Er:ZBLAN玻璃的一光束上转换立体显示的初步研究

本文研究了一光束上转换三维立体显示 ,所用材料为Er:ZBLAN氟化物玻璃 ;利用 96 6nm的连续波半导体激光研究了一光束上转换三维立体显示的尺寸效应 ,且得到了它的上转换发光谱 ;尤其是发现了基于 15 2 0nm的半导体激光激发的多光子上转换一光束三维立体显示的性能有大幅度提高 ,这在国际上还未见报道。     

聚氨酯／聚（苯乙烯—甲基丙烯酸甲酯—甲基丙烯酸互穿聚合物网络的研究

研究了聚氨酯／聚互穿合笺网络，动态力学性能及透射电镜结果均表明该体系相分离较严重。ＩＮＰ具有两个玻璃化转变温度，它们有不同程度的内移，形成一定程度分子水平的混合。而ＩＰＮ（５０／５０）其分子混合水平较大，互穿缠结程度较高。     

气相色谱-常压微波等离子体发射光谱系统操作参数的考察及最优化

本文对影响GC-MIP检测性能的操作参数(包括等离子体观测位置,微波功率和He支持气流速)进行了最优化研究。结果表明,对C、H、D、O、S、P、F、Cl、Br和I元素来说,每个元素都有各自的一套最佳操作参数。此外,还对记忆效应进行了讨论。     

Biomimetic Donor–Acceptor Motifs in Conjugated Polymers for Promoting Exciton Splitting and Charge Separation

Natural photosynthesis serves as a model for energy and chemical conversions, and motivates the search of artificial systems that mimic nature′s energy‐ and electron‐transfer chains. However, bioinspired systems often suffer from the partial or even large loss of the charge separation state, and show moderate activity owing to the fundamentally different features of the multiple compounds. Herein, a selenium and cyanamide‐functionalized heptazine‐based melon (DA‐HM) is designed as a unique bioinspired donor–acceptor (D‐A) light harvester. The combination of the photosystem and electron shuttle in a single species, with both n‐ and p‐type conductivities, and extended spectral absorption, endows DA‐HM with a high efficiency in the transfer and separation of photoexcited charge carriers, resulting in photochemical activity. This work presents a unique conjugated polymeric system that shows great potential for solar‐to‐chemical conversion by artificial photosynthesis.     

Iridium‐Catalyzed Reductive Alkylations of Secondary Amides

Reported herein is the first direct, metal‐catalyzed reductive functionalization of secondary amides to give functionalized amines and heterocycles. The method is shown to have exceptionally broad scope with respect to suitable nucleophiles, which cover both hard and soft C nucleophiles as well as a P nucleophile. The reaction exhibits good chemoselectivity and tolerates several sensitive functional groups.     

Amino‐Assisted Anchoring of CsPbBr3 Perovskite Quantum Dots on Porous g‐C3N4 for Enhanced Photocatalytic CO2 Reduction

Halide perovskite quantum dots (QDs) have great potential in photocatalytic applications if their low charge transportation efficiency and chemical instability can be overcome. To circumvent these obstacles, we anchored CsPbBr₃ QDs (CPB) on NH_x‐rich porous g‐C₃N₄ nanosheets (PCN) to construct the composite photocatalysts via N?Br chemical bonding. The 20 CPB‐PCN (20 wt % of QDs) photocatalyst exhibits good stability and an outstanding yield of 149 μmol h^?1 g^?1 in acetonitrile/water for photocatalytic reduction of CO₂ to CO under visible light irradiation, which is around 15 times higher than that of CsPbBr₃ QDs. This study opens up new possibilities of using halide perovskite QDs for photocatalytic application.     

