Movilla José L, Planelles Josep, Climente Juan I
Departament d'Educació i Didàctiques Específiques, Universitat Jaume I, 12080 Castelló, Spain.
Departament de Química Física i Analítica, Universitat Jaume I, E-12080 Castelló de la Plana, Spain.
J Phys Chem Lett. 2020 May 7;11(9):3294-3300. doi: 10.1021/acs.jpclett.0c00855. Epub 2020 Apr 14.
We show theoretically that carriers confined in semiconductor colloidal nanoplatelets (NPLs) sense the presence of neighbor, cofacially stacked NPLs in their energy spectrum. When approaching identical NPLs, the otherwise degenerate energy levels red-shift and split, forming (for large stacks) minibands that are several millielectronvolts in width. Unlike in epitaxial structures, the molecular behavior does not result from quantum tunneling but from changes in the dielectric confinement. The associated excitonic absorption spectrum shows a rich structure of bright and dark states, whose optical activity and multiplicity can be understood from reflection symmetry and Coulomb tunneling. We predict spectroscopic signatures that should confirm the formation of molecular states, whose practical realization would pave the way for the development of nanocrystal chemistry based on NPLs.
我们从理论上表明,限制在半导体胶体纳米片(NPL)中的载流子在其能谱中能感知到相邻的、共面堆叠的NPL的存在。当接近相同的NPL时,原本简并的能级会发生红移和分裂,(对于大的堆叠)形成宽度为几毫电子伏特的微带。与外延结构不同,这种分子行为不是由量子隧穿引起的,而是由介电限制的变化导致的。相关的激子吸收光谱显示出丰富的亮态和暗态结构,其光学活性和多重性可以通过反射对称性和库仑隧穿来理解。我们预测了光谱特征,这些特征应能证实分子态的形成,其实际实现将为基于NPL的纳米晶体化学的发展铺平道路。