配体(生物化学)
量子点
吸收(声学)
悬空债券
胶体
光化学
轨道能级差
吸光度
材料科学
钝化
化学
结晶学
纳米技术
物理化学
分子
光电子学
图层(电子)
有机化学
生物化学
色谱法
复合材料
受体
硅
作者
Daniel M. Kroupa,Márton Vörös,Nicholas P. Brawand,Noah D. Bronstein,Brett W. McNichols,Chloe Castañeda,Arthur J. Nozik,Alan Sellinger,Giulia Galli,Matthew C. Beard
标识
DOI:10.1021/acs.jpclett.8b01451
摘要
We studied the optical absorption enhancement in colloidal suspensions of PbS quantum dots (QD) upon ligand exchange from oleate to a series of cinnamate ligands. By combining experiments and ab initio simulations, we elucidate physical parameters that govern the optical absorption enhancement. We find that, within the cinnamate/PbS QD system, the optical absorption enhancement scales linearly with the electronic gap of the ligand, indicating that the ligand/QD coupling occurs equally efficient between the QD and ligand HOMO and their respective LUMO levels. Disruption of the conjugation that connects the aromatic ring and its substituents to the QD core causes a reduction of the electronic coupling. Our results further support the notion that the ligand/QD complex should be considered as a distinct chemical system with emergent behavior rather than a QD core with ligands whose sole purpose is to passivate surface dangling bonds and prevent agglomeration.
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