering strategies. The use of various ligands, including X- and L-type ligands, is reviewed for their effectiveness in enhancing stability and luminescence performance. Finally, the significant potential of ligand engineering for the broader application of PQDs in optoelectronic devices is also discussed.

Abstract With the CoO2 slabs consisting of Co4O4 cubane structure, layered NaxCoO2 are considered promising candidates for oxygen evolution reaction (OER) in alkaline media given their earth‐abundant and structural advantages. However, due to the strong adsorption of intermediates on the large basal planes, NaxCoO2 cannot meet the activity demands. Here, a novel one‐pot synthesis strategy is proposed to realize the high solubility of iron in NaxCoO2 in an air atmosphere. The optimist Na0.6Co0.9Fe0.1O2 exhibits enhanced OER activity compared to their pristine and other reported Fe‐doped NaxCoO2 counterparts. Such an enhancement is mainly ascribed to the abundant active sites on the activated basal planes and the participation of oxidized oxygen as active sites independently, which breaks the scaling relationship limit in the OER process. This work is expected to contribute to the understanding of the modification mechanism of Fe‐doped cobalt‐based oxides and the exploitation of layer‐structured oxides for energy application.

Soybean (Glycine max (Linn.) Merr.) is highly suitable as animal feed. The silage quality and microbial characteristics of soybean silage are still unclear. Forage soybean (HN389), at six different growth stages (R2-R7), were used as experimental materials to investigate the changes in fermentation, nutritional quality, and microbial characteristics of semidry silage after 0, 7, 14, 30, and 45 d. As the growth period extended, the content of crude protein (CP) and crude fat (EE) gradually increased, while the neutral detergent fiber (NDF) and the acid detergent fiber (ADF) content decreased. The pH value also decreased gradually with fermentation time, accompanied by increases in the proportion of ammonia-N and the content of lactic acid (LA) and acetic acid (AA). In addition, competitive inhibition was observed in the microbial fermentation. With the process of ensiling, Lactobacillus became the dominant bacterial species. The results indicate that the most active stage of fermentation during ensiling occurred within the first 7 days, the fermentation and nutritional quality of the soybean forage were improved, and the optimal mowing stage was the grain stage. Comparison of the microbial abundance showed that all microorganisms entered a stable stage at 30 days of silage. After storage, the dominant bacteria were Lactobacillus, Enterobacter, and Pantoea.

Abstract The origin of insulating ferromagnetism in epitaxial LaCoO3 films under tensile strain remains elusive despite extensive research efforts are devoted. Surprisingly, the spin state of its Co ions, the main parameter of its ferromagnetism, is still to be determined. Here, the spin state in epitaxial LaCoO3 thin films is systematically investigated to clarify the mechanism of strain‐induced ferromagnetism using element‐specific X‐ray absorption spectroscopy and dichroism. Combining with the configuration interaction cluster calculations, it is unambiguously demonstrated that Co3+ in LaCoO3 films under compressive strain (on LaAlO3 substrate) is practically a low‐spin state, whereas Co3+ in LaCoO3 films under tensile strain (on SrTiO3 substrate) have mixed high‐spin and low‐spin states with a ratio close to 1:3. From the identification of this spin state ratio, it is inferred that the dark strips observed by high‐resolution scanning transmission electron microscopy indicate the position of Co3+ high‐spin state, i.e., an observation of a spin state disproportionation in tensile‐strained LaCoO3 films. This consequently explains the nature of ferromagnetism in LaCoO3 films. The study highlights the importance of spin state degrees of freedom, along with thin‐film strain engineering, in creating new physical properties that do not exist in bulk materials.

Abstract Thin ferroelectric layers are capable of generating large dielectric and electromechanical responses at relatively low voltages, thus can be utilized in various applications including energy storage, energy harvesting, sensors, and actuators. Among ferroelectrics, relaxor ferroelectrics (1 − x)Pb(Mg1/3Nb2/3)O3 − xPbTiO3 are particularly interesting due to their superior dielectric and piezoelectric properties. However, dielectric and piezoelectric responses of the ferroelectric thin films are significantly suppressed relative to their bulk counterparts. The physical mechanism of the properties degradation still remains elusive, which greatly hinders their technological applications. Herein, this work systematically investigates the dielectric nonlinearity and the relationship between composition and intrinsic/extrinsic contributions of high‐quality (1 − x)Pb(Mg1/3Nb2/3)O3 − xPbTiO3 epitaxial thin films (x = 0, 0.1, 0.32) fabricated by pulsed laser deposition. Through the Rayleigh analysis, it is found that the suppression of domain wall motion by substrate clamping is the main cause of thin film performance degradation and is further confirmed by continuous application of background dc bias to extract the dielectric response's intrinsic and extrinsic contributions. This work will pave the way for practical applications of (1 − x)Pb(Mg1/3Nb2/3)O3 − xPbTiO3 thin films in energy storage and electromechanical devices.

