Polymerized ionic liquid Co-catalysts driving photocatalytic CO2 transformation

被引:2
|
作者
Eisele, Lisa [1 ]
Hulaj, Blete [1 ]
Podsednik, Maximilian [2 ]
Laudani, Francesco [3 ]
Ayala, Pablo [4 ]
Cherevan, Alexey [4 ]
Foelske, Annette [3 ]
Limbeck, Andreas [5 ]
Eder, Dominik [4 ]
Bica-Schroder, Katharina [1 ]
机构
[1] TU Wien, Inst Appl & Synthet Chem, Getreidemark 9-163, A-1060 Vienna, Austria
[2] KAI Kompetenzzentrum Automobil & Industrieelektron, Argentinierstr 8, A-1040 Vienna, Austria
[3] TU Wien, Analyt Instrumentat Ctr, Lehargasse 6 Objekt 10, A-1060 Vienna, Austria
[4] TU Wien, Inst Mat Chem, Getreidemarkt 9-165, A-1060 Vienna, Austria
[5] TU Wien, Inst Chem Technol & Analyt, Getreidemarkt 9-164, A-1060 Vienna, Austria
来源
RSC SUSTAINABILITY | 2024年 / 2卷 / 09期
基金
奥地利科学基金会; 欧洲研究理事会;
关键词
CARBON-DIOXIDE; REDUCTION; CHEMISORPTION; CATALYSTS; OXYGEN;
D O I
10.1039/d4su00194j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photocatalytic production of CO from CO2 has the potential for safe and atom-economic production of feedstock chemicals via in situ carbonylation chemistry. We developed novel ionic liquid-based polymeric materials through radical copolymerisation of 1-butyl-3-vinylimidazolium chloride and photocatalytically active Re- and Ru-complexes that serve as the CO2 reduction catalyst and photosensitiser, respectively. The crosslinked polymeric framework allows for the facile immobilisation of molecular organometallic complexes for use as heterogenised catalysts; moreover, the involved imidazolium core units co-catalyze the reduction of CO2 via covalent interaction. The ratio of sensitiser and catalyst was analysed by laser ablation inductively coupled plasma mass spectroscopy (LA-ICP-MS) and set in relation to results from photocatalytic experiments. Ultimately, the heterogenous polymeric framework showed high selectivity for CO formation on photocatalytic CO2 reduction with improved stability to the corresponding homogenous system.
引用
收藏
页码:2524 / 2531
页数:8
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