Ultrafast laser spectroscopy uncovers mechanisms of light energy conversion in photosynthesis and sustainable energy materials

IF 6.1 Q2 CHEMISTRY, PHYSICAL
D. Zigmantas, T. Polívka, P. Persson, V. Sundström
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引用次数: 6

Abstract

The invention of the laser in 1960 gave us the ruby laser, which generally produced chaotic pulses of light. Six years later, in 1966, a concept called passive mode-locking applied to neodymium-glass lasers produced reasonably well-behaving picosecond pulses. This triggered an intense activity, with respect to developing improved laser pulse sources, measurement techniques, and application to chemistry, physics, and biology. Initially, only ∼10 –ps-long pulses at a few wavelengths were available. Nevertheless, insight into the function of complex biological systems, like photosynthetic proteins, and molecules of chemical interest was gained in very early studies. Today, both duration and color of ultrashort pulses can be tuned to almost any value. This has of course opened up possibilities to study almost any atomic, molecular, or solid-state system and any dynamic process. This review focuses on the use of laser spectroscopy to investigate light energy conversion mechanisms in both natural photosynthesis and a topical selection of novel materials for solar energy conversion. More specifically, in photosynthesis we will review light harvesting and primary electron transfer; materials for solar energy conversion that we discuss include sensitized semiconductors (dye sensitized solar cells), polymer:fullerene and polymer:polymer bulk heterojunctions (organic solar cells), organometal halide perovskites, as well as molecular and hybrid systems for production of solar fuel and valuable chemicals. All these scientific areas, and in particular photosynthesis and the solar cell materials, have been extensively studied with ultrafast spectroscopy, resulting in a vast literature; a comprehensive review of the individual materials is, therefore, not feasible, and we will limit our discussion to work that we think has been of particular importance for understanding the function of the respective systems.
超快激光光谱揭示光合作用和可持续能源材料中的光能转换机制
1960年激光器的发明给了我们红宝石激光器,它通常会产生混乱的光脉冲。六年后的1966年,一种名为被动锁模的概念应用于钕玻璃激光器,产生了性能相当好的皮秒脉冲。这引发了一场激烈的活动,涉及开发改进的激光脉冲源、测量技术以及在化学、物理和生物学中的应用。最初,只有~10 –可以获得几个波长的ps长脉冲。然而,在早期的研究中,人们对复杂生物系统的功能有了深入的了解,如光合蛋白和化学感兴趣的分子。如今,超短脉冲的持续时间和颜色几乎可以调谐到任何值。这当然为研究几乎任何原子、分子或固态系统以及任何动态过程开辟了可能性。这篇综述的重点是使用激光光谱学来研究自然光合作用中的光能转换机制,以及太阳能转换新材料的局部选择。更具体地说,在光合作用中,我们将回顾光捕获和初级电子转移;我们讨论的太阳能转换材料包括敏化半导体(染料敏化太阳能电池)、聚合物:富勒烯和聚合物:聚合物本体异质结(有机太阳能电池),有机金属卤化物钙钛矿,以及用于生产太阳能燃料和有价化学品的分子和混合系统。所有这些科学领域,特别是光合作用和太阳能电池材料,都用超快光谱学进行了广泛的研究,产生了大量的文献;因此,对个别材料进行全面审查是不可行的,我们将把讨论局限于我们认为对理解各自系统的功能特别重要的工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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