Wilson Andrew J, Devasia Dinumol, Jain Prashant K
Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Chem Soc Rev. 2020 Jul 23. doi: 10.1039/d0cs00338g.
Single-molecule-level measurements are bringing about a revolution in our understanding of chemical and biochemical processes. Conventional measurements are performed on large ensembles of molecules. Such ensemble-averaged measurements mask molecular-level dynamics and static and dynamic fluctuations in reactivity, which are vital to a holistic understanding of chemical reactions. Watching reactions on the single-molecule level provides access to this otherwise hidden information. Sub-diffraction-limited spatial resolution fluorescence imaging methods, which have been successful in the field of biophysics, have been applied to study chemical processes on single-nanoparticle and single-molecule levels, bringing us new mechanistic insights into physiochemical processes. However, the scope of chemical processes that can be studied using fluorescence imaging is considerably limited; the chemical reaction has to be designed such that it involves fluorophores or fluorogenic probes. In this article, we review optical imaging modalities alternative to fluorescence imaging, which expand greatly the range of chemical processes that can be probed with nanoscale or even single-molecule resolution. First, we show that the luminosity, wavelength, and intermittency of solid-state photoluminescence (PL) can be used to probe chemical transformations on the single-nanoparticle-level. Next, we highlight case studies where localized surface plasmon resonance (LSPR) scattering is used for tracking solid-state, interfacial, and near-field-driven chemical reactions occurring in individual nanoscale locations. Third, we explore the utility of surface- and tip-enhanced Raman scattering to monitor individual bond-dissociation and bond-formation events occurring locally in chemical reactions on surfaces. Each example has yielded some new understanding about molecular mechanisms or location-to-location heterogeneity in chemical activity. The review finishes with new and complementary tools that are expected to further enhance the scope of knowledge attainable through nanometer-scale resolution chemical imaging.
单分子水平的测量正在给我们对化学和生物化学过程的理解带来一场革命。传统测量是在大量分子集合上进行的。这种集合平均测量掩盖了分子水平的动力学以及反应性方面的静态和动态波动,而这些对于全面理解化学反应至关重要。在单分子水平上观察反应能够获取这些原本隐藏的信息。亚衍射极限空间分辨率荧光成像方法在生物物理学领域取得了成功,已被应用于研究单纳米颗粒和单分子水平上的化学过程,为我们带来了关于物理化学过程的新机制见解。然而,使用荧光成像可研究的化学过程范围相当有限;化学反应必须设计成涉及荧光团或荧光探针。在本文中,我们综述了替代荧光成像的光学成像模式,这些模式极大地扩展了能够以纳米级甚至单分子分辨率探测的化学过程范围。首先,我们表明固态光致发光(PL)的发光度、波长和间歇性可用于探测单纳米颗粒水平上的化学转变。接下来,我们重点介绍一些案例研究,其中局部表面等离子体共振(LSPR)散射用于跟踪在单个纳米级位置发生的固态、界面和近场驱动的化学反应。第三,我们探讨表面增强拉曼散射和针尖增强拉曼散射在监测表面化学反应中局部发生的单个键解离和键形成事件方面的效用。每个例子都在分子机制或化学活性的位置间异质性方面产生了一些新的认识。综述最后介绍了新的补充工具,预计这些工具将进一步扩大通过纳米级分辨率化学成像可获得的知识范围。