All-inorganic perovskite nanocrystal assisted extraction of hot electrons and biexcitons from photoexcited CdTe quantum dots. Issue 2 (13th December 2017)
- Record Type:
- Journal Article
- Title:
- All-inorganic perovskite nanocrystal assisted extraction of hot electrons and biexcitons from photoexcited CdTe quantum dots. Issue 2 (13th December 2017)
- Main Title:
- All-inorganic perovskite nanocrystal assisted extraction of hot electrons and biexcitons from photoexcited CdTe quantum dots
- Authors:
- Mondal, Navendu
De, Apurba
Samanta, Anunay - Abstract:
- Abstract : Harvesting of hot electrons and biexcitons from CdTe quantum dots by all-inorganic perovskite nanocrystals is demonstrated through femtosecond transient absorption measurements. Abstract : Excitation of semiconductor quantum dots (QDs) by photons possessing energy higher than the band-gap creates a hot electron–hole pair, which releases its excess energy as waste heat or under certain conditions (when hν > 2 E g ) produces multiple excitons. Extraction of these hot carriers and multiple excitons is one of the key strategies for enhancing the efficiency of QD-based photovoltaic devices. However, this is a difficult task as competing carrier cooling and relaxation of multiple excitons (through Auger recombination) are ultrafast processes. Herein, we study the potential of all-inorganic perovskite nanocrystals (NCs) of CsPbX3 (X = Cl, Br) as harvesters of these short-lived species from photo-excited CdTe QDs. The femtosecond transient absorption measurements show CsPbX3 mediated extraction of both hot and thermalized electrons of the QDs (under a low pump power) and (under a high pump fluence) extraction of multiple excitons prior to their Auger assisted recombination. A faster timescale of thermalized electron transfer (∼2 ps) and a higher extraction efficiency of hot electrons (∼60%) are observed in the presence of CsPbBr3 . These observations demonstrate the potential of all-inorganic perovskite NCs in the extraction of these short-lived energy rich speciesAbstract : Harvesting of hot electrons and biexcitons from CdTe quantum dots by all-inorganic perovskite nanocrystals is demonstrated through femtosecond transient absorption measurements. Abstract : Excitation of semiconductor quantum dots (QDs) by photons possessing energy higher than the band-gap creates a hot electron–hole pair, which releases its excess energy as waste heat or under certain conditions (when hν > 2 E g ) produces multiple excitons. Extraction of these hot carriers and multiple excitons is one of the key strategies for enhancing the efficiency of QD-based photovoltaic devices. However, this is a difficult task as competing carrier cooling and relaxation of multiple excitons (through Auger recombination) are ultrafast processes. Herein, we study the potential of all-inorganic perovskite nanocrystals (NCs) of CsPbX3 (X = Cl, Br) as harvesters of these short-lived species from photo-excited CdTe QDs. The femtosecond transient absorption measurements show CsPbX3 mediated extraction of both hot and thermalized electrons of the QDs (under a low pump power) and (under a high pump fluence) extraction of multiple excitons prior to their Auger assisted recombination. A faster timescale of thermalized electron transfer (∼2 ps) and a higher extraction efficiency of hot electrons (∼60%) are observed in the presence of CsPbBr3 . These observations demonstrate the potential of all-inorganic perovskite NCs in the extraction of these short-lived energy rich species implying that complexes of the QDs and perovskite NCs are better suited for improving the efficiency of QD-sensitized solar cells. … (more)
- Is Part Of:
- Nanoscale. Volume 10:Issue 2(2018)
- Journal:
- Nanoscale
- Issue:
- Volume 10:Issue 2(2018)
- Issue Display:
- Volume 10, Issue 2 (2018)
- Year:
- 2018
- Volume:
- 10
- Issue:
- 2
- Issue Sort Value:
- 2018-0010-0002-0000
- Page Start:
- 639
- Page End:
- 645
- Publication Date:
- 2017-12-13
- Subjects:
- Nanoscience -- Periodicals
Nanotechnology -- Periodicals
620.505 - Journal URLs:
- http://www.rsc.org/Publishing/Journals/NR/Index.asp ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7nr07830g ↗
- Languages:
- English
- ISSNs:
- 2040-3364
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9830.266000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 7744.xml