Ruthenium Dye Excitations and Relaxations in Natural Sunlight
Author:
Affiliation:
1. Chemical Sciences Division, Lawrence Berkeley National Laboratory Berkeley, California 94720, United States
Funder
U.S. Department of Energy
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jpca.1c02386
Reference27 articles.
1. Vibrational Relaxation and Redistribution Dynamics in Ruthenium(II) Polypyridyl-Based Charge-Transfer Excited States: A Combined Ultrafast Electronic and Infrared Absorption Study
2. Broadband Femtosecond Fluorescence Spectroscopy of [Ru(bpy)3]2+
3. Direct observation of the ultrafast intersystem crossing in tris(2,2′-bipyridine)ruthenium(II) using femtosecond stimulated Raman spectroscopy
4. Ultrafast Relaxations in Ruthenium Polypyridyl Chromophores Determined by Stochastic Kinetics Simulations
5. [Ru(bpy)3]2+∗ revisited. Is it localized or delocalized? How does it decay?
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. The Role of Spin–Orbit Coupling in the Linear Absorption Spectrum and Intersystem Crossing Rate Coefficients of Ruthenium Polypyridyl Dyes;The Journal of Physical Chemistry A;2024-09-04
2. Correction to “Ruthenium Dye Excitations and Relaxations in Natural Sunlight”;The Journal of Physical Chemistry A;2023-02-27
3. Water oxidation by a dye-catalyst diad in natural sunlight: timing and coordination of excitations and reactions across timescales of picoseconds to hours;Chemical Science;2023
4. A quantitative model of charge injection by ruthenium chromophores connecting femtosecond to continuous irradiance conditions;The Journal of Chemical Physics;2022-12-28
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