Dual photoluminescence peaks observed during the synthesis of colloidal PbS nanosheets reveal their growth mechanism - two-dimensional attachments of the quantum dots. Well-grown nanosheets show the photoluminescence linewidth of 95 meV at room temperature. Aged nanosheets in toluene have enhanced photoluminescence with intensity improved by an order of magnitude.
By changing the precursor lead-to-sulfur molar ratio in the synthesis of colloidal PbS nanosheets, the lateral size of the nanosheet can be tuned in a wide range from 100 nm to 1500 nm while keeping its thickness around 2.4 nm. Using chloroalkane molecules with a long carbon-chain as the capping ligands can further reduce the lateral size down to 20 nm. The concentration of the chloroalkane in the reaction solution and the reaction temperature also have significant effects on the lateral size. At room temperature, nanosheets with a small lateral size exhibit a narrow light-emission linewidth. The same nanosheets also show a sharp exciton peak near the band edge in the optical absorption spectrum.[a] Dr.
Charged facets of a nanocrystal can form an intrinsic nanometer-size electric dipole. When the spacing between these nano dipoles is adjusted, the dipolar interaction energy is tuned from a fraction to a multiple of the thermal energy. Consequently, the onedimensional oriented attachment can be switched on or off, as is the growth of nanorods. This kinetically controlled growth is achieved at relatively low reaction temperatures while the thermodynamically controlled growth dominates at higher temperatures. The synthesized PbSe nanorods are branchless, exhibiting a single-exponential photoluminescence decay trace with an e-folding lifetime of 1.3 μs and a photoluminescence quantum yield of 35%.
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