摘要：Synchrotron radiation-based micro-Laue technique has showcased great application potentials in materials science study for its unprecedented crystal orientation and lattice strain/stress *** we report the updated progress in the development of the micro-Laue technique on the X-ray test beamline at Shanghai Synchrotron Radiation *** far,40μm(h)×50μm(v)X-ray beam spot is routinely obtained,with the convergent angle of 0.2 mrad(h)×0.12 mrad(v).Area scans are conducted on a GH3535 Nibased superalloy base metal and weld joint with the same chemical *** analyzing the tremendous amount of Laue diffraction patterns using in-house developed software packages,the crystal orientation,elastic strain,and defect distributions are mapped and *** a successful proof-of-principle study offers first-hand experience on the further optimization of the design and construction of the scanning micro-Laue facility on the superbend beamline with improved spatial resolution and multiple functions for simultaneous chemical fluorescence mapping and in-situ microstructural evolution *** micro-Laue diffraction beamline at Shanghai Synchrotron Radiation Facility will provide a versatile and powerful tool for the orientation and strain/stress mapping combined with phase identification with micron-sized spatial resolution.

摘要：The design and construction of highly effective circularly polarized luminescence(CPL)-active materials has aroused considerable attention due to their widespread applications in sensors,optical devices,and asymmetric ***,the exploration of novel CPL-active materials with high luminescence dissymmetry factor(glum)values is still a ***,we describe a new approach for the preparation of supramolecular metallacycles with amplified CPL promoted by hierarchical self-assembly involving Pt···Pt ***,the resultant metallacycles exhibited strong CPL signals with high glum values,while their corresponding precursors were CPL *** CPL amplification mechanism was comprehensively validated by ultravioletvisible absorption,emission spectroscopy,nuclear magnetic resonance spectroscopy,scanning electron microscopy,transmission electron microscopy,atomic force microscopy,coarse-grained molecular dynamics simulations,and timedependent density functional theory *** work thus provides the first example of preparing highly effective CPL-active materials based on hierarchical self-assembly involving Pt···Pt interactions.

摘要：Perovskite solar cells(pero-SCs)performance is essentially limited by severe non-radiative losses and ion *** numerous strategies have been proposed,challenges remain in the basic understanding of their ***,we report a dielectric-screening-enhancement effect for perovskite defects by using organic semiconductors with finely tuned molecular structures from the atoms *** method produced various perovskite films with high dielectric constant values,reduced charge capture regions,suppressed ion migration,and it provides an efficient charge transport pathway for suppressing non-radiative recombination beyond the passivation *** resulting pero-SCs showed a promising power conversion efficiency(PCE)of 23.35%with a high open-circuit voltage(1.22 V);and the 1-cm^(2) pero-SCs maintained an excellent PCE(21.93%),showing feasibility for scalable *** robust operational and thermal stabilities revealed that this method paved a new way to understand the degradation mechanism of pero-SCs,promoting the efficiency,stability and scaled fabrication of the pero-SCs.

摘要：Two-dimensional layered double hydroxides(LDHs)have been identified as promising electrocatalysts for the oxygen evolution reaction(OER);however,the simple and effective synthesis of high-quality LDHs remains extremely challenging and the active sites have not been ***,we report a facile solution-reaction method for preparing an ultrathin(thickness<2 nm)nonprecious CoFe-based ***_(1)Fe_(0.2) LDH delivers a current density of 10 mA cm^(-2) and a high turnover frequency of 0.082 s^(-1) per total 3d metal atoms at a low overpotential of 256 *** mass activity is 277.9 A g^(-1) at an overpotential of 300 mV for the *** studies reveal the Co site as the main active center for the *** doped Fe lowers the reaction barrier by accelerating the charge-transfer *** calculations reveal that the surface Co sites adjacent to Fe atoms are the active centers for the OER and the subsurface Fe dopants excessively weaken the OH^(*)adsorption,thus increasing the energy barrier of the rate-determining *** study can guide the rational design of high-performance CoFe-based LDHs for water splitting.

摘要：The typical Haber technical process for industrial NH_(3)production involves plenty of energy-consumption and large quantities of greenhouse gas *** contrast,electrochemical N_(2)reduction proffers environment-friendly and energy-efficient avenues to synthesize NH_(3)at mild conditions but demands efficient electrocatalysts for the N_(2)reduction reaction(NRR).Herein we report for the first time that commercial indium-tin oxide glass(ITO/G)can be used as a catalyst electrode toward artificial N_(2)fixation,as it demonstrates excellent selectivity at mild *** ITO/G delivers excellent NRR performance with a NH_(3)yield of 1.06×10^(-10) mol s^(-1) cm^(-2) and a faradaic efficiency of 6.17%at-0.40 V versus the reversible hydrogen electrode(RHE)in 0.5 M ***,the ITO/G also possesses good electrochemical stability and ***,the possible reaction mechanism for the NRR on the ITO catalysts was explored using first-principles calculations.

