Triplet energy migration pathways from PbS quantum dots to surface-anchored polyacenes controlled by charge transfer

Nanoscale ◽  
2021 ◽  
Author(s):  
Guohui Zhao ◽  
Zongwei Chen ◽  
Kao Xiong ◽  
Guijie Liang ◽  
Jianbing Zhang ◽  
...  

Kinetic pathways of triplet energy transfer from photoexcited PbS QDs to surface-anchored tetracene and pentacene derivatives are dictated by charge-transfer energetics at the QD/molecule interface.

2019 ◽  
Author(s):  
Victor Gray ◽  
Jesse Allardice ◽  
Simon Dowland ◽  
Zhilong Zhang ◽  
James Xiao ◽  
...  

2019 ◽  
Author(s):  
Victor Gray ◽  
Jesse Allardice ◽  
Simon Dowland ◽  
Zhilong Zhang ◽  
James Xiao ◽  
...  

2020 ◽  
Vol 11 (17) ◽  
pp. 7239-7244
Author(s):  
Victor Gray ◽  
Zhilong Zhang ◽  
Simon Dowland ◽  
Jesse R. Allardice ◽  
Antonios M. Alvertis ◽  
...  

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Xiao Luo ◽  
Yaoyao Han ◽  
Zongwei Chen ◽  
Yulu Li ◽  
Guijie Liang ◽  
...  

AbstractThe mechanisms of triplet energy transfer across the inorganic nanocrystal/organic molecule interface remain poorly understood. Many seemingly contradictory results have been reported, mainly because of the complicated trap states characteristic of inorganic semiconductors and the ill-defined relative energetics between semiconductors and molecules used in these studies. Here we clarify the transfer mechanisms by performing combined transient absorption and photoluminescence measurements, both with sub-picosecond time resolution, on model systems comprising lead halide perovskite nanocrystals with very low surface trap densities as the triplet donor and polyacenes which either favour or prohibit charge transfer as the triplet acceptors. Hole transfer from nanocrystals to tetracene is energetically favoured, and hence triplet transfer proceeds via a charge separated state. In contrast, charge transfer to naphthalene is energetically unfavourable and spectroscopy shows direct triplet transfer from nanocrystals to naphthalene; nonetheless, this “direct” process could also be mediated by a high-energy, virtual charge-transfer state.


ACS Nano ◽  
2020 ◽  
Vol 14 (8) ◽  
pp. 10748-10749
Author(s):  
Victor Gray ◽  
Jesse R. Allardice ◽  
Zhilong Zhang ◽  
Simon Dowland ◽  
James Xiao ◽  
...  

2012 ◽  
Vol 109 (38) ◽  
pp. 15132-15135 ◽  
Author(s):  
Akitaka Ito ◽  
David J. Stewart ◽  
Zhen Fang ◽  
M. Kyle Brennaman ◽  
Thomas J. Meyer

Distance-dependent energy transfer occurs from the Metal-to-Ligand Charge Transfer (MLCT) excited state to an anthracene-acrylate derivative (Acr-An) incorporated into the polymer network of a semirigid poly(ethyleneglycol)dimethacrylate monolith. Following excitation, to Acr-An triplet energy transfer occurs followed by long-range, Acr-3An—Acr-An → Acr-An—Acr-3An, energy migration. With methyl viologen dication (MV2+) added as a trap, Acr-3An + MV2+ → Acr-An+ + MV+ electron transfer results in sensitized electron transfer quenching over a distance of approximately 90 Å.


2020 ◽  
Vol 142 (41) ◽  
pp. 17581-17588 ◽  
Author(s):  
Zhiyuan Huang ◽  
Zihao Xu ◽  
Tingting Huang ◽  
Victor Gray ◽  
Kasper Moth-Poulsen ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Runchen Lai ◽  
Yangyi Liu ◽  
Xiao Luo ◽  
Lan Chen ◽  
Yaoyao Han ◽  
...  

AbstractConventional wisdom posits that spin-triplet energy transfer (TET) is only operative over short distances because Dexter-type electronic coupling for TET rapidly decreases with increasing donor acceptor separation. While coherent mechanisms such as super-exchange can enhance the magnitude of electronic coupling, they are equally attenuated with distance. Here, we report endothermic charge-transfer-mediated TET as an alternative mechanism featuring shallow distance-dependence and experimentally demonstrated it using a linked nanocrystal-polyacene donor acceptor pair. Donor-acceptor electronic coupling is quantitatively controlled through wavefunction leakage out of the core/shell semiconductor nanocrystals, while the charge/energy transfer driving force is conserved. Attenuation of the TET rate as a function of shell thickness clearly follows the trend of hole probability density on nanocrystal surfaces rather than the product of electron and hole densities, consistent with endothermic hole-transfer-mediated TET. The shallow distance-dependence afforded by this mechanism enables efficient TET across distances well beyond the nominal range of Dexter or super-exchange paradigms.


ACS Nano ◽  
2020 ◽  
Vol 14 (4) ◽  
pp. 4224-4234 ◽  
Author(s):  
Victor Gray ◽  
Jesse R. Allardice ◽  
Zhilong Zhang ◽  
Simon Dowland ◽  
James Xiao ◽  
...  

2019 ◽  
Vol 10 (24) ◽  
pp. 6120-6124 ◽  
Author(s):  
Zihao Xu ◽  
Tao Jin ◽  
Yiming Huang ◽  
Karimulla Mulla ◽  
Francesco A. Evangelista ◽  
...  

Triplet energy transfer from quantum dots takes advantage of small energy loss during intersystem crossing.


Sign in / Sign up

Export Citation Format

Share Document