Abstract:Charge and energy transfer dynamics in Colloidal CdSeTe/ZnS quantum dots (QDs)/monolayer molybdenum disulfide (MoS2) heterostructures have been investigated by time-resolved single-dot photoluminescence (PL) spectroscopy. Time-gated method is used to separate...
“…There was obvious spectral overlap between the absorption spectrum of WS 2 and the emission spectrum of CQDs (see Figure S7). It was suggested that PL quenching of CQDs may originate from the energy transfer between CQD–WS 2 composites. – Energy transfer efficiency (η) can be calculated by below formula – η=kETkr+knr+kET=I0−II0where I 0 and I is the PL intensity at the peak of 490 nm of CQDs alone and the CQD–WS 2 composites. k r and k nr are the radiative and nonradiative recombination rates of photogenerated excitons, which are intrinsic properties of CQDs that are unaffected by WS 2 .…”
The combination of carbon quantum dots (CQDs) with transition
metal
disulfides results in 0D–2D composites with enhanced light
absorption properties. In the transient absorption spectrum of CQD–WS2 composites, photoinduced absorption feature of the intrinsic
state was inhibited by WS2. The suppressed photoinduced
absorption feature of the defect state appeared at a particular WS2 concentration (0.1–0.13 mg/mL), which indicates that
the capture ability of the defect state is enhanced by WS2. Transient absorption spectrum reveals the energy transfer dynamics
from intrinsic and defect states of CQDs to WS2. Energy
transfer efficiency can reach up to 92% at 0.2 mg/mL WS2. The understanding and manipulation of energy transfer dynamics
in 0D–2D composites has made great contributions in optical
devices.
“…There was obvious spectral overlap between the absorption spectrum of WS 2 and the emission spectrum of CQDs (see Figure S7). It was suggested that PL quenching of CQDs may originate from the energy transfer between CQD–WS 2 composites. – Energy transfer efficiency (η) can be calculated by below formula – η=kETkr+knr+kET=I0−II0where I 0 and I is the PL intensity at the peak of 490 nm of CQDs alone and the CQD–WS 2 composites. k r and k nr are the radiative and nonradiative recombination rates of photogenerated excitons, which are intrinsic properties of CQDs that are unaffected by WS 2 .…”
The combination of carbon quantum dots (CQDs) with transition
metal
disulfides results in 0D–2D composites with enhanced light
absorption properties. In the transient absorption spectrum of CQD–WS2 composites, photoinduced absorption feature of the intrinsic
state was inhibited by WS2. The suppressed photoinduced
absorption feature of the defect state appeared at a particular WS2 concentration (0.1–0.13 mg/mL), which indicates that
the capture ability of the defect state is enhanced by WS2. Transient absorption spectrum reveals the energy transfer dynamics
from intrinsic and defect states of CQDs to WS2. Energy
transfer efficiency can reach up to 92% at 0.2 mg/mL WS2. The understanding and manipulation of energy transfer dynamics
in 0D–2D composites has made great contributions in optical
devices.
“…The potential mechanisms behind the observed PL enhancement include photoexcited CT and Förster resonance energy transfer (FRET). [38] Si QDs exhibit a longer luminescent decay time (%μs) due to their quasi-direct-bandgap nature with indirect-gap properties, which may rule out the possibility of FRET due to unfavorable harmonics between light decay and subsequent absorption. [39][40][41][42] Therefore, we attribute the dominant mechanism of PL enhancement to CT following the decoration of Si QDs.…”
Hybrid 2D/0D structures with various 2D materials and 0D quantum dots (QDs) have been studied to overcome the limitations of 2D materials. We develop a hybrid structure with MoS2 and silicon quantum dots (Si QDs) as a photodetector. I‐V transfer characteristics show the threshold voltage shift after decorating Si QDs on MoS2, which results from n‐type doping effect to the MoS2 channel from Si QDs. The field‐effect mobility of the MoS2/Si QDs device is increased by ∽5.8 times compared with that of the bare MoS2 device. We understand that the mobility enhancement is attributed to the surface defect passivation of MoS2 at the interface with Si QDs. We observe that the photoresponsivity of the structure MoS2/Si QDs was improved by ∽7.7 times compared with that of the bare MoS2 device under 500 nm illumination. Additionally, we observe that the photoluminescence (PL) intensity of MoS2 is increased about 4.5 times after decoration of Si QDs. We interpret the band alignment as the type I at the interface between Si QDs and MoS2. The mobility enhancement and the photoexcited charge transfer (CT) between MoS2 and Si QDs due to the illumination lead to enhancing the photoresponsivity of the MoS2/Si QDs hybrid structure.This article is protected by copyright. All rights reserved.
