电合成
循环伏安法
材料科学
结晶度
化学工程
X射线光电子能谱
薄膜
无定形固体
电化学
纳米技术
化学
有机化学
物理化学
复合材料
电极
工程类
作者
Sara Realista,Ana Rosanete Reis,Duarte Borralho,V. Corregidor,L.C. Alves,Sarah Juliane Oliveira Magalhães,Telmo Nunes,Ana S. Viana,João Pires,Ana Maria Ferraria,Ana M. Botelho do Rego,Paulo N. Martinho
标识
DOI:10.1021/acs.jpcc.4c02651
摘要
High Resolution Image Download MS PowerPoint Slide This study examines the electrosynthesis of novel iron-organic films via cathodic electrodeposition using cyclic voltammetry to establish suitable deposition potentials for two different organic linkers: 2,5-dihydroxyterephthalic acid (DOBDC) and 3,3′-dihydroxybiphenyl-4,4′-dicarboxylic acid (BPP). The synthesis process focuses on the coordination of carboxylate to iron centers, producing amorphous films. Analytical techniques including infrared spectroscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, atomic force microscopy (AFM), and a combination of particle-induced X-ray emission and Rutherford backscattering spectrometry were employed to characterize the films’ chemical, morphological, and structural properties. AFM analysis highlighted the evolution of film morphology with deposition time, revealing a transition from highly ordered to more random structures, influencing film crystallinity. Electrochemical assessments demonstrated the stability and electroactive nature of the films, with their behavior dependent on the specific linker used, reflected in the varied electrochemical responses and film properties observed. The study not only refines the synthesis process for metal–organic films but also delineates the impact of synthesis parameters such as linker type, deposition time, and applied potential on the properties of the resulting materials, paving the way for future investigations into diverse electrosynthesis conditions and deprotonation mechanisms for creating innovative metal–organic materials.
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