Unraveling the stabilization mechanism of solid electrolyte interface on ZnSe by rGO in sodium ion battery

Transition metal selenides have been widely studied as anode materials of sodium ion batteries(SIBs),however,the investigation of solid-electrolyte-interface(SEI)on these materials,which is critical to the electrochemical performance of SIBs,remains at its infancy.Here in this paper,ZnSe@C nanoparticles were prepared from ZIF-8 and the SEI layers on these electrodes with and without reduced graphene oxide(rGO)layers were examined in details by X-ray photoelectron spectroscopies at varied charged/discharged states.It is observed that fast and complicated electrolyte decomposition reactions on ZnSe@C leads to quite thick SEI film and intercalation of solvated sodium ions through such thick SEI film results in slow ion diffusion kinetics and unstable electrode structure.However,the presence of rGO could efficiently suppress the decomposition of electrolyte,thus thin and stable SEI film was formed.ZnSe@C electrodes wrapped by rGO demonstrates enhanced interfacial charge transfer kinetics and high electrochemical performance,a capacity retention of 96.4%,after 1000 cycles at 5 A/g.This study might offer a simple avenue for the designing high performance anode materials through manipulation of SEI film.     

HPLC and HPCE analysis of microcystins RR, LR and YR present in cyanobacteria and water by using immunoaffinity extraction

Microcystins, which have their origin in species of cyanobacteria present in freshwaters, have recently been found to be important contaminants of the aquatic environment at trace levels. HPLC and HPCE with UV detection have been applied in the determination of such toxic compounds. Immunoaffinity chromatography for the selective extraction and clean-up of microcystins has been successfully applied to different matrices. Simple protocols for unambiguous determination of these toxins are presented and the immunoaffinity clean-up is compared with conventionally used solid phase extraction procedures. The development and optimisation of an on-line preconcentration procedure based on field amplified sample stacking for the analysis of microcystins by HPCE in the micellar electrokinetic chromatography mode is also described, using borate buffer with the anionic surfactant SDS, as separation electrolyte. Results indicate that sub-nanogram/gram content of microcystins can be detected in water samples, while sub-microgram/gram concentrations can be determined in algae samples.     

掺钕玻璃受激发射的脉冲光谱

众所周知,晶体和玻璃受激发射随时间变化的过程,一般是用强的脉冲光来表征。不外以前,用法布里-珀罗干涉仪和按时间扫描的电子转换管,看到了一个脉冲期间内,红宝石光激射器受激发射频率的变化,并比较了单个振荡峰值的频率。     

制备气相色谱在挥发性成分分离中的应用研究进展北大核心CSCD

分析型气相色谱仪对低沸点易挥发的有机化合物展现出优异的分离性能,通过在其色谱柱末端加装馏分收集装置,建立了现代制备气相色谱(Prep GC)技术,该技术可用于挥发性成分的快速分离富集。制备气相色谱仪是由分析型气相色谱仪改装而来,其进样系统、分离系统、检测系统、馏分收集系统也在不断地优化升级,以提高目标化合物的回收效率和纯度。Prep GC与现代波谱技术(如紫外可见吸收光谱、红外吸收光谱、拉曼光谱、质谱、X射线衍射、核磁共振波谱)耦合,可对分离富集得到的目标化合物的结构进行精准确证。近年来,与Prep GC在各种挥发性成分分离中的应用相关的报道逐渐增多,展现出良好的应用前景。然而,Prep GC在分离过程中也存在着无法制备热敏性化合物、分离成本高、易引入外源性污染等问题。该文根据近年来国内外研究学者的相关研究工作,对制备气相色谱仪的结构及其在精油单体化合物、昆虫信息素、食品和植物挥发性成分、地质生物标志物及持久性环境污染物的分离等领域的应用研究进展进行综述。最后,还对Prep GC在挥发性成分分离中的应用进行了总结与展望,旨在为拓展Prep GC应用领域提供参考。     

计算机科学技术在现代教育工作中的应用

美国、日本和欧美地区最早在教学的过程中使用计算机科学技术,但我国在八十年代才开始引用计算机教学。计算机科学技术在教学上的应用不仅可以减轻教师的压力,也可增加教学过程中知识的广泛性。计算机科学技术以其自身的优势不仅对我国现代教育产生巨大的影响,同时也渐渐成为现代教育中不可欠缺的一部分。     

Theoretical study of the oxidation of histidine by singlet oxygen

Herein we present a theoretical study of the reaction of singlet oxygen with histidine performed both in the gas phase and in aqueous solution. The potential energy surface of the reactive system was explored at the B3LYP/cc-pVTZ level of theory and the electronic energies were refined by means of single-point CCSD(T)/cc-pVTZ(-f) calculations. Solvent effects were taken into account by using a solvent continuum model (COSMO) and by adding explicit water molecules. The results show that the first step in the reaction mechanism corresponds to a nearly symmetric Diels-Alder addition of the singlet oxygen molecule to the imidazole ring to yield an endoperoxide, in agreement with experimental evidence. The intermediate formed can evolve along two different reaction paths leading to two isomeric hydroperoxides and, eventually, to open-chain or internally cyclised oxidised products. Water plays a significant role in stabilising the reaction structures by solvation and by acting as a bifunctional catalyst in the elimination/addition reaction steps. Our results explain why substituents at the N1-imidazole ring can hamper the evolution of the initial endoperoxide and result in Gibbs energy barriers in solution similar to those experimentally measured and suggest a likely route to the formation of peptide aggregates during the oxidation of histidine by singlet molecular oxygen.