“…Many other antenna systems have demonstrated extremely high energy transfer efficiencies such as photosynthetic antenna complexes and light harvesting nanotubes. , The energy concentration from large area 2D to 0D semiconductors of the same composition, however, has not been previously explored to our knowledge. It has been shown from 2D TMDs to separately synthesized nanocrystals such as WS 2 to PbS-CdS, WS 2 to CdSe/ZnS, and MoS 2 to CdSeTe/ZnS, as well as in InGaAs quantum wells to CdSe/ZnS QDs. ,,, In NPLs, energy transfer from 2D to 0D has been demonstrated from CdSe NPL to metallic nanoparticles such as Pt, Pd, and Au. ,,, Similarly, energy transfer from 2D NPLs to molecular chromophores has been demonstrated such as in 3 ML CdSe NPLs to conjugated fluorophores . These results are summarized in Figure b, where the QE is shown as a function of acceptor density (or the number of reported acceptors per area of donor).…”
Section: In Situ Grown Hgte Npl/qd Heterostructurementioning
confidence: 99%
“…Finally, in Figure 5 we compare the theoretical diffusion constant (indicated by an asterisk) to 27,28 oligoacene triplets and singlets, 29 nanotubes, 30−32 2D semiconductors, 33−40 and nanoplatelets 41,42 at room temperature. b) Energy transfer efficiency rates for 2D to 0D systems including TMDs and quantum well (QW) to NCs, 3,43,44 NPLs to NCs, 18,45 our and NPLs to conjugated fluorophores. 46 The Journal of Physical Chemistry Letters Many other antenna systems have demonstrated extremely high energy transfer efficiencies such as photosynthetic antenna complexes and light harvesting nanotubes.…”
Section: The Journal Ofmentioning
confidence: 99%
“…It has been shown from 2D TMDs to separately synthesized nanocrystals such as WS 2 to PbS-CdS, WS 2 to CdSe/ZnS, and MoS 2 to CdSeTe/ZnS, as well as in InGaAs quantum wells to CdSe/ZnS QDs. 3,43,44,50 In NPLs, energy transfer from 2D to 0D has been demonstrated from CdSe NPL to metallic nanoparticles such as Pt, Pd, and Au. 18,45,51,52 Similarly, energy transfer from 2D NPLs to molecular chromophores has been demonstrated such as in 3 ML CdSe NPLs to conjugated fluorophores.…”
Large area absorbers with localized defect emission are of interest for energy concentration via the antenna effect. Transfer between 2D and 0D quantum-confined structures is advantageous as it affords maximal lateral area antennas with continuously tunable emission. We report the quantum efficiency of energy transfer in in situ grown HgTe nanoplatelet (NPL)/quantum dot (QD) heterostructures to be near unity (>85%), while energy transfer in separately synthesized and well separated solutions of HgTe NPLs to QDs only reaches 47 ± 11% at considerably higher QD concentrations. Using Kinetic Monte Carlo simulations, we estimate an exciton diffusion constant of 1−10 cm 2 /s in HgTe NPLs, the same magnitude as that of 2D semiconductors. We also simulate in-solution energy transfer between NPLs and QDs, recovering an R −4 dependence consistent with 2D-0D near-field energy transfer even in randomly distributed NPL/QD mixtures. This highlights the advantage of NPLs 2D morphology and the efficiency of NPL/QD heterostructures and mixtures for energy harvesting.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.