摘要：The catalytic effect of electrode materials is one of the most crucial factors for achieving efficient electrochemical energy conversion and ***-based metal composites were widely synthesized and employed as electrode materials because of their inherited outstanding ***,electrode materials can provide a higher capacity than the anticipated values,even beyond the theoretical *** origin of the extra capacity has not yet been explained accurately,and its formation mechanism is still ***,we first summarized the current research progress and drawbacks in energy storage devices(ESDs),and elaborated the role of catalytic effect in enhancing the performance of ESDs as follows:promoting the evolution of the solid electrolyte interphase(SEI),accelerating the reversible conversion of discharge/charge products,and improving the conversion speed of the intermediate and the utilization rate of the active materials,thereby avoiding the shuttling ***,a particular focus was placed on the interaction between the catalytic effect and energy storage performance in order to highlight the efficacy and role of the catalytic *** hope that this review could provide innovative ideas for designing the electrode materials with an efficient catalytic effect for ESDs to promote the development of this research field.

摘要：具有高发光性能的二维材料被认为是实现光电器件应用的极具前途的材料.其中,硒化铟(InSe)是一种具有代表性的二维材料,近些年在光电领域表现出巨大的应用潜力,因此吸引了研究者们的广泛关注.然而,InSe的光-物质相互作用极其微弱,因为其带隙激子的偏振取向是面外的,主要被面外偏振光激发而对正常入射光(面内偏振)的响应极其微弱,这大大限制了其在光电器件中的实际应用.在此,我们提出了一种方法,即通过将少层InSe转移到Ag纳米棱镜阵列上,显著提升InSe在线性和非线性体系的光学响应.结合实验分析,增强的机理主要来自于两种机制的协同作用:一方面,局域表面等离子体共振产生的局部强化电磁场垂直分布于金属表面,与面外偏振的InSe带隙激子发生高效耦合,增强了InSe的光-物质相互作用;另一方面,独特设计的弯曲结构增加了入射光在平面外的偏振分量,促使InSe面外激子对光的吸收和散射效率增强.通过进一步调整InSe的厚度,我们实现了光致发光和二次谐波信号的两个数量级的增强.因此,我们的工作为改善InSe的光学特性提供了一个有效的途径,使其在光电器件的实际应用中迈出了重要的一步.

摘要：本文研究了一种新型低密度(~6.24 g cm^(-3))双相AlTiVCoNi高熵合金,其组织结构由有序L21高熵金属间化合物、无序体心立方结构和纳米L21相多层次结构构成.该合金在1200℃+24 h热处理下未发生相结构转变,在此条件下具有优异的高温相结构稳定性,其铸态和热处理态的压缩屈服强度相当,达到~1.6 GPa.另外,该合金在室温和600℃条件下表现出了优异的强塑性匹配和优异的比屈服强度,分别达到了约261和210 MPa g^(-1)cm^(3).该合金的超高强度主要源于有序L21相与体心立方相的半共格界面导致的一种强相结构稳定性和多层次结构的复合强化机制.该合金在800和1000℃压缩过程中出现了动态再结晶软化,使得其高温强度有所降低.这种“具有半共格界面L21+体心立方+纳米L21颗粒”的多层次结构设计为开发新型低密度耐高温高熵合金提供了一种新设计思路.

摘要：Cholesteric liquid crystal(CLC)particles can adaptively respond to constant changes in external stimuli and thus are widely used in solvent-sensing,pattern fabrication,and *** studies discussed the color change at the center of the particles for various ***,few studies analyzed the color change of the brush structure of particles in response to various applications because of the complicated birefringence *** this paper,we present a novel integrated sensing system based on the synergetic color change from the center and the brush structure of CLC *** system provides abundant and additional sensing information relative to the traditional *** particles are prepared by mixing reactive mesogens,a reactive chiral dopant,a non-reactive LC molecule,and a photoinitiator by using a microfluidic device and subsequent *** CLC particles exhibit gorgeous color at the center and brush structure upon various solvent stimuli because of the Bragg reflection and the birefringence effect,which is explained by the possible color-changing mechanism introduced in this *** proof-of-concept applications,such color-changing polymer particles are demonstrated in multi-solvent-sensing detection and pattern *** study provides new insights into the development of stimuli-responsive advanced functional materials with tailorable nanostructures toward technological applications ranging from sensing to display.

摘要：本文设计合成了两种具有不同连接方式(亚胺键和sp^(2)-C-CN键)的三嗪基共价有机框架(COFs)材料.连接单元的微小变化导致可见光驱动制氢性能的巨大差异.具有sp^(2)碳连接方式的全π共轭二维COFs在450 nm波长处表现出13.48%的外量子效率,优于已报道的COFs光催化剂.而亚胺键的二维COFs几乎没有光活性.借助光电化学研究和量子化学计算进一步研究了二维COFs的催化机理,为太阳能转化高性能有机光催化剂的制备提供了新的见解.