Recent advancements in the molecular design of deep-red to near-infrared light-absorbing photocatalysts

被引:4
作者
Zhong, Minling [1 ]
Sun, Yujie [1 ]
机构
[1] Univ Cincinnati, Dept Chem, Cincinnati, OH 45221 USA
来源
CHEM CATALYSIS | 2024年 / 4卷 / 08期
基金
美国国家科学基金会;
关键词
TRANSITION-METAL-COMPLEXES; PHOTOREDOX CATALYSIS; 2-PHOTON ABSORPTION; PYRROLIDINE DERIVATIVES; UP-CONVERSION; C-C; EXCITATION; OXIDATION; NANOPARTICLES; SPECTROSCOPY;
D O I
10.1016/j.checat.2024.100973
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photocatalysis has traditionally relied on photocatalysts that primarily absorb short-wavelength ultraviolet-visible (UV-vis) light. However, recent advancements have led to the development of photocatalysts that can absorb deep-red to near-infrared light. These near-infrared photocatalysts (NIR-PCs) offer distinct advantages over traditional UV-vis photocatalysts, including deeper tissue penetration and reduced interference from competing absorption processes. Herein, we summarize the latest advancements in their molecular design based on three activation mechanisms: one-photon absorption, triplet-triplet annihilation upconversion, and two-photon absorption. This review aims to present not only various organic transformations facilitated by NIR-PCs but also the diverse molecular engineering strategies that have been employed in the design and development of NIR-PCs, particularly focusing on those with exceptional absorption capabilities in the NIR region. Finally, a brief overview of the current challenges and opportunities for future explorations of NIR photocatalysis is presented, underscoring the growing significance of NIR-PCs in advancing the frontiers of photocatalysis.
引用
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页数:19
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