Type
ArticleAuthors
Zhang, Yuhai
Sinatra, Lutfan

Alarousu, Erkki
Yin, Jun

El-Zohry, Ahmed M.

Bakr, Osman

Mohammed, Omar F.

KAUST Department
Chemical Science ProgramFunctional Nanomaterials Lab (FuNL)
KAUST Catalysis Center (KCC)
KAUST Solar Center (KSC)
Material Science and Engineering Program
Physical Science and Engineering (PSE) Division
Ultrafast Laser Spectroscopy and Four-dimensional Electron Imaging Research Group
Date
2018-02-23Online Publication Date
2018-02-23Print Publication Date
2018-03-22Permanent link to this record
http://hdl.handle.net/10754/627632
Metadata
Show full item recordAbstract
Although ligands of long carbon chains are very crucial to form stable colloidal perovskite nanocrystals (NCs), they create a severe barrier for efficient charge injection or extraction in quantum-dot-based optoelectronics, such as light emitting diode or solar cell. Here, we report a new approach to preparing ligand-free perovskite NCs of CsPbBr, which retained high photoluminescence quantum yield (44%). Such an approach involves a polar solvent (acetonitrile) and two small molecules (ammonium acetate and cesium chloride), which replace the organic ligand and still protect the nanocrystals from dissolution. The successful removal of hydrophobic long ligands was evidenced by Fourier transform infrared spectroscopy, ζ potential analysis, and thermogravimetric analysis. Unlike conventional perovskite NCs that are extremely susceptible to polar solvents, the ligand-free CsPbBr NCs show robust resistance to polar solvents. Our ligand-free procedure opens many possibilities not only from a material hybridization perspective but also in optimizing charge injection and extraction in semiconductor quantum-dot-based optoelectronics applications.Citation
Zhang Y, Sinatra L, Alarousu E, Yin J, El-Zohry AM, et al. (2018) Ligand-Free Nanocrystals of Highly Emissive Cs4PbBr6 Perovskite. The Journal of Physical Chemistry C 122: 6493–6498. Available: http://dx.doi.org/10.1021/acs.jpcc.8b01735.Sponsors
This work was financially supported by King Abdullah University of Science and Technology (KAUST).Publisher
American Chemical Society (ACS)Additional Links
https://pubs.acs.org/doi/10.1021/acs.jpcc.8b01735ae974a485f413a2113503eed53cd6c53
10.1021/acs.jpcc.8b01735