采用原位聚合法制备了氯氧化铋(BiOCl)与聚苯胺(PANI)复合的Ⅱ型异质结光催化剂BiOCl/PANI，并采用X射线衍射(XRD)、傅里叶变换红外光谱(FTIR)、透射电子显微镜(TEM)、X射线光电子能谱(XPS)、紫外可见漫反射光谱(UV-Vis DRS)和N2吸附-脱附测试等多种技术手段对其进行了表征，考察了BiOCl/PANI在模拟可见光下对罗丹明B (RhB)的光催化降解性能。实验结果表明：BiOCl/PANI催化剂比PANI和BiOCl具有更高的光催化活性，在RhB质量浓度为50 mg·L^-1、PANI与BiOCl的物质的量之比为0.02∶1、50 mg·L^-1的催化剂条件下，所制备的BiOCl/PANI光催化150 min后，RhB降解率为98.8%，速率常数为0.031 min^-1；经过4次循环实验后，RhB降解率从98.8%降低至98.4%，表现出良好的稳定性和可重复利用性。光催化剂BiOCl/PANI实现了电子和空穴对的快速分离，降低了二者在催化剂内部的复合速率，提高了光催化性能。

仪器分析实验“分子荧光法测定罗丹明B的含量”存在实验过于简单、未考虑实际情况等问题。因此，本改进实验在三维荧光扫描模式下获取样本数据，不进行复杂预处理，而是运用化学计量学算法解析出目标分析物的纯信号，进而实现了染色辣椒中罗丹明6G和123的同时测定。本改进实验提高了学生全面考虑问题和创新解决问题的能力。

We used pentacarboxylic acid ligand 3, 5-di(2', 4'-dicarboxylphenyl) benzoic acid (H₅L) to synthesize two structural similarity lanthanide-cobalt heteronuclear bimetallic organic frameworks (Ln-Co-MOFs) by hydrothermal method: (C₂H₆NH₂)₅{[Eu₉Co(L)₆(H₂O)₅(OH)₄] ·5DMF}_n (1), (C₂H₆NH₂)₂{[Sm₉Co(L)₆(H₂O)₃Cl] ·5DMF}_n (2). The structures were characterized and the property was tested by single crystal X-ray diffraction, powder X-ray diffraction, thermogravimetry, infrared, fluorescence spectra, and magnetism. The results show that 1 and 2 both belong to the trigonal R3 space group and have novel 3D structures and good thermal stability. Among them, 1 has strong fluorescence properties, which can sensitively identify drug molecules sulfasalazine and organic molecules glutaraldehyde. The detection limits could reach 0.95 and 2.10 μmol·L^-1, respectively. In addition, 1 and 2 were antiferromagnetic at 1 kOe.

A simple two-step hydrothermal method synthesized four different CdS/Fe₃O₄ photocatalysts with varying ratios of mass of CdS to Fe₃O₄. The composition and morphology of the prepared samples were investigated using X-ray diffraction (XRD), Raman spectrum, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Solid UV reflectance spectra testing found that CdS/Fe₃O₄ nanocomposites had good light absorption throughout the spectral range, promoting their photocatalytic properties. Under visible light irradiation, CdS/Fe₃O₄ (2:5) with a mass ratio of 2:5 exhibited excellent photocatalytic performance, with a degradation rate of 98.8% for rhodamine B. Furthermore, after five cycles of photocatalytic degradation reaction, the rhodamine B degradation rate remained at 96.2%, indicating that the photocatalysts have good photocatalytic stability.

A flower-like BiOBr photocatalyst (CS/BiOBr) was prepared by using the carbon material derived from corn straw (CS) as the carrier. The prepared composites were characterized by X - ray diffraction (XRD), Fourier transform infrared (FIIR) spectra, scanning electron microscope (SEM), X - ray photoelectron spectra (XPS), and UV-Vis diffuse reflectance spectra (UV-Vis DRS). The SEM analyses indicate that the introduction of CS promotes the formation of a unique flower-like structure in BiOBr, which not only optimizes the efficiency of light capture but also increases the specific surface area of BiOBr. The bandgap of the composite was narrower compared with the pure BiOBr. The CS/BiOBr composites exhibited higher photocatalytic activity than pure CS and BiOBr under visible light irradiation, and a higher first-order reaction rate constant (k) of 0.043 7 min^-1 than BiOBr (0.014 6 min^-1), and exhibited excellent stability and reusability during the cyclic run. The enhanced photocatalytic activity is attributed to the efficient separation of photoinduced electrons and holes. Superoxide radicals and holes were the major active species.

高镍正极匹配锂金属负极是实现高比能锂电池的重要发展方向之一，然而，高比能锂电池体系存在体相结构稳定性差、与表界面难以兼容等共性问题，特别是在高截止电压、宽温域的实际工况条件下，表界面退化往往加速体相结构的破坏，造成电极材料性能快速衰退。相较于离子掺杂和表面包覆等改性手段，基于溶剂-锂盐优化或功能性添加剂主导的电解液诱导界面重构改性工程，可以同时实现对高比能正负极材料电化学循环改性，易于大规模工业生产应用。其中，功能性添加剂能极大提升电极/电解液界面兼容性，同时有利于调控电解液溶剂化结构，利用其电化学氧化/还原活性特征改变高比能电极/电解液电化学界面行为，从而实现高比能锂电池稳定循环。本文论述了不同功能性电解液添加剂在高镍正极和负极表面的成膜性、界面吸附稳定性、界面协同演变、酸水杂质清除等方面改性作用，为筛选和设计特定功能化添加剂实现高比能高镍锂全电池的稳定循环提供了新思路。