All-inorganic CsPbI3–xBrx perovskite solar cells (PSCs) are advantageous in terms of high thermal stability, while its efficiency lags behind those of organic-inorganic hybrid perovskite counterparts. Defect passivations have been extensively applied for enhancing efficiency of all-inorganic PSCs, which are mainly based on univocal defect passivation of perovskite layer. Herein, we incorporated a bis-dimethylamino-functionalized fullerene derivative (abbreviated as PCBDMAM) as an interlayer between ZnO electron transport layer (ETL) and all-inorganic CsPbI2.25Br0.75 perovskite layer, accomplishing synchronous defect passivations of both layers and consequently dramatic enhancements of efficiency and thermal stability of PSC devices. Upon spin-coating PCBDMAM onto ZnO ETL, the surface defects of ZnO especially oxygen vacancies can be effectively passivated due to the formation of Zn−N ionic bonds. In addition, PCBDMAM incorporation affords effective passivation of PbI and IPb antisite defects within the atop perovskite layer as well via coordination bonding with Pb2+. As a result, the regular-structure planar CsPbI2.25Br0.75 PSC device delivers a champion power conversion efficiency (PCE) of 17.04%, which surpasses that of the control device (15.44%). Moreover, the PCBDMAM-incorporated PSC device maintains ~ 80% of its initial PCE after 600 h heating at 85 °C hot plate in N2 atmosphere, whereas PCE of the control device degrades rapidly to ~ 62% after 460 h heating under identical conditions. Hence, PCBDMAM incorporation benefited dramatic improvement of the thermal stability of PSC device.

Abstract Our previous studies showed that dysregulation of the long noncoding RNA (lncRNA) HOXA11-AS plays an important role in the development of glioma. However, the molecular mechanism of HOXA11-AS in glioma remains largely unknown. In this study, we explore the molecular mechanisms underlying abnormal expression and biological function of HOXA11-AS for identifying novel therapeutic targets in glioma. The expression of HOXA11-AS, and the relationship between HOXA11-AS and the prognosis of glioma patients were analyzed using databases and glioma samples. Transcriptomics, proteomics, RIP, ChIRP, luciferase, and ChIP assays were used to explore its upstream and downstream targets in glioma. The role of HOXA11-AS in regulating the sensitivity of glioma cells to reactive oxygen species (ROS) was also investigated in vitro and in vivo. We found that HOXA11-AS was significantly upregulated in glioma, and was correlated with the poor prognosis of glioma patients. Ectopic expression of HOXA11-AS promoted the proliferation, migration, and invasion of glioma cells in vitro and in vivo. Mechanistically, HOXA11-AS acted as a molecular sponge for let-7b-5p in the cytoplasm, antagonizing its ability to repress the expression of CTHRC1, which activates the β-catenin/c-Myc pathway. In addition, c-Myc was involved in HOXA11-AS dysregulation via binding to its promoter region to form a self-activating loop. HOXA11-AS, functioned as a scaffold in the nucleus, also recruited transcription factor c-Jun to the Tpl2 promoter, which activates the Tpl2-MEK1/2-ERK1/2 pathway to promote ROS resistance in glioma. Importantly, HOXA11-AS knockdown could sensitize glioma cells to ROS. Above, oncogenic HOXA11-AS upregulates CTHRC1 expression as a ceRNA by adsorbing let-7b-5p, which activates c-Myc to regulate itself transcription. HOXA11-AS knockdown promotes ROS sensitivity in glioma cells by regulating the Tpl2-MEK1/2-ERK1/2 axis, demonstrating that HOXA11-AS may be translated to increase ROS sensitivity therapeutically.

Previously, a new approach to refine α-Al grains in Al Alloys by the in-situ crystallization ZrCuAlNi metallic glasses was reported by us. A significant refining effect can be obtained, however, the effective inoculation time of ZrCuAlNi inoculant is short. Therefore, in this paper, we designed of a ZrCuAlNiLa inoculant to improve the effect inoculation time. The results showed that the effective inoculation time of ZrCuAlNiLa inoculant is prolonged obviously, which is due to La can facilitate the ZrCu compound-forming tendency and stabilize ZrCu compound phases that can act as the heterogeneous nucleation sites of α-Al phase. Meanwhile, the mechanical properties of those inoculated samples are discussed in this paper. Though this study, we provide a way to prolong the effective inoculation time of metallic glasses inoculant in Al Alloys.

