Polaronic-Distortion-Driven Enhancement of Excitonic Auger Recombination in ZnO Nanoparticles

TL;DR

This study uncovers how polaronic distortions driven by Auger recombination influence the optoelectronic behavior of ZnO nanoparticles, revealing structural dynamics that affect luminescence and nonradiative processes.

Contribution

It provides new insights into the structural origin of Auger recombination in ZnO nanoparticles using advanced spectroscopy and diffraction techniques.

Findings

Hot holes are captured by oxygen vacancies causing local distortions.

Recombination of trapped holes accelerates lattice thermalization.

Formation of exciton-polaron complexes explains long-lived luminescence.

Abstract

The surface effect and quantum confinement render nanomaterials the optoelectronic properties more susceptible to nonradiative processes than their bulk counterparts. These nonradiative processes usually contain a series of interwoven and competing sub-processes, which are challenging to disentangle. Here, we investigate the structural origin of Auger recombination in ZnO nanoparticles using transient absorption spectroscopy and ultrafast electron diffraction. The photogenerated hot holes are captured by oxygen vacancies through an Auger mechanism, inducing significant local structural distortions around the oxygen vacancy and its neighboring zinc tetrahedron on a sub-picosecond timescale. The recombination of trapped holes accelerates the lattice thermalization and stabilizes the formed small hole polarons. Subsequently, the recombination of localized polarons forms a confined exciton-polaron complex that may account for the long-lived (>7 ns) visible luminescence observed in ZnO nanoparticles. Our findings are potentially applicable to other transition metal oxide nanomaterials, bringing insights for the optimization of their functional properties.