Pd-Decorated UiO-66-NH2@COF-Ph Heterojunction for Photothermal Catalytic CO2 Carbonylation Reaction to Quinazolinones
Source abstract
Abstract
Photothermal catalysis represents a promising approach for efficiently converting CO 2 into valuable fuels or chemical feedstocks. Nevertheless, the photothermal effect of traditional semiconductor-based photothermal catalysts is often insufficient to establish a relatively stable local temperature field primarily due to rapid heat dissipation, resulting from their limited visible-light responsiveness and poor charge separation efficiency. Herein, we present a core–shell porous heterostructure with a synergistic photothermal catalytic system for CO 2 fixation, which is constructed by intercalating Pd nanoparticles with a surface plasmon resonance (LSPR) effect into the UiO-66-NH 2 as the core and a triazine-based covalent-organic framework (COF) as the shell with high light absorption. Benefiting from the stable structure, favorable photosensitivity, uniformly distributed Pd catalytic centers, and inherent photothermal properties, the fabricated Pd@UiO-66-NH 2 @COF-Ph exhibits great catalytic performance and reusability for the carbonylation activity of CO 2 to quinazoline-2,4(1H,3H)-diones. This work provides a hopeful strategy for efficiently transforming CO 2 into meaningful chemicals under mild conditions and can also be readily adapted to other reaction processes.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Carbon dioxide utilization in catalysis · Asymmetric Hydrogenation and Catalysis · Covalent Organic Framework Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Magnetic Molecules and Magnetic Information Materials of Ministry of Education & School of Chemistry and Materials Science of Shanxi Normal University
College of Chemistry, Key Laboratory of Interface Science and Engineering in Advanced Material (MOE)
Taiyuan University of Technology
Funding
National Natural Science Foundation of China · Institute of Cultural Chemistry
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