Abstract Ultrashort laser pulses have been utilized to dynamically drive phase transitions in correlated quantum materials. Of particular interest is whether phases not achievable in thermal equilibrium can be induced in complex oxides with intricately coupled lattice, electron and spin degrees of freedom. Here, we tracked atomic motions in LaMnO3 following photoexcitation with MeV ultrafast electron diffraction (MeV-UED) technique. We found that the light excited state exhibits numerous signatures different from thermal equilibrium ones, including nearly conserved Bragg intensities, strongly suppressed La cation and oxygen anion displacements, and the long-range lattice orthorhombicity evolution. Furthermore, using first-principles calculations, we predict that the ferromagnetic ordering and conductivity are both enhanced upon laser excitation due to the reduction of the lattice orthorhombicity. This work benefits from recent advance in fabrication of membrane films with high epitaxial quality and in MeV-UED with large momentum space access and high temporal resolution.

Selenium (Se) plays an important role in the growth of plants. Alfalfa (Medicago sativa L.) is a perennial legume forage crop with high nutritional value and Se-rich functions. Many studies have shown that selenium can promote alfalfa growth, but few have explored the molecular biology mechanisms behind this effect. In this study, alfalfa was divided into two groups. One group was sprayed with sodium selenite (Na2SeO3) and the other group was sprayed with distilled water as a control. This study determined the growth, reproductive traits, physiological changes, transcriptome and metabolome of both groups of alfalfa. We found that foliar spraying of 100 mg/L Na2SeO3 could significantly increase the growth rate, dry weight, total Se content, amount of pollen per flower, pollen viability, pod spirals, and seed number per pod of alfalfa plants. The level of chlorophyll, soluble protein, proline, and glutathione also increased dramatically in Na2SeO3-sprayed alfalfa seedlings. After transcriptome and metabolome analysis, a total of 614 differentially expressed genes (DEGs) and 1500 differentially expressed metabolites (DEMs), including 26 secondary differentially metabolites were identified. The DEGs were mainly enriched in MAPK signaling pathway, phenylpropanoid biosynthesis, isoflavonoid biosynthesis, cutin, suberine, and wax biosynthesis, and glycerolipid metabolism. The DEMs were mainly enriched in flavone and flavonol biosynthesis, carbon metabolism, glyoxylate and dicarboxylate metabolism, nitrogen metabolism, and phenylpropanoid biosynthesis. Integrative analysis of transcriptome and metabolome showed that the foliar spraying of Na2SeO3 mainly affects phenylpropanoid biosynthesis to promote alfalfa growth.

The effects of various rolling reductions (64.7%, 72.1%, 81.4% and 88.2%) on the microstructures and mechanical behaviors of Sc-containing Al-3.2Cu-1.5Li-based alloys were experimentally investigated through XRD, SEM (equipped with EBSD), TEM and the tensile test. The results showed that the grains of hot-rolled and T6-treated alloys are mainly dominated by substructure features, and the addition of the trace Sc element can obviously impede the static and dynamic recrystallization due to the formation of fine and stable nano-Al3(Sc, Zr) particles. Additionally, the combined effects of fine grains, dispersion, substructure and precipitation strengthening make the alloys with a rolling reduction of 81.4% possess higher tensile properties. With an increase in the rolling reduction, the tensile strength of the alloys increases first and then decreases, while the elongation gradually increases and then reaches a plateau, which was ascribed to the variation in the grain size and substructure features.

The identity of catalytic sites for H2O2 generation in carbon-based materials remains controversial with limited experimental evidence to date. Here, the authors decorate various target functional groups on carbon materials and quinone-enriched samples exhibit the highest activity and selectivity.

Abstract Direct utilization of hydrocarbon fuels in solid oxide fuel cells (SOFCs) has drawn special attention for high energy conversion efficiency, low cost, and simple devices. However, when fueled with hydrocarbons, SOFCs encountered great difficulty in both performance and stability, which should be attributed to the sluggish hydrocarbon oxidizing reactions, the severe carbon deposition reactions, and the possible sulfur poisoning reactions in the anode. This review summarizes potential anode reactions in hydrocarbon-fueled SOFCs and discusses the possible anode deactivation mechanisms. Further, various strategies to improve the anode performance and stability are reviewed, including substituting alloys or increasing oxide basicity for nickel-based anodes, adopting oxide anodes, and adding catalyst layers. The advantages and challenges of each strategy are discussed. Special attention is paid on properties and models of novel oxide anodes, of which nano-metal catalysts are in-situ exsolved. The publications concerning SOFC anodes, mainly in recent 5 years, are listed and compared in this article.

