X射线光电子能谱
材料科学
咔唑
溴化苄
电化学
纳米材料
光催化
共轭体系
化学工程
催化作用
聚合物
化学
有机化学
纳米技术
电极
物理化学
复合材料
工程类
作者
Bishal Boro,Priyanka Kalita,Aathilingam Vijayaprabhakaran,Duy Quang Dao,Subhajit Nandy,Keun Hwa Chae,Yogendra Nailwal,Murugavel Kathiresan,John Mondal
出处
期刊:ACS applied nano materials
[American Chemical Society]
日期:2023-06-22
卷期号:6 (13): 11788-11801
被引量:6
标识
DOI:10.1021/acsanm.3c01721
摘要
The electrochemical fixation of carbon dioxide (CO2) into organic halides is one of the most prominent strategies for mitigating atmospheric CO2 emission, along with the difficulties associated with the toxic and carcinogenic halogenated compounds. Cu-based nanomaterials have been explored for numerous applications in nanotechnology, including electrocatalysis, organic catalytic transformations, and photocatalysis. In this work, we have designed and developed a Cu-embedded carbazole-derived porous organic polymer (Cu@Cz-POP) nanohybrid by utilizing the Friedel–Crafts alkylation approach and employing 1,4-dimethoxybenzene as the cross-linking agent comprising unique characteristic features of the extended π-conjugated system along with an active metal center with tunable electrochemical properties. The Brunauer–Emmett–Teller surface area of the conjugated Cz-POP is found to be 1060 m2 g–1. The X-ray photoelectron spectroscopy (XPS) study demonstrates the formation of CuO nanoparticles in the polymeric framework. X-ray absorption fine structure analysis (EXAFS) also reveals the existence of CuO with a smaller fraction of Cu in the polymeric framework, which is corroborated with the XPS analysis. The Cu@Cz-POP nanohybrid is fabricated by drop-casting over a Ni foam, showing promising electrocatalytic activity toward electrocarboxylation of benzyl bromide in 0.1 M TBA·BF4/CH3CN with saturated CO2 medium with a current density of 120 mA cm–2 delivering 65% yield of phenylacetic acid (PAA) as the primary product along with traces of benzyl 2-phenylacetate (BPA) and 1,2-diphenylethane (DPE), and the turnover frequency is found to be 8.556 × 10–7 s–1. Density functional theory calculations demonstrate that CuO is adsorbed more favorably at the N1 nitrogen atom of Cz-POP. An electron transfer from the N1 atom and the aromatic rings of Cz-POP to the CuO center is observed and confirmed by the overlap of alpha orbitals.
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