摘要：Photoelectrochemical(PEC)water splitting for solar energy conversion into chemical fuels has attracted intense research *** semiconductor hematite(α-Fe_(2)O_(3)),with its earth abundance,chemical stability,and efficient light harvesting,stands out as a promising photoanode ***,its electron affinity is too deep for overall water splitting,requiring additional *** engineering has been used to reduce the onset potential of hematite *** we focus instead on energy band engineering hematite by shrinking the crystal lattice,and the water-splitting onset potential can be decreased from 1.14 to 0.61 V *** reversible hydrogen *** is the lowest record reported for a pristine hematite photoanode without surface modification.X-ray absorption spectroscopy and magnetic properties suggest the redistribution of 3d electrons in the as-synthesized grey hematite *** function theory studies herein show that the smaller-lattice-constant hematite benefits from raised energy bands,which accounts for the reduced onset potential.

摘要：Early detection of cancer biomarkers applied in real-time disease diagnosis and therapies can increase the survival rate of *** tumor DNA(ct DNA)as a typical cancer biomarker plays a great role in the process of tumor disease monitoring,especially in early ***,most ct DNA detection systems have not been widely used due to their low sensitivity,poor specificity,and high ***,we developed an alternative ct DNA detection system to present the levels of ct DNA by recording the fluorescence signals of the system containing upconversion nanoparticles(UCNPs),Fe_(3)O_(4),and entropy-driven strand displacement *** method has a practical sensitivity with a wide linear range from 100 amol L^(-1)to 1 nmol L^(-1)and a low detection limit of 1.6 amol L^(-1).Furthermore,the system demonstrates a practical application in mouse blood serum samples and meets the requirements for rapid,sensitive,specific,and economical diagnosis of ***,this ct DNA detection system may have great potential for ct DNAdetection and clinical diagnosis.

摘要：Highly active and low-cost catalysts for electrochemical reactions such as the hydrogen evolution reaction （HER） are crucial for the development of efficient energy conversion and storage technologies. Theoretical simulations have been instrumental in revealing the correlations between the electronic structure of materials and their catalytic activity, and guide the prediction and development of improved catalysts. However, difficulties in accurately engineering the desired atomic sites lead to challenges in making direct comparisons between experi- mental and theoretical results. In MoS2, the Mo-edge has been demonstrated to be active for HER whereas the S-edge is inert. Using a computational descriptor- based approach, we predict that by incorporating transition metal atoms （Fe, Co, Ni, or Cu） the S-edge site should also become HER active. Vertically standing, edge-terminated MoS2 nanofilms provide a well-defined model system for verifying these predictions. The transition metal doped MoS2 nanofilms show an increase in exchange current densities by at least two-fold, in agreement with the theoretical calculations. This work opens up further opportunities for improving electrochemical catalysts by incorporating promoters into particular atomic sites, and for using well-defined systems in order to understand the origin of the promotion effects.

摘要：As the base of modern electronic industry,field-effect transistor(FET) requires the channel material to have both moderate bandgap and high mobility. The recent progresses indicate that few-layer black phosphorus has suitable bandgap and higher mobility than two-dimensional(2D) MoS_2, but the experimentally achieved maximal mobility(1000 cm^2 V^(-1) s^(-1)) is still obviously lower than those of classical semiconductors(1,400 and 5,400 cm^2 V^(-1) s^(-1) for Si and InP). Here, for the first time, we report on monolayer antimonide phosphorus(SbP) as a promising 2D channel material with suitable direct bandgap, which can satisfy the on/off ratio, and with mobility as high as 10~4 cm^2 V^(-1) s^(-1)based on density functional theory calculation. In particular,α-Sb_(1-x)P_x monolayers possess 0.3–1.6 eV bandgaps when0.1 ≤ x ≤ 1, which are greater than the minimum bandgap(0.4 eV) required for large on/off ratio of FET. Surprisingly,the carrier mobilities of α-Sb_(1-x)P_x monolayers exhibit very high upper limit approaching 2×10~4 cm^2 V^(-1) s^(-1) when 0 ≤x ≤ 0.25 due to the ultra-small effective mass of holes and electrons. This work reveals that 2D SbP with both suitable bandgap and high mobility could be a promising candidate as eco-friendly high-performance FET channel materials avoiding short-channel effect in the post-silicon era, especially when considering the recent experimental success in realizing arsenide phosphorus(AsP) with similar structure.

摘要：我们设计并制备了一种基于LiGa_(4)(MgGe)_(0.5)O_(8):Cr荧光粉变温发光特性的柔性温度传感光纤.通常来说,随着温度的升高,发光材料基质的电子-声子作用将加剧,这会导致其发射峰的半高宽(FWHM)在升温时不断加宽.在本工作中,随着LiGa_(5-x)(MgGe)_(x)O_(8):Cr中[Mg^(2+)-Ge^(4+)]化学单元成分比例的增加,荧光粉近红外发光的FWHM出现明显展宽,其外量子效率也从24.8%增加到50.0%.进一步研究发现,LiGa_(4)-(MgGe)_(0.5)O_(8):Cr纳米荧光粉的发光具有优异的热稳定性和温度传感特性,在443 K时绝对灵敏度可达7.51 cm^(-1)K^(-1),303 K下相对灵敏度为0.64%K^(-1).基于此,我们搭建了具有可重复性、高精度和优异稳定性的柔性全光纤系统,并将其用于实时监测物体的温度.本研究不仅探索了具有锐线发射的Cr^(3+)掺杂发光材料的应用,而且丰富了基于荧光材料带宽特性的光学测温新思路.

