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将二维黑磷催化的范围扩展到近红外光引发的自由基光聚合反应。

Expanding the Scope of 2D Black Phosphorus Catalysis to the Near-Infrared Light Initiated Free Radical Photopolymerization.

作者信息

Kocaarslan Azra, Eroglu Zafer, Yilmaz Gorkem, Metin Onder, Yagci Yusuf

机构信息

Department of Chemistry, Istanbul Technical University, Maslak, 34469 Istanbul, Turkey.

Department of Chemistry, Koç University, Sarıyer, 34450 Istanbul, Turkey.

出版信息

ACS Macro Lett. 2021 Jun 15;10(6):679-683. doi: 10.1021/acsmacrolett.1c00298. Epub 2021 May 13.

Abstract

In the drive toward the development of efficient and stable inorganic semiconductor materials with broadband solar absorption ability to induce various photochemical processes is a highly attractive research field. In this study, two-dimensional (2D) few-layer black phosphorus (BP) exfoliated in a solvent is utilized as photocatalyst to initiate the polymerization of various monomers under visible and near-IR (NIR) light irradiation. Upon the light exposure, few-layer BP generates excited electrons and holes, which undergo electron transfer reactions with the onium salts to form free radicals capable of initiating free radical polymerization. Among the onium salts tested, aryldiazonium salt was found to be the most efficient in the photopolymerization process owing to its favorable reduction potential with the conduction edge potential of BP. The presented strategy also provides the possibility for the in situ preparation of BP-polymer composite materials.

摘要

致力于开发具有宽带太阳能吸收能力以引发各种光化学过程的高效稳定无机半导体材料是一个极具吸引力的研究领域。在本研究中,在溶剂中剥离的二维(2D)少层黑磷(BP)被用作光催化剂,以在可见光和近红外(NIR)光照射下引发各种单体的聚合。光照后,少层BP产生激发电子和空穴,它们与鎓盐发生电子转移反应,形成能够引发自由基聚合的自由基。在所测试的鎓盐中,芳基重氮盐由于其与BP的导带边缘电位具有良好的还原电位,被发现在光聚合过程中效率最高。所提出的策略还为原位制备BP-聚合物复合材料提供了可能性。

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