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The Evolution of Surface Chemistry. A Personal View of Building the Future on Past and Present Accomplishments

机译:表面化学的演变。在过去和现在的成就上构建未来的个人观点

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Surface chemistry, like other branches of physical chemistry, historically developed through macrosopic studies. These included measurements of adsorption-desorption equilibria (adsorption isotherms), spreading of monomolecular films, surface dissociation of diatomic molecules, and kinetic studies of desorption, sticking, and catalytic oxidation of CO and H_2. Models of surface structures were proposed by Langmuir and Taylor on the bases of experimental findings. Molecular level studies of surface chemistry were delayed as compared to other fields of physical chemistry until the late 1950s as instrumentation to detect properties of the very small number of surface atoms (10~(15) cm~(-2)) in the presence of a large number of bulk atoms (10~(22) cm~(-3)) were not available. At present we have over 65 techniques (photon, electron, molecule, and ion scattering, and scanning probes) that can investigate composition, atomic and electronic structures, and the dynamics of their motion with ≤1% of a monolayer sensitivity. Key results include: quantitative determinations of surface segregation of constituents that minimize surface free energy, discovery of clean surface reconstruction and adsorbate induced restructuring, and the uniquely high chemical activity of rough surfaces and defects (steps and kinks). In situ molecular studies during surface reaction reveal the need for restructuring of metal surface atoms by a highly mobile strongly adsorbed overlayer to maintain catalytic activity: additives that inhibit mobility on the surface poison chemical reactivity. New techniques permitting molecular surface studies at high pressures and at solid-liquid interfaces greatly accelerated the developments of molecular surface chemistry and permitted in situ studies of complex surface chemical phenomena: catalytic reactions, electrode surface chemistry, and polymer surfaces. As always, further developments of techniques control the rate of progress of molecular surface chemistry.
机译:与化学的其他分支一样,表面化学在历史上也是通过宏观研究发展起来的。这些包括吸附-解吸平衡(吸附等温线)的测量,单分子膜的扩散,双原子分子的表面离解以及对CO和H_2的解吸,粘附和催化氧化的动力学研究。 Langmuir和Taylor在实验结果的基础上提出了表面结构模型。与其他物理化学领域相比,表面化学的分子水平研究被推迟到1950年代后期,作为检测存在下极少量表面原子(10〜(15)cm〜(-2))的性能的仪器。大量的原子(10〜(22)cm〜(-3))不可用。目前,我们有65种以上的技术(光子,电子,分子和离子散射以及扫描探针)可以研究组成,原子和电子结构,以及它们的运动动力学,单层灵敏度≤1%。关键结果包括:定量测定使表面自由能最小化的成分的表面偏析,发现干净的表面重建结构和由吸附剂引起的重组,以及粗糙表面和缺陷(台阶和扭结)独特的高化学活性。表面反应过程中的原位分子研究表明,需要通过高度移动的强烈吸附的覆盖层来重组金属表面原子,以维持催化活性:抑制表面活性的添加剂会毒化化学反应性。允许在高压和固液界面进行分子表面研究的新技术极大地促进了分子表面化学的发展,并允许对复杂的表面化学现象进行原位研究:催化反应,电极表面化学和聚合物表面。与往常一样,技术的进一步发展控制着分子表面化学的发展速度。

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