Goldzak Tamar, McIsaac Alexandra R, Van Voorhis Troy
Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA, USA.
Department of Chemistry, Columbia University, New York, NY, USA.
Nat Commun. 2021 Feb 9;12(1):890. doi: 10.1038/s41467-021-21153-z.
Colloidal CdSe nanocrystals (NCs) have shown promise in applications ranging from LED displays to medical imaging. Their unique photophysics depend sensitively on the presence or absence of surface defects. Using simulations, we show that CdSe NCs are inherently defective; even for stoichiometric NCs with perfect ligand passivation and no vacancies or defects, we still observe that the low energy spectrum is dominated by dark, surface-associated excitations, which are more numerous in larger NCs. Surface structure analysis shows that the majority of these states involve holes that are localized on two-coordinate Se atoms. As chalcogenide atoms are not passivated by any Lewis base ligand, varying the ligand should not dramatically change the number of dark states, which we confirm by simulating three passivation schemes. Our results have significant implications for understanding CdSe NC photophysics, and suggest that photochemistry and short-range photoinduced charge transfer should be much more facile than previously anticipated.
胶体硒化镉纳米晶体(NCs)在从发光二极管显示器到医学成像等一系列应用中展现出了前景。它们独特的光物理性质敏感地取决于表面缺陷的存在与否。通过模拟,我们表明硒化镉纳米晶体本质上是有缺陷的;即使对于具有完美配体钝化且没有空位或缺陷的化学计量比纳米晶体,我们仍然观察到低能谱由与表面相关的暗激发主导,在较大的纳米晶体中这种激发更多。表面结构分析表明,这些态中的大多数涉及局域在双配位硒原子上的空穴。由于硫族原子不会被任何路易斯碱配体钝化,改变配体不应显著改变暗态的数量,我们通过模拟三种钝化方案证实了这一点。我们的结果对于理解硒化镉纳米晶体的光物理性质具有重要意义,并表明光化学和短程光致电荷转移应该比以前预期的要容易得多。