Recently, there has been growing interest in using lightwave-driven scanning probe microscopy (LD-SPM) to break through the Abbe diffraction limit of focusing, yielding insight into various energy couplings and conversion processes and revealing the internal information of matter. We describe a compact and efficient optical cryostat designed for LD-SPM testing under magnetic fields. The exceptional multilayer radiation shielding insert (MRSI) forms an excellent temperature gradient when filled with heat conducting gas, which removes the requirement to install an optical window in the liquid helium cooling shell. This not only critically avoids the vibration and thermal drift caused by solid heat conduction but also minimizes light transmission loss. The application of gate valves and bellows allows a simpler and more effective replacement of the sample and working cell in the test cavity. ANSYS software is used for steady-state thermal analysis of the MRSI to obtain the temperature distribution and heat transfer rate, and the necessity of the flexible copper shielding strips is illustrated by the simulations. The topography and magnetic domain images of 45 nm-thick La0.67Ca0.33MnO3 thin films on NdGaO3(001) substrates under a magnetic field were obtained by a self-made lightwave-driven magnetic force microscope in this cryostat. The resolution and noise spectra during imaging reveal temperature stability and low vibration throughout the cryostat. The experience acquired during the development of this cryostat will help to establish cryostats of similar types for a variety of optic applications requiring the use of cryogenic temperatures.

In this work, the effects of Ce content (0.1%, 0.2%, and 0.3 wt%) on the microstructures and mechanical properties of Al-Cu-Li alloys were investigated. The results show that the grains of Al-Cu-Li alloy are refined by adding Ce element. When Ce content is less than 0.1%, the ultimate strength of the alloy increases with the increase of Ce content. However, the ultimate strength of the alloy decreases when Ce content is above 0.1%. For Al-Cu-Li alloy with different Ce content, the aging precipitation of T1 and θ′ phases play the main strengthening role. When Ce content increases from 0.1 to 0.3%, dynamic recrystallization is promoted during hot deformation. The recrystallization of the alloys is inhibited after T6 treatment with the increase of Ce content, which can be attributed to existence of the Al8Cu4Ce phases on the grain boundary. This work provides an economical and convenient method for improving the properties of Al-Cu-Li alloys by Ce addition.

The Topological Hall Effect (THE) has been considered a hallmark of magnetic skyrmions in SrRuO3 single films and heterostructures. Alternative interpretations suggest that the THE-like anomalies could also originate from multi-channel anomalous Hall effects (AHEs) induced by structural inhomogeneity. Here, we reveal another type of THE-like anomaly in SrRuO3 films that was rarely reported previously. By scanning minor loops of the Hall resistivity of ultrathin SrRuO3 films, we demonstrate that the increased saturation resistivity and reversed polarity with decreasing a scanning field cannot be explained by THE, while it shows consistence with spatially inhomogeneous AHE. Our research provides a simple but effective way to quantitatively distinguish between THE and inhomogeneous AHE in those magnetic systems even beyond SrRuO3.

Ultrathin porous Co3O4 nanosheets are synthesized successfully, the thickness of which is about three unit-cell dimensions. The enhanced oxygen evolution reaction (OER) performance and electronic interaction between Co3O4 and Au is firstly reported in Co3O4 ultrathin porous nanosheets by physically mixing with Au nanoparticles. With the loading of the Au nanoparticles, the current density of ultrathin porous Co3O4 nanosheets is enhanced from 9.97 to 14.76 mA cm−2 at an overpotential of 0.5 V, and the overpotential required for 10 mA cm−2 decreases from 0.51 to 0.46 V, smaller than that of commercial IrO2 (0.54 V). Furthermore, a smaller Tafel slope and excellent durability are also obtained. Raman spectra, XPS measurement, and X-ray absorption near edge structure spectra (XANES) show that the enhanced OER ascribed to a higher Co2+/Co3+ ratio and quicker charge transfer due to the electronic interaction between Au and ultrathin Co3O4 nanosheets with low-coordinated surface, and Co2+ ions are beneficial for the formation of CoOOH active sites.

