催化作用
咔唑
紧身衣
电化学
二氧化碳电化学还原
二氧化碳
还原(数学)
金属
光化学
材料科学
化学
无机化学
有机化学
电极
一氧化碳
荧光
光学
物理化学
数学
物理
几何学
作者
Mücahit Özdemir,Sude Uluçay,Sinem Altınışık,Baybars Köksoy,Bahattin Yalçın,Sermet Koyuncu
标识
DOI:10.1002/adsu.202400812
摘要
Abstract In this study, a cross‐linked boron dipyrromethene (BODIPY) photocatalyst containing a carbazole donor group designed for photoelectrocatalytic carbon dioxide (CO 2 ) reduction is synthesized and characterized. The BODIPY‐based system, coated onto a platinum surface, is evaluated for its electrochemical and photocatalytic performance under light illumination. Cyclic voltammetry (CV) and chronoamperometry measurements reveals enhanced photocurrent responses, confirming the catalyst's ability to effectively drive CO 2 reduction. Gas chromatography/mass spectrometry (GC‐MS) analysis identifies the formation of ethanol (C 2 H 5 OH) as a major reaction product, showing that its yield increased with extended reaction times. Additionally, the photocatalyst demonstrates remarkable performance with significantly increasing turnover numbers (TON) and turnover frequencies (TOF) over time, indicating stable and sustained catalytic activity. With a Faradaic efficiency of 34.79% at a potential of ‐1.15 V, this BODIPY system exhibits both high activity and long‐term stability. The combination of efficient electron transfer and visible light absorption by the carbazole‐BODIPY donor‐acceptor structure positions this system as a highly promising candidate for sustainable CO 2 conversion applications.
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