IrAu 12 superatom modified by chiral diphosphines: doping-induced enhancement of chiroptical activity
Gold superatoms modified by chiral ligands are a new class of chiroptical nanomaterials, but improvement of their chiroptical properties, such as circular dichroism (CD) and circularly polarized luminescence (CPL), remains a challenge. In this work, we studied the effects of single-atom doping on th...
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Veröffentlicht in: | Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2023-02, Vol.11 (8), p.3095-3100 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Gold superatoms modified by chiral ligands are a new class of chiroptical nanomaterials, but improvement of their chiroptical properties, such as circular dichroism (CD) and circularly polarized luminescence (CPL), remains a challenge. In this work, we studied the effects of single-atom doping on the chiroptical properties of a representative Au
13
superatom using [Au
13
((
R
,
R
)-DIPAMP)
5
Cl
2
]
3+
and [Au
13
((
S
,
S
)-DIPAMP)
5
Cl
2
]
3+
(Au13-R/S; DIPAMP = 1,2-bis[(2-methoxyphenyl)phenylphosphino]ethane). We synthesized an enantiomeric pair of superatoms: [IrAu
12
((
R
,
R
)-DIPAMP)
5
Cl
2
]
+
and [IrAu
12
((
S
,
S
)-DIPAMP)
5
Cl
2
]
+
(IrAu12-R/S). Single-crystal X-ray diffraction analysis revealed that the icosahedral Ir@Au
12
core of IrAu12-R/S was more twisted along the Cl–Au–Ir–Au–Cl axis compared with the Au
13
core of Au13-R/S, leading to a larger absorption anisotropy factor. IrAu12-R/S exhibited a much higher photoluminescence quantum yield (∼70%) compared with Au13-R/S (15%) due to a larger energy gap between the highest occupied and the lowest unoccupied molecular orbitals. Although Ir doping did not appreciably enhance the photoluminescence anisotropy factors, the brightness of the CPL of IrAu12-R/S was five times higher than that of Au13-R/S. This work provides a rational guide for improving the chiroptical activity of Au superatoms
via
the doping-mediated manipulation of the geometric and electronic structures. |
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ISSN: | 2050-7526 2050-7534 |
DOI: | 10.1039/D2TC05321G |