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不同连接阴离子的表面生长配位聚合物的电子诱导化学。

Electron-induced chemistry of surface-grown coordination polymers with different linker anions.

机构信息

University of Bremen, Faculty 2 (Chemistry/Biology), Institute for Applied and Physical Chemistry, Leobener Straße 5, Postfach 330440, D-28334 Bremen, Germany.

出版信息

Phys Chem Chem Phys. 2019 Jan 30;21(5):2351-2364. doi: 10.1039/c8cp07028h.

Abstract

Electron beam processing of surface-grown coordination polymers is a versatile approach to the fabrication of nanoscale surface structures. Depending on their molecular components, these materials can be converted into pure metallic particles or they can be activated to become a template for the spatially selective decomposition of suitable gaseous precursor molecules and subsequent autocatalytic growth of deposits. However, insight into the fundamental electron-induced chemistry for such processes has been scarce so far. Therefore, we investigated the electron-induced reactions of three self-assembled copper-containing materials, namely, copper(ii) oxalate, copper(ii) squarate, and copper(ii) 1,3,5-benzenetricarboxylate (HKUST-1) which were grown on the surface of self-assembled monolayers of mercaptoundecanoic acid in a layer-by-layer approach from copper(ii) acetate and various linker molecules. Changes incurred to these materials during electron irradiation were monitored by four complementary techniques. Reflection absorption infrared spectroscopy (RAIRS) and X-ray photoelectron spectroscopy (XPS) were used to identify the chemical species that are formed upon electron exposure. The temporal evolution of electron-stimulated desorption (ESD) of neutral volatile fragments was monitored to reveal the kinetics governing the decomposition of the different materials. Furthermore, the morphology was investigated by helium ion microscopy (HIM). A detailed analysis of the results for the different linker molecules provides new insights into the electron-induced chemistry of such surface-grown layers.

摘要

电子束处理表面生长的配位聚合物是一种制造纳米尺度表面结构的通用方法。根据其分子成分,这些材料可以转化为纯金属颗粒,也可以被激活成为空间选择性分解合适的气态前体分子并随后进行自催化沉积的模板。然而,迄今为止,对于这些过程的基本电子诱导化学还缺乏深入了解。因此,我们研究了三种自组装含铜材料(即草酸铜(ii)、均苯三甲酸铜(ii)和 1,3,5-苯三甲酸铜(ii)(HKUST-1))在电子辐照下的反应,这些材料是通过层层自组装的方法从醋酸铜(ii)和各种连接分子在巯基十一酸自组装单层表面上生长的。通过四种互补技术监测这些材料在电子辐照下的变化。反射吸收红外光谱(RAIRS)和 X 射线光电子能谱(XPS)用于鉴定电子暴露后形成的化学物质。监测中性挥发性碎片的电子刺激解吸(ESD)的时间演化,以揭示不同材料分解的动力学。此外,通过氦离子显微镜(HIM)研究了形貌。对不同连接分子的结果进行详细分析,为这种表面生长层的电子诱导化学提供了新的见解。

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