Hydrogen adsorption/desorption behavior plays a key role in hydrogen evolution reaction catalysis. Here, the authors demonstrate the rational balancing of hydrogen adsorption/desorption by orbital modulation for significantly enhanced hydrogen evolution performance.

Identification of active sites is one of the main obstacles to rational design of catalysts for scientific and industrial applications. Here, the authors demonstrate the synthesis and structural identification of Zn based active sites, as well as the related structural activation for oxygen species.

While splitting water into fuel may provide a green, renewable method for energy storage, water oxidation is its bottleneck. Here, authors reported multiferroic electrocatalysts with improved oxygen evolution performances assisted by polarization.

The filtering and polarizing of terahertz waves are essential for various terahertz applications. Here, we use two-dimensional (2-D) rectangular subwavelength hole arrays (SHAs) to achieve efficient wave filtering and polarizing in the terahertz region. The transmissive filtering is obtained by exciting the specified resonant modes within the subwavelength holes. With the same basic physics, the elliptic-to-linear and linear-to-elliptic (linear-to-circular) polarization conversions are successfully achieved by properly arranging the 2-D SHAs. Thanks to its easy realizability, these 2-D SHAs can promisingly be developed as efficient terahertz wave filters and polarizers for practices.

We demonstrate a broadband and polarization selective terahertz modulator with ultrafast modulation speed, based on the Si grating metasurface on the Sapphire substrate. The Si layer is implanted with B+ and subsequently annealed, which significantly reduces the lifetime of carriers and increases the carrier density, and thus realizes ultrafast and efficient modulation. Our modulator achieves modulation depth up to 60% for the x-polarized THz wave and less than 1% for the y-polarized THz wave in the frequency ranging from 0.5 to 2.5 THz, with switch-on and switch-off time of modulation in 20 ps and around 300 ps, respectively. The carrier dynamics of the fabricated Si grating is also studied to illustrate the ultrafast modulated mechanism. Our results pave the way for ultrafast manipulation of terahertz spectrum and shows great potential in terahertz communication.

Electric field controlled magnetism provides an energy efficient way for the operations in the spintronic devices. Here the authors show strain induced, reversible, nonvolatile electric field control of magnetization and magnetoresistance in a magnetic tunnel junction on a ferroelectric substrate at room temperature and zero magnetic field.

Abstract Low‐temperature solution‐processed TiO2 nanocrystals (LT‐TiO2) have been extensively applied as electron transport layer (ETL) of perovskite solar cells (PSCs). However, the low electron mobility, high density of electronic trap states, and considerable photocatalytic activity of TiO2 result in undesirable charge recombination at the ETL/perovskite interface and notorious instability of PSCs under ultraviolet (UV) light. Herein, LT‐TiO2 nanocrystals are in situ fluorinated via a simple nonhydrolytic method, affording formation of Ti─F bonds, and consequently increase electron mobility, decrease density of electronic trap states, and inhibit photocatalytic activity. Upon applying fluorinated TiO2 nanocrystals (F‐TiO2) as ETL, regular‐structure planar heterojunction PSC (PHJ‐PSC) achieves a champion power conversion efficiency (PCE) of 22.68%, which is among the highest PCEs for PHJ‐PSCs based on LT‐TiO2 ETLs. Flexible PHJ‐PSC devices based on F‐TiO2 ETL exhibit the best PCE of 18.26%, which is the highest value for TiO2‐based flexible devices. The bonded F atoms on the surface of TiO2 promote the formation of Pb─F bonds and hydrogen bonds between F− and FA/MA organic cations, reinforcing interface binding of perovskite layer with TiO2 ETL. This contributes to effective passivation of the surface trap states of perovskite film, resulting in enhancements of device efficiency and stability especially under UV light.

