Semiconductor colloidal quantum dots (QDs) of CdTe and alloyed Cd x Zn1−x Te QDs with N-acetyl-L-cysteine capping ligands are synthesized by a reflux method in aqueous solution. Alloying provides a new degree of freedom to tune the optical and electronic properties of the nanocrystals. The photoluminescence (PL) of Cd x Zn1−x Te QDs is sharper and displays a highly enhanced quantum yield (QY) of 65% relative to the 16% of CdTe QDs. The fluorescence of Cd x Zn1−x Te QDs is observed to be highly stable for over 12 months without degradation, while that of CdTe QDs begins to mildly flocculate around 8 months of storage. To characterise the material structure and composition, UV-Vis absorption spectroscopy, x-ray powder diffraction, transmission electron microscopy, and inductively coupled plasma mass spectrometry measurements are carried out. To understand the fundamental processes that play in the luminescence behaviour, temperature- and size-dependent PL spectra are investigated in the range 80–300 K. The Varshni and O’Donnell equations fit well on the PL peak emission energies and the Huang–Rhys parameter indicates the strengthening of exciton–phonon coupling in the nanocrystals upon alloying and with decreasing nanocrystal sizes. PL linewidth analysis reveals that the inhomogeneous broadening is considerably reduced in Cd x Zn1−x Te QDs relative to CdTe. Moreover, the quantum confinement effect of the nanocrystals leads to an increase in exciton–acoustic phonon interactions with the coefficients ranging between 26.9 and 95.6 µeV K−1 compared to the bulk CdTe value of 0.72 µeV K−1. Exciton–longitudinal optical phonon interactions are made stronger by the ZnTe alloying with the coefficients lying in the range between 24.8 and 41.7 meV and also with the effect of increasing crystal size. An Arrhenius plot of PL integrated area is used to calculate the thermal activation energy value E a of the non-radiative recombination channel, which is 132 meV for CdTe QDs and a higher value of 185 meV for Cd x Zn1−x Te QDs. This is consistent with the observed QY enhancement in Cd x Zn1−x Te QDs as a higher E a value indicates reduced generation of non-radiative recombination centres and a decrease in defect densities upon alloying. Cd x Zn1−x Te QDs with enhanced fluorescence properties serve both as a medium for studying fundamental effects of alloying and its properties, and for practical applications such as biomedical labelling and optoelectronics.
Semiconductor quantum dots (QDs) are emerging as the forefront alternative for the conventional imaging technology, particularly in infrared region from near infrared (0.75–1.4 μm) to long-wave infrared (8–14 μm) region. A handful of materials are explored for mid infrared imaging QDs and they are all invariably binary semiconductor compounds. Ternary alloyed quantum dots in many previous cases have shown properties that are unique and better than parent binary compounds. In this work, we have synthesized ternary alloyed HgCdTe quantum dots and studied their photophysical properties. Previously studied ternary alloyed HgCdTe CQDs absorb and emit in regions limited upto near-infrared region. We have tuned the excitonic absorption of HgCdTe QDs in the range of 2.2–5 μm, where addition of cadmium clearly showed blueshift in excitonic peak as compared to that of HgTe QDs. Structural properties are studied by TEM, XRD & XPS techniques. Electrical behaviour is studied by measuring I-V, I-V-T curves. Photodetectors are fabricated in photoconductive geometry showing promising photo-response under visible (532 nm) and NIR (810 nm, 1550 nm) excitation. Responsivity of the devices is in the order of 1 mA W−1 at 1 V bias and show good linearity over irradiance range of 0.025 and 2.5 W cm−2. These results pave the way for development of next generation cost-effective short-wave and mid-wave infrared region optoelectronic devices based on narrow bandgap HgCdTe nanocrystals.
Background: Omega-3 fatty acid (OM3) intake is associated with a lower risk of developing Alzheimer’s disease, but individuals carrying the ɛ4 allele of apolipoprotein E (APOE4) might not benefit from this prevention strategy. Indeed, they might have lower OM3 into plasma free fatty acid (FFA) and lysophosphatidylcholine (LPC) compartments, the two forms the brain can take-in. Objective: To evaluate the docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) concentrations in the FFA and LPC pre- and post OM3 supplementation in APOE4 carriers and non-carriers. BDesign: Plasma samples from 25 APOE4 carriers and non-carriers before and six months after receiving 2.5 g/d DHA+EPA daily were analyzed. DHA and EPA concentrations in the LPC, and FFA were compared by supplementation and genotype. A secondary analysis investigated the interaction between body mass index (BMI) and APOE genotype status. Results: There was no genotype x supplement interaction nor a genotype effect on LPC and FFA. However, there was a supplement effect where OM3 increased in all lipid compartment by < 1-fold to 4-fold. Individuals with a low BMI had higher OM3 increase concentrations in the LPC than those with a high BMI. Conclusions: APOE4 carriers and non-carriers can both benefit from taking an OM3 supplement. However, individuals with a high BMI have lower OM3 increases than those with a lower BMI.
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