On the absence of a phonon bottleneck in strongly confined CsPbBr3 perovskite nanocrystals (Dedicated to Dalian Institute of Chemical Physics, CAS, on the occasion of its 70th anniversary.)

• Published in: Chemical science (Cambridge) 2019, Vol.10 (23), p.5983-5989
• Main Authors: Li, Yulu, Lai, Runchen, Luo, Xiao, Liu, Xue, Ding, Tao, Lu, Xin, Wu, Kaifeng
• Format: Article
• Language: English
• Subjects: Energy dissipation; Energy gap; Excitons; Lead compounds; Metal halides; Nanocrystals; Organic chemistry; Perovskites; Phonons; Photovoltaic cells; Quantum confinement; Quantum dots; Solar cells
• ISSN: 2041-6520; 2041-6539
• DOI: 10.1039/c9sc01339c

In traditional solar cells, photogenerated energetic carriers (so-called hot carriers) rapidly relax to band edges via emission of phonons, prohibiting the extraction of their excess energy above the band gap. Quantum confined semiconductor nanocrystals, or quantum dots (QDs), were predicted to have long-lived hot carriers enabled by a phonon bottleneck, i.e., the large inter-level spacings in QDs should result in inefficient phonon emissions. Here we study the effect of quantum confinement on hot carrier/exciton lifetime in lead halide perovskite nanocrystals. We synthesized a series of strongly confined CsPbBr3 nanocrystals with edge lengths down to 2.6 nm, the smallest reported to date, and studied their hot exciton relaxation using ultrafast spectroscopy. We observed sub-ps hot exciton lifetimes in all the samples with edge lengths within 2.6–6.2 nm and thus the absence of a phonon bottleneck. Their well-resolved excitonic peaks allowed us to quantify hot carrier/exciton energy loss rates which increased with decreasing NC sizes. This behavior can be well reproduced by a nonadiabatic transition mechanism between excitonic states induced by coupling to surface ligands.