摘要：Theranostic nanoprobes can potentially integrate imaging and therapeutic capabilities into a single platform,offering a new personalized cancer diagnostic ***,there is a growing concern that their clinical application is not safe,particularly due to metal-containing elements,such as the gadolinium used in magnetic resonance imaging(MRI).We demonstrate for the first time that the photothermal melting of the DNA duplex helix was a reliable and versatile strategy that enables the on-demand degradation of the gadolinium-containing MRI reporter gene from polydopamine(PDA)-based theranostic *** combination of chemotherapy(doxorubicin)and photothermal therapy,which leads to the enhanced anti-tumor *** vivo MRI tracking reveals that renal filtration was able to rapidly clear the free gadolinium-containing MRI reporter from the mice *** results in a decrease in the long-term toxic effect of theranostic MRI *** findings may pave the way to address toxicity issues of the theranostic nanoprobes.

摘要：A facile strategy was designed for the fabrication of Fe3O4-nanoparticle- decorated TiO2 nanofiber hierarchical heterostructures （FTHs） by combining the versatility of the electrospinning technique and the hydrothermal growth method. The hierarchical architecture of Fe3O4 nanoparticles decorated on TiO2 nanofibers enables the successful integration of the binary composite into batteries to address structural stability and low capacity. In the resulting unique architecture of FTHs, the 1D heterostructures relieve the strain caused by severe volume changes of Fe3O4 during numerous charge-discharge cycles, and thus suppress the degradation of the electrode material. As a result, FTHs show excellent performance including higher reversible capacity, excellent cycle life, and good rate performance over a wide temperature range owing to the synergistic effect of the binary composition of TiO2 and Fe304 and the unique features of the hierarchical nanofibers.

摘要：Two-dimensional(2D) lead halide perovskite materials are emerging as one of promising light-absorbing materials in perovskite solar cells(PSCs), which show outstanding stability and defect passivation. Unfortunately, the power conversion efficiency(PCE) of those stable 2D PSCs is still far behind that of 3D PSCs. Herein, we reported a simple in-situ growth technique for the ethylenediamine lead iodide(EDAPbI4) layer on the top of formamidinium lead iodide(FAPbI3) layer. The rationally designed layered architecture of2D-3 D perovskite film could improve the PCE of the PSCs. In addition, benefiting from the high moisture resistance and inhibited ion migration of EDAPbI4 layer, the 2D-3D-based devices showed obviously enhanced long-term stability,keeping the initial PCE value for 200 h and 90% of its initial PCE even after 500 h.

摘要：Anchoring molecular cocatalysts on semiconductors has been recognized as a general strategy to boost the charge separation efficiency required for efficient ***,the effect of molecular cocatalysts on energy funneling(i.e.,directional energy transfer)inside semiconductor photocatalysts has not been demonstrated *** we prepared CdS nanorods with both thin and thick rods and anchored the conjugated molecules 2‐mercaptobenzimidazole(MBI)and cobalt molecular catalysts(MCoA)sequentially onto the surface of *** absorption measurements revealed that MBI molecules facilitated energy funneling from thin to thick rods by the electronic coupling between thin and thick nanorods,which is essentially a light‐harvesting antenna approach to enhance the charge generation efficiency in the reaction center(here the thick rods).Moreover,MBI and MCoA molecules selectively extracted photogenerated holes and electrons of CdS nanorods rapidly,leading to efficient charge ***,CdS/MBI/MCoA displayed 15 times enhanced photocatalytic H_(2) evolution(1.65 mL)than pure CdS(0.11 mL)over 3 h of *** amount of H_(2) evolution reached 60 mL over 48 h of illumination with a high turnover number of 26294 and an apparent quantum efficiency of 71%at 420 *** study demonstrates a novel design principle for next‐generation photocatalysts.

摘要：The development of high-performance solid polymer electrolytes is crucial for producing all-solid-state lithium metal batteries with high safety and high energy ***,the low ionic conductivity of solid polymer electrolytes and their unstable electrolyte/electrode interfaces have hindered their widespread *** address these critical challenges,a strong Lewis acid(aluminum fluoride(AIF_(3)))with dual functionality is introduced into poly(ethylene oxide)(PEO)-based polymer *** AlF;facilitates the dissociation of lithium salt,increasing the iontransfer efficiency due to the Lewis acid-base interaction;further the in-situ formation of lithium fluoride-rich interfacial layer is promoted,which suppresses the uneven lithium deposition and continuous undesired reactions between the Li metal and PEO *** from our rational design,the symmetric Li/Li battery with the modified electrolyte exhibits much longer cycling stability(over 3600 h)than that of the pure PEO/lithium bis(trifluoromethanesulfonyl)imide(LiTFSI)electrolyte(550 h).Furthermore,the all-solid-state LiFeP04 full cell with the composite electrolyte displays a much higher Coulombic efficiency(98.4%after 150 cycles)than that of the electrolyte without the AlF;additive(63.3%after 150 cycles)at a large voltage window of 2.4-4.2 V,demonstrating the improved interface and cycling stability of solid polymer lithium metal batteries.