Nanoflower Fe-base complex for efficient CO2 fixation under atmospheric pressure

被引:6
|
作者
Tu, Xuewei [1 ]
Sun, Qiang [2 ]
Zhu, Shouxin [1 ]
Sun, Can [1 ]
Hu, Yang [1 ]
Qu, Jingyi [1 ]
Zhu, Zhexiao [1 ]
Duan, Xiaofei [3 ,4 ]
Zhang, Xiang [5 ]
Zheng, Hui [1 ]
机构
[1] Hangzhou Normal Univ, Coll Mat Chem & Chem Engn, Hangzhou 310016, Peoples R China
[2] RMIT Univ, Australian Res Council, Sch Sci, Ctr Excellence Nanoscale BioPhoton CNBP, Melbourne, Vic 3001, Australia
[3] Univ Melbourne, Fac Sci, Melbourne TrACEES Platform, Parkville 3010, Australia
[4] Univ Melbourne, Fac Sci, Sch Chem, Parkville 3010, Australia
[5] Shaanxi Dexinxiang Energy Technol Co Ltd, Xian 710048, Shanxi, Peoples R China
来源
基金
澳大利亚研究理事会; 中国国家自然科学基金;
关键词
CO2; fixation; Cyclic carbonate; Photothermal catalysis; Nanoflower; PHOTOCATALYTIC REDUCTION; CO2; CONVERSION;
D O I
10.1016/j.jece.2024.112544
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The cycloaddition of CO 2 with epoxides to synthesize valuable chemicals is a promising strategy for advancing carbon neutrality. Herein, a novel iron -based complex (Fe@NTC) with a flower-like structure was employed as an efficient catalyst for the cycloaddition reaction between carbon dioxide and epoxides. Employed in the cycloaddition reaction between carbon dioxide and epoxides, Fe@NTC achieved remarkable conversion of cyclic carbonates, with efficiencies reaching up to 93% yield under UV irradiation. This exceptional performance is largely due to the catalyst 's abundant active sites and superior photothermal catalytic capabilities. Comprehensive characterization techniques revealed that its distinct flower -shaped morphology significantly boosted photocatalytic efficiency. Through meticulous optimization via an orthogonal experimental design, we established ideal reaction conditions, under which Fe@NTC demonstrated consistent stability in repeated cycles. This research not only highlighted the efficacy of Fe@NTC in CO 2 fixation but also paved the way for the development of innovative iron -based catalysts for environmental sustainability.
引用
收藏
页数:8
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