A Ligand System for the Flexible Functionalization of Quantum Dots via Click Chemistry

We present a novel ligand, 5‐norbornene‐2‐nonanoic acid, which can be directly added during established quantum dot (QD) syntheses in organic solvents to generate “clickable” QDs at a few hundred nmol scale. This ligand has a carboxyl group at one terminus to bind to the surface of QDs and a norbornene group at the opposite end that enables straightforward phase transfer of QDs into aqueous solutions via efficient norbornene/tetrazine click chemistry. Our ligand system removes the traditional ligand‐exchange step and can produce water‐soluble QDs with a high quantum yield and a small hydrodynamic diameter of approximately 12 nm at an order of magnitude higher scale than previous methods. We demonstrate the effectiveness of our approach by incubating azido‐functionalized CdSe/CdS QDs with 4T1 cancer cells that are metabolically labeled with a dibenzocyclooctyne‐bearing unnatural sugar. The QDs exhibit high targeting efficiency and minimal nonspecific binding.     

Synthesis via a direct adsorption method and characterization of Cu<Superscript>2+</Superscript>-doped CdTe quantum-dot-sensitized TiO<Subscript>2</Subscript> nanotubes for use as a photoanode

A direct adsorption method for the synthesis of Cu²⁺-doped CdTe quantum dot (QD)-sensitized TiO₂ nanotubes (TNTAs) for use as a photoanode is reported in this study. The influences of the molar concentration of Cu²⁺, the sensitization temperature, the sensitization time, and the loop index on the photovoltaic performance of the CdTe:Cu²⁺/TNTAswas investigated. Scanning electron microscopy images showed that the CdTe:Cu²⁺ QDs are well dispersed on the TNTA surface. UV–vis adsorption measurements showed that the visible absorption of the TNTAs was enhanced by the CdTe:Cu²⁺ QD sensitization. Whereas the power conversion efficiency (PCE) of the bare TNTAs was 0.11%, the maximum PCE of the CdTe:5%Cu²⁺/TNTAs was 3.70% with a sensitization time of 5.0 h, a sensitization temperature of 60 °C, and a loop index of 2. Therefore, CdTe:5%Cu²⁺/TNTAs may be employed in quantum-dot-sensitized solar cells.

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Graphical abstract The conversion efficiency of the CdTe: 5%Cu²⁺/TiO₂ nanotube arrays can reach a maximum of 3.7%, which is enhanced by 33-fold, on comparison with bare TiO₂ nanotube arrays (0.11%).

     

生物质炭的制备、改性以及在挥发性有机物吸附方面的应用

挥发性有机物（VOCs）是大气中重要的污染源之一,对环境和人类健康产生严重的危害。吸附法是工业中最常用的去除VOCs的方法,吸附剂是吸附技术的关键,生物质炭是一种由生物质基材料在高温下热解活化等工艺制得的炭材料,具有较高的比表面积、丰富的孔隙结构和化学活性表面,在环境污染控制领域具有广泛应用。基于最近的研究,本文系统地综述了常用于去除VOCs的生物质炭的制备和改性方法,以及生物质炭在吸附VOCs的应用研究。本文首要目标是评估生物质炭去除VOCs的能力,特别是经过各种改性和活化工艺后,评价生物质炭作为吸附剂去除VOCs的适用性;确定改性和活化后对VOCs吸附能力的影响;揭示生物质炭对VOCs可能存在的吸附机理。最后,文章也对生物质炭的再生提出了建议和展望。     

On a kinematic compatibility equation related to elastic stress-free joints and crystal twins

Consider the kinematic compatibility equation QFR = F(I + a n).Here Q and R are two 3×3 matrices representing two rotations, F is a 3×3 matrix with det (F) > 0, I is the 3×3 identity matrix, a and n are two vectors in the 3-dimensional Euclidean space R ³, and a n is the direct product. Assume F and R are given, and we solve for Q, a, n. We will first present a new proof of a criterion, due to Professor Jerry Ericksen, to be met by F and R for the existence of non-trivial solutions. Then we will give sufficient and necessary conditions for F and R under which the equation has solutions of special properties that are related to compound twins and multiple twins in crystals.