相关实验视频
Updated: Jun 25, 2026

14:22
Activating Molecules, Ions, and Solid Particles with Acoustic Cavitation
Published on: April 11, 2014
金的素诱导的腐蚀
Enrico Doná1, Michael Cordin, Clemens Deisl
1Institute of Physical Chemistry, University of Innsbruck, Innrain 52a, A-6020 Innsbruck, Austria.
Journal of the American Chemical Society
|February 11, 2009
概括
与 (Pt) 表面的相互作用导致表面侵蚀和PtCl(4) 的形成. 退火修复缺陷,创建一个有序的附加层,类似于电解质沉积结果.
科学领域:
- 表面科学是一门学科.
- 材料化学 材料化学
- 物理化学 物理化学
背景情况:
- 了解吸附物-表面相互作用对于催化和材料科学至关重要.
- 表面广泛用于催化,使其与素的反应性成为一个关键的研究领域.
研究的目的:
- 在超高真空 (UHV) 条件下研究 (Cl) 与 (Pt) 表面的相互作用.
- 阐明在Pt上和压缩Cl时发生的结构和化学变化.
主要方法:
- 扫描道显微镜 (STM) 用于原子级表面成像.
- 低能电子衍射 (LEED) 用于表面结构分析.
- 温度编程脱吸 (TPD) 用于研究脱吸动力学.
- 密度函数理论 (DFT) 计算用于理论见解.
主要成果:
- 高达0.5个单层 (ML) 的Cl在Pt上形成稳定的吸附物结构.
- 将Cl压缩到更高的覆盖面会诱导Pt原子侵蚀,并形成PtCl(4) 五合体.
- 化修复Pt表面缺陷,形成一个长距离排序的PtCl(4)/Cl/Pt(110) 附加层.
- 与CO的共同吸收启动了没有挥发性产品的PtCl(4) 形成.
- (Br) 具有较低的腐蚀活性,使Pt表面保持完整.
结论:
- 显著改变了Pt(110) 的表面结构,导致缺陷形成和PtCl(4) 的物种.
- 在回火后观察到的附加层结构与电解质沉积形成的结构相似.
- 与的比较研究突出了表面的素的不同反应性.
更多相关视频
相关概念视频
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
Radical substitution reactions can be used to remove functional groups from molecules. The hydrogenolysis of alkyl halides is one such reaction, where the weak Sn–H bond in tributyltin hydride reacts with alkyl halides to form alkanes. Here, the reagent Bu3SnH yields tributyltin halide as a byproduct.
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
Electrophilic Addition to Alkynes: Hydrohalogenation
Electrophilic addition of hydrogen halides, HX (X = Cl, Br or I) to alkenes forms alkyl halides as per Markovnikov's rule, where the hydrogen gets added to the less substituted carbon of the double bond. Hydrohalogenation of alkynes takes place in a similar manner, with the first addition of HX forming a vinyl halide and the second giving a geminal dihalide.
Radical Substitution: Allylic Chlorination
Typically, when alkenes react with halogens at low temperatures, an addition reaction occurs. However, upon increasing the temperature or under reaction conditions that form radicals, providing a low but steady concentration of halogen radicals, allylic substitution reaction is favored. This is because allylic hydrogens are very reactive as the formed intermediate is resonance stabilized. For example, when propene is treated with chlorine in the gas phase at 400 °C, it undergoes allylic...
Halogens
Group 17 elements, known as halogens, are nonmetals. At room temperature, fluorine and chlorine are gases, bromine is a liquid, and iodine a solid. Astatine is a highly unstable radioactive element, so currently, most of its properties are unknown due to its short half-life. Tennessine is a synthetic element also predicted to be in this group.
Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene
Chlorination and bromination are important classes of electrophilic aromatic substitutions, where benzene reacts with chlorine or bromine in the presence of a Lewis acid catalyst to give halogenated substitution products. A Lewis acid such as aluminium chloride or ferric chloride catalyzes the chlorination, and ferric bromide catalyzes the bromination reactions. During the bromination of alkenes, bromine polarizes and becomes electrophilic. However, in the bromination of benzene, the bromine...
Halogenation of Alkenes
Halogenation is the addition of chlorine or bromine across the double bond in an alkene to yield a vicinal dihalide. The reaction occurs in the presence of inert and non-nucleophilic solvents, such as methylene chloride, chloroform, or carbon tetrachloride.
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.

