摘要：Delivering excellent carrier separation through ferroelectric polarization is desirable to achieve effective solar hydrogen ***,Bi_(0.9)Dy_(0.1)FeO_(3)/g-C_(3)N_(4)(BDFO/GCN)Z-scheme photocatalyst was constructed by loading BDFO nanoparticles onto sheet-like GCN,in which BiFeO_(3)(BFO)was doped with the rare-earth element Dy to narrow the optical bandgap and enhance the ferroelectric *** polarization effectively promoted the separation and transport of photo-generated carriers in BFO,and the Z-scheme exhibited stable reaction activity during photocatalytic degradation and photocatalytic hydrogen *** electric polarization,the heterojunction photocatalyst achieves 100%degradation of Rhodamine B(RhB)under simulated *** evolution rate of hydrogen was improved from approximately 742.5 to 1084.0μmol·g^(−1)·h^(−1)after *** remarkable activity is attributed to the improved carrier separation facilitated by the internal polarization *** work offers novel insights into the rational design of efficient ferroelectric photocatalysts.

摘要：Artificial neural networks have dramatically improved the performance of many machine-learning applications such as image recognition and natural language processing. However, the electronic hardware implementations of the above-mentioned tasks are facing performance ceiling because Moore’s Law is slowing down. In this article, we propose an optical neural network architecture based on optical scattering units to implement deep learning tasks with fast speed, low power consumption and small *** optical scattering units allow light to scatter back and forward within a small region and can be optimized through an inverse design method. The optical scattering units can implement high-precision stochastic matrix multiplication with mean squared error < 10-4 and a mere 4*4 um2 ***, an optical neural network framework based on optical scattering units is constructed by introducing "Kernel Matrix", which can achieve 97.1% accuracy on the classic image classification dataset MNIST.

摘要：理解铁电材料畴结构在低温条件下的翻转行为,对于铁电物理以及其在宽温域的应用都非常重要;然而,目前在低温条件下直接观测介观尺度下的畴翻转仍然面临着巨大的挑战.本论文利用铁酸铋(BiFeO_(3))作为模型来研究3.6–260 K温度范围内的铁电畴翻转行为.菱形相的BiFeO_(3)在温度为130 K时观测到了明显的铁电保持失效现象;这是因为BiFeO_(3)在130 K附近有较大的热释电系数,从而使其升温到该温度附近时释放了大量的热释电电荷,进而产生较强的退极化场,导致铁电极化翻转.另外,本论文还发现通过纳米尺度设计相界可以有效地抑制铁电保持失效.本研究为变温条件下,尤其是低温温域,研究铁电翻转提供了实验范式.

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：Catalytic hydrogenation is a vital industrial means to produce value-added fuels and fine chemicals,however, requiring highly efficient catalysts, especially the nonprecious ones. To date, the majority of high-performance industrial hydrogenation catalysts are made of precious metals-based materials, and any given catalyst could only be used to catalyze one or few specific reactions. Herein, we exemplify a crystal phase engineering approach to empower Ni nanoparticles(NPs) with superb intrinsic catalytic activities toward a wide spectrum of hydrogenation reactions. A facile pyrolysis approach is used to directly convert a Ni-imidazole MOF precursor into hexagonal close-packed(hcp)-phased Ni NPs on carbon support. The as-synthesized hcp-phased Ni NPs exhibit unprecedented hydrogenation catalytic activities in pure water towards nitro-, aldehyde-, ketone-, alkene-and N heterocyclic-compounds, outperforming the face-centered cubic(fcc)-Ni counterpart and the reported transition metalsbased catalysts. The density functional theory calculations unveil that the presence of hcp-Ni boosts the intrinsic catalytic hydrogenation activity by coherently enhancing the substrate adsorption strength and lowering the reaction barrier energy of the rate-determining step. We anticipate that the crystal phase engineering design approach unveiled in this work would be adoptable to other types of reactions.

摘要：由于C=C双键交联反应机制的成熟,金属氧化物光刻胶得到了广泛的发展.然而,由于不稳定的C=C双键,这种材料需要低温和遮光存储.在此,首次在金属氧簇中提出了C-F键交联策略用于光刻图案化.以光刻胶Zn-TBA为例,它形成光滑无缺陷的薄膜,且表面粗糙度Rq小于0.2 nm.使用极紫外(EUV)干涉掩模,在65 mJ cm^(-2)曝光剂量下形成37.5 nm的半周期(HP)图案.在EUV曝光和正己烷显影后,通过原子力显微镜(AFM)观察到负性光刻胶形貌.重要的是,Zn-TBA可以在室温和明亮的环境中储存.除了脱羧之外,我们还提出光引发的C-F交联是Zn-TBA图案的主要贡献者,并通过高分辨率X射线光电子能谱(HRXPS)和密度泛函理论(DFT)计算得以证明.这种新颖的光刻机制为下一代金属基材料的设计提供了新的思路.

摘要：Two-dimensional （2D） materials have attracted growing attention since the discovery of graphene [1]. Transition metal dichalcogenide （TMD） semiconductors, such as MoS2 and WS2, became popular materials in recent years, because they usually have intrinsic bandgaps and an in- direct-to-direct bandgap transition from bulk to mono- layer limit [2-6]. Although graphene and TMDs are promising materials in field-effect devices [7-9], their heterostructures are more advanced in charge-splitting functions for the applications in optoelectronic devices [10-15].

摘要：Negative thermal expansion(NTE),as an abnormal physical behavior,has been followed by scientists’attention over the past 30 years,due to its fascinating physical mechanisms and the prospect of high-precision thermal expansion control[1-5].Although some NTE materials(alloys[6],cyanides[7],fluorides[8-10],nitrides[11],oxides[12,13],MOFs[14-16],etc.)have been found,their number and variety are still very small,limiting their *** and designing new NTE materials is an important and challenging topic for the development of the field of *** have been continually reviewing and summarizing obtained results to look to the future of NTE[17-23].

摘要：聚合物基固态电解质得益于其易加工性,最有希望应用于下一代固态锂金属电池.目前,聚合物基态电解质的离子电导率提升策略多为加入导锂陶瓷以构建离子传输通道,其提升程度有限.电场在锂离子输运过程中存在重要影响,目前研究中有关电场对锂离子传输的影响机制尚不明确.本文将兼具高离子电导率和高介电常数的铌酸锂嵌入聚偏氟乙烯基体中,设计了一种新型复合固态电解质.铌酸锂颗粒有效调节电解质内部电场结构,增强了离子输运方向电场强度,实现了离子电导率的大幅提升(7.39×10^(-4)S cm^(-1),25℃).该电解质匹配高镍正极和锂金属负极的固态电池可稳定循环1000次以上,容量保持率为72%.该研究为设计下一代固态锂电池用高离子电导复合固态电解质提供了新的策略.

摘要：Development of efficient heterostructured photocatalysts that respond to visible light remains a considerable *** herein show the synthesis of ZnIn2S4/carbon quantum dot hybrid photocatalysts with flowerlike microspheres via a facile solvothermal *** ZnIn2S4/carbon quantum dot flowerlike microspheres display enhanced photocatalytic and photoelectrochemical activity compared with that of pure *** a content of only 0.5 wt%carbon quantum dots,93%of Cr(VI)is reduced under visible‐light irradiation at 40 *** a co‐catalyst,the carbon quantum dots improve the light absorption and lengthen the lifetime of charge carriers,consequently enhancing the photocatalytic and photoelectrochemical activity.