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231226s2023 xx |||||o 00| ||eng c |
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|a 10.1002/adma.202207555
|2 doi
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|a pubmed25n1161.xml
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|a (DE-627)NLM348674953
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|a (NLM)36353881
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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| 100 |
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|a Wan, Xiaodong
|e verfasserin
|4 aut
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|a Ultralong Lifetime of Plasmon-Excited Electrons Realized in Nonepitaxial/Epitaxial AuCdS/CsPbBr3 Triple-Heteronanocrystals
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|c 2023
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 20.01.2023
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|a Date Revised 20.01.2023
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a © 2022 Wiley-VCH GmbH.
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|a Combination of the strong light-absorbing power of plasmonic metals with the superior charge carrier dynamics of halide perovskites is appealing for bio-inspired solar-energy conversion due to the potential to acquire long-lived plasmon-induced hot electrons. However, the direct coupling of these two materials, with Au/CsPbBr3 heteronanocrystals (HNCs) as a prototype, results in severe suppression of plasmon resonances. The present work shows that interfacial engineering is a key knob for overcoming this impediment, based on the creation of a CdS mediate layer between Au and CsPbBr3 forming atomically organized Au-CdS and CdS-CsPbBr3 interfaces by nonepitaxial/epitaxial combined strategy. Transient spectroscopy studies demonstrate that the resulting AuCdS/CsPbBr3 HNCs generate remarkably long-lived plasmon-induced charge carriers with lifetime up to nanosecond timescale, which is several orders of magnitude longer than those reported for colloidal plasmonic metal-semiconductor systems. Such long-lived carriers extracted from plasmonic antennas enable to drive CO2 photoreduction with efficiency outperforming previously reported CsPbBr3 -based photocatalysts. The findings disclose a new paradigm for achieving much elongated time windows to harness the substantial energy of transient plasmons through realization of synergistic coupling of plasmonic metals and halide perovskites
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|a Journal Article
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|a core-shell
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|a heteronanocrystal
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|a lattice mismatch
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|a perovskite
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|a plasmonic catalysis
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|a plasmonic nanostructures
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|a surface plasmon resonance
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|a Pan, Yue
|e verfasserin
|4 aut
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|a Xu, Yanjun
|e verfasserin
|4 aut
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1 |
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|a Liu, Jia
|e verfasserin
|4 aut
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|a Chen, Hailong
|e verfasserin
|4 aut
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1 |
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|a Pan, Rongrong
|e verfasserin
|4 aut
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1 |
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|a Zhao, Yizhou
|e verfasserin
|4 aut
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|a Su, Peiwu
|e verfasserin
|4 aut
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|a Li, Yuemei
|e verfasserin
|4 aut
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|a Zhang, Xiuming
|e verfasserin
|4 aut
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1 |
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|a Zhang, Shuping
|e verfasserin
|4 aut
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|a Li, Hongbo
|e verfasserin
|4 aut
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|a Su, Dong
|e verfasserin
|4 aut
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|a Weng, Yuxiang
|e verfasserin
|4 aut
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|a Zhang, Jiatao
|e verfasserin
|4 aut
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| 773 |
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|i Enthalten in
|t Advanced materials (Deerfield Beach, Fla.)
|d 1998
|g 35(2023), 3 vom: 10. Jan., Seite e2207555
|w (DE-627)NLM098206397
|x 1521-4095
|7 nnas
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| 773 |
1 |
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|g volume:35
|g year:2023
|g number:3
|g day:10
|g month:01
|g pages:e2207555
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| 856 |
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|u http://dx.doi.org/10.1002/adma.202207555
|3 Volltext
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|d 35
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