GBM (Glioblastoma multiform) is the most malignant tumor type of the central nervous system and has poor diagnostic and clinical outcomes. LncRNAs (Long non-coding RNAs) have been reported to participate in multiple biological and pathological processes, but their underlying mechanism remains poorly understood. Here, we aimed to explore the role of the lncRNA HAS2-AS1 (HAS2 antisense RNA 1) in GBM. GSE103227 was analyzed, and qRT-PCR was performed to measure the expression of HAS2-AS1 in GBM. FISH (Fluorescence in situ hybridization) was performed to verify the localization of HAS2-AS1. The interaction between HAS2-AS1 and miR-137 (microRNA-137) was predicted by LncBook and miRcode followed by dual‐luciferase reporter assays, and the relationships among HAS2-AS1, miR-137 and LSD1 (lysine-specific demethylase 1) were assessed by WB (western blot) and qRT-PCR. Colony formation and CCK-8 (cell counting kit-8) assays were performed as functional tests. In vivo, nude mice were used to confirm the function of HAS2-AS1. HAS2-AS1 expression was upregulated in GBM cell lines, and HAS2-AS1 was localized mainly in the cytoplasm. In vitro, high HAS2-AS1 expression promoted proliferation, and knockdown of HAS2-AS1 significantly inhibited proliferation. Furthermore, HAS2-AS1 functioned as a ceRNA (competing endogenous RNA) of miR-137, leading to the disinhibition of its downstream target LSD1. The miR-137 level was downregulated by HAS2-AS1 overexpression and upregulated by HAS2-AS1 knockdown. In a subsequent study, LSD1 expression was negatively regulated by miR-137, while miR-137 reversed the LSD1 expression levels caused by HAS2-AS1. These results were further supported by the nude mouse tumorigenesis experiment; compared with xenografts with high HAS2-AS1 expression, the group with low levels of HAS2-AS1 exhibited suppressed proliferation and better survival. We conclude that lncRNA HAS2-AS1 promotes proliferation by functioning as a miR‐137 decoy to increase LSD1 levels and thus might be a possible biomarker for GBM.

Abstract The participation of lattice oxygen in the oxygen evolution reaction (OER) process has been proved to be faster in kinetics than the mechanisms where only metal is involved, although activating the lattice oxygen in the traditional rigid structures remains a big challenge. In this work, efforts are devoted to exploring a new flexible structure that is competent in providing large amounts of oxygen vacancies as well as offering the freedom to manipulate the electronic structure of metal cations. This is demonstrated by anchoring low valence state Co at high valence state Nb sites in the tetragonal tungsten bronze (TTB)‐structured Sr0.5Ba0.5Nb2‐xCoxO6‐δ, with different ratios of Co to Nb to optimize the Co substitution proportion. It is found that the occupation of Co in the Nb5+ sites gives rise to the generation of massive surface oxygen vacancies (Ovac), while Co itself is stabilized in Co2+ by adjacent Ovac. The coexistence of Ovac and LS Co2+ enables an oxygen intercalation mechanism in the optimal SBNC45 with specific activity at 1.7 V versus reversible hydrogen electrode that is 20 times higher than for the commercial IrO2. This work illuminates an entirely new avenue to rationally design OER electrocatalysts with ultrafast kinetics.

Few-layered black phosphorus has unique and appealing electronic properties but is easily oxidized in air. Here, the authors covalently functionalize black phosphorus nanosheets with C60 at their edges, providing improved stability and enhanced photoelectrochemical and photocatalytic activities.

Synergistic effect of band convergence and resonant level could be manipulated in SnTe by co-doping In and Hg, leading to a potential thermoelectric performance enhancement in a much wider temperature range. In this work we carefully investigated thermoelectric properties of the In-Hg co-doped SnTe, synthesized by a hot pressing method. With this co-doping the Seebeck coefficients of the co-doped samples were greatly improved (over 50 μVK−1) at the room temperature. Although power factors of the In-Hg co-doped SnTe were also able to be optimized, the peak ZT (0.9 at 850 K in Sn0.98Bi0.02Te-1%HgInTe2), however, is not high enough when comparing to other co-doped SnTe systems. This may be caused by the relatively high lattice thermal conductivity. An apparent competition between band convergence doping and resonant level doping was observed in our experiment. The results suggest that band engineering via co-doping should be further understood in order to optimize the thermoelectric properties inside the material system.

Hydrogenation is an effective way to tune the property of metal oxides. Here, the authors report a simple approach to hydrogenate VO2 in acid solution under ambient conditions by placing a small piece of low workfunction metal on VO2 surface.

Dynamic phase modulation is vital for tuneable focusing, beaming, polarisation conversion and holography. However, it remains challenging to achieve full 360° dynamic phase modulation while maintaining high reflectance or transmittance based on metamaterials or metasurfaces in the terahertz regime. Here, we propose a doubly resonant graphene–metal hybrid metasurface to address this challenge. Simulation results show that by varying the graphene Fermi energy, the proposed metasurface with two shifting resonances is capable of providing dynamic phase modulation covering a range of 361° while maintaining relatively high reflectance above 20% at 1.05 THz. Based on the phase profile design, dynamically tuneable beam steering and focusing were numerically demonstrated. We expect that this work will advance the engineering of graphene metasurfaces for the dynamic manipulation of terahertz waves.