石墨炉原子吸收法测定食品中镍的研究

建立了测定食品中镍的石墨炉原子吸收法，方法的最低检出限为１．６０μｇ／Ｌ，标准参考物牡蛎镍的测定值怀保证值偏差小于５％，回收率在８６．０％￣１０３．０％之间，并对我国八大类食品中镍含量本底值作了调查。     

空气—乙炔火焰中铝对铂的干扰规律,干扰机理及其应用研究

在不同介质中，少量铝对铂的吸光度均有抑制作用，随着铝的浓度增加，则表现为增感作用，其中在硝酸和硫酸介质５０００μｇ／ｍｌ的铝可使铂的吸光度分别增加９０％和１７８％，铝对铂的干扰可分为与浓度有关及与浓度无关的化学干扰，在硝酸介质中５０００μｇ／ｍｌ的铝对０－５０μｇ／ｍｌ铂的干扰与浓度无关，在该条件下可使用标准加入法。在硝酸介质中，５０００μｇ／ｍｌ的铝还可用作２５μｇ／ｍｌ钠对２５μｇ／ｍｌ铂干扰     

<新概念物理教程·热学>改革的思路

结合《新概念物理教程．热学》的编写，阐述了热学教学改革的主要思路。     

巯基棉富集─火焰原子吸收分光光度法测定水中的微量铁

本文详细考查了巯基棉富集Ｆｅ（Ⅲ）的条件，发现微量铁（Ⅲ）在ｐＨ值为５－８的条件下能为巯基棉定量吸附．１ｍｏｌ／Ｌ盐酸５ｍＬ能将巯基棉吸附的Ｆｅ（Ⅲ）定量洗脱，０．１ｇ巯基棉的饱和吸附量为９０μｇ，样品分析测定结果的相对标准偏差小于３．４％，９８．４％－９８．８％。     

双硫腙-活性炭柱富集分离水中痕量铅的条件研究

本文研究了用活性炭加双硫腙柱富集、分离水中痕量铅的适宜条件。用火焰原子吸收法分析了不同分离条件下铅的回收率。并讨论了几种干扰离子的影响情况。     

TEM01模式激光对两能级原子的作用力研究

推导了两能级原子在稳态和小速度一阶微扰近似下的受力矢量方程，并分析表明ＴＥＭ０１模光场以原子的作用力中存在旋涡力，对在大正失谐δ〉〉Ω０〉〉Г和ｚ〈〈ｚ０＝ｋｗ＾２／λ条件下的ＴＥＭ０１模行波和驻波场中原子的受力进行了分析，对行波场，自发辐射对原子运动的影响很大，但在ｒ〈〈λ区域内原子受到横向囚禁力；对驻波场，自发辐射的影响可以忽略，考虑在ｚ方向波长范围内原子的平均受力得到的结论为：在横向，除了有     

高熵纳米合金在电化学催化中的应用

The implementation of clean energy techniques, including clean hydrogen generation, use of solar-driven photovoltaic hybrid systems, photochemical heat generation as well as thermoelectric conversion, is crucial for the sustainable development of our society. Among these promising techniques, electrocatalysis has received significant attention for its ability to facilitate clean energy conversion because it promotes a higher rate of reaction and efficiency for the associated chemical transformations. Noble-metal-based electrocatalysts typically show high activity for electrochemical conversion processes. However, their scarcity and high cost limit their applications in electrocatalytic devices. To overcome this limitation, binary catalysts prepared by alloying with transition metals can be used. However, optimization of the activity of the binary catalysts is considerably limited because of the presence of the miscibility gap in the phase diagram of binary alloys. The activity of binary electrocatalysts can be attributed to the adsorption energy of molecules and intermediates on the surface. High-entropy alloys (HEAs), which consist of diverse elements in a single NP, typically exhibit better physical and/or chemical properties than their single-element counterparts, because of their tunable composition and inherent surface complexity. Further, HEAs can improve the performance of binary electrocatalysts because they exhibit a near-continuous distribution of adsorption energy. Recently, HEAs have gained considerable attention for their application in electrocatalytic reactions. This review summarizes recent research advances in HEA nanostructures and their application in the field of electrocatalysis. First, we introduce the concept, structure, and four core effects of HEAs. We believe that this part will provide the basic information about HEAs. Next, we discuss the reported top-down and bottom-up synthesis strategies, emphasizing on the carbothermal shock method, nanodroplet-mediated electrodeposition, fast moving bed pyrolysis, polyol process, and dealloying. Other methods such as combinatorial co-sputtering, ultrashort-pulsed laser ablation, ultrasonication-assisted wet chemistry, and scanning-probe block copolymer lithography are also highlighted. Among these methods, wet chemistry has been reported to be effective for the formation of nano-scale HEAs because it facilitates the concurrent reduction of all metal precursors to form solid-solution alloys. Next, we present the theoretical investigation of HEA nanocatalysts, including their thermodynamics, kinetic stability, and adsorption energy tuning for optimizing their catalytic activity and selectivity. To elucidate the structure–property relationship in HEAs, we summarize the research progress related to electrocatalytic reactions promoted by HEA nanocatalysts, including the oxygen reduction reaction, oxygen evolution reaction, hydrogen evolution reaction, methanol oxidation reaction, and CO₂ reduction reaction. Finally, we discuss the challenges and various strategies toward the development of HEAs.