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用于分子太阳能热能存储材料能量释放的碳基多相催化剂的合成与表征

Synthesis and Characterization of Carbon-Based Heterogeneous Catalysts for Energy Release of Molecular Solar Thermal Energy Storage Materials.

作者信息

Magson Lucien, Hölzel Helen, Aslam Adil S, Henninger Stefan, Munz Gunther, Moth-Poulsen Kasper, Knaebbeler-Buss Markus, Funes-Ardoiz Ignacio, Sampedro Diego

机构信息

Instituto de Investigación en Química de la Universidad de La Rioja (IQUR), C/Madre de Dios 53, Logroño 26004, La Rioja.

Department of Chemistry and Chemical Engineering, Chalmers University of Technology, Kemivagen 4, Gothenburg 412 96, Sweden.

出版信息

ACS Appl Mater Interfaces. 2024 Feb 14;16(6):7211-7218. doi: 10.1021/acsami.3c16855. Epub 2024 Feb 1.

Abstract

Molecular solar thermal energy storage (MOST) systems are rapidly becoming a feasible alternative to energy storage and net-zero carbon emission heating. MOST systems involve a single photoisomerization pair that incorporates light absorption, storage, and heat release processes in one recurring cycle. Despite significant recent advancements in the field, the catalytic back-reaction from MOST systems remains relatively unexplored. A wide range of applications is possible, contingent on the energy densities of the specific photoisomers. Here, we report platinum-, copper-, and nickel-based heterogeneous catalysts screened in batch conditions for the back-conversion reaction on the cyano-3-(4-methoxyphenyl)-norbornadiene/quadricyclane pair. Catalyst reactivities are investigated using structural characterization, imaging techniques, and spectroscopic analysis. Finally, the thermal stability is also explored for our best-performing catalysts.

摘要

分子太阳能热能存储(MOST)系统正迅速成为能量存储和净零碳排放供暖的可行替代方案。MOST系统涉及一个单一的光异构化对,该对在一个循环周期内整合了光吸收、存储和热释放过程。尽管该领域最近取得了重大进展,但MOST系统的催化逆反应仍相对未被探索。根据特定光异构体的能量密度,可能有广泛的应用。在此,我们报告了在间歇条件下筛选的用于氰基-3-(4-甲氧基苯基)-降冰片二烯/四环烷对逆转化反应的铂基、铜基和镍基多相催化剂。使用结构表征、成像技术和光谱分析来研究催化剂的反应活性。最后,还对我们性能最佳的催化剂的热稳定性进行了探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46d3/10875640/d1c13abbb0da/am3c16855_0001.jpg

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