Department of Physics, University of Helsinki, Finland.
Science. 2013 Feb 22;339(6122):943-6. doi: 10.1126/science.1227385.
Atmospheric nucleation is the dominant source of aerosol particles in the global atmosphere and an important player in aerosol climatic effects. The key steps of this process occur in the sub-2-nanometer (nm) size range, in which direct size-segregated observations have not been possible until very recently. Here, we present detailed observations of atmospheric nanoparticles and clusters down to 1-nm mobility diameter. We identified three separate size regimes below 2-nm diameter that build up a physically, chemically, and dynamically consistent framework on atmospheric nucleation--more specifically, aerosol formation via neutral pathways. Our findings emphasize the important role of organic compounds in atmospheric aerosol formation, subsequent aerosol growth, radiative forcing and associated feedbacks between biogenic emissions, clouds, and climate.
大气成核是全球大气中气溶胶颗粒的主要来源,也是气溶胶气候效应的重要参与者。这个过程的关键步骤发生在亚 2 纳米(nm)的尺寸范围内,直到最近才有可能对其进行直接的尺寸分离观测。在这里,我们呈现了对大气纳米颗粒和簇的详细观测,直至 1nm 迁移直径。我们在 2nm 以下的直径范围内确定了三个不同的尺寸范围,为大气成核——更具体地说是通过中性途径形成气溶胶——构建了一个物理、化学和动态上一致的框架。我们的研究结果强调了有机化合物在大气气溶胶形成、随后的气溶胶生长、辐射强迫以及生物排放、云和气候之间的反馈中的重要作用。