首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Formation of a Chemisorbed Water-Hydroxyl Phase on Cu(110) Mediated by Surface Transport.
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Formation of a Chemisorbed Water-Hydroxyl Phase on Cu(110) Mediated by Surface Transport.

机译:在表面迁移介导的Cu(110)上形成化学吸附的水羟基相。

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Under ambient conditions, most of the solid surfaces are commonly covered with water and oxygen both playing a crucial role in catalysis, corrosion, and electrochemistry. We present an STM study on water interaction with the oxygen preadsorbed Cu(110)-(2 X 1)-O surface. Under water adsorption at ~200 K, the (2 X 1) added-on Cu—O chains are gradually transformed into mobile copper-hydroxyls complexes. Long-range transport and condensation of the complexes induce nucleation and growth of 2D copper islands. Simultaneously the associated hydroxyls self- assemble with oncoming water molecules into a well-ordered 2D water-hydroxyl chemisorbed phase thermally stable up to a room temperature. We found that the assembly of the water-hydroxyl phase could be consistently described in terms of H bonds formation between the adsorbate species. We anticipate that the understanding of the forces driving the chemisorption will stimulate studies on water chemisorption on other metal surfaces, which are still far from being completed.
机译:在环境条件下,大多数固体表面通常都被水和氧气覆盖,两者在催化,腐蚀和电化学中都起着至关重要的作用。我们提出了与氧预吸附的Cu(110)-(2 X 1)-O表面的水相互作用的STM研究。在〜200 K的水吸附下,(2 X 1)附加的Cu-O链逐渐转化为可移动的铜-羟基络合物。配合物的长距离传输和凝聚诱导2D铜岛的形核和生长。同时,相关的羟基与即将到来的水分子自组装成在室温下热稳定的有序2D水-羟基化学吸附相。我们发现,可以根据吸附物之间的氢键形成一致地描述水-羟基相的组装。我们预计,对驱动化学吸附力的理解将刺激对其他金属表面上水化学吸附的研究,但这些研究仍远未完成。

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