gated imaging and nanocrystals-Katherine Flashcards
fingerprint treatments
long emission lifetime
sharp emission profiles
lanthanides absorb light with low efficiency, they are sensitised using an organic chromophore as ligand
absorbed energy is transferred to the lanthanide which then emits light
gated imaging in 1979
fingerprint treatment leads to a luminescence lifetime substantially longer than a nanosecond, then turn on the imaging device after light source cut-off, with a delay such that the background fluorescence has already decayed, but luminescence is continuing
position of the camera defined the gate delay
fingerprint dusted with a powder terbium complex which luminesces with a lifetime on the order of a millisecond
limited in the speed of rotation of the cylinder, limits to fingerprint treatments that yield very long lifetimes
cannot arbitrarily scale up the size of the cylinder, as eventually the distance between camera and sample becomes too large to get good image resolution
gated imaging mid 1980s
proximity-focused microchannel plate image intensifiers (MCP)
electronically turned on and off very rapidly, in times on the order of 10-8 seconds
photoluminescent semiconductor nanocrystals
CdSe nanocrystals capped with zinc sulfide to reduce aggregation of the nanocrystals
bind to amino acids in fingerprint residue
formulation for CdSe/ZnS/carboxylate functionalised nanocrystals
1uM of CdSe/ZnS/carboxylate functionalised nanocrystals left for 24 hours in solution
excitation from the ultraviolet to the red, which gives greater flexibility in terms of the excitation light source
sharp red luminescence was shown at 635nm
absorption and emission spectra
absorption spectra of nanocomposites extremely broad, similar to bulk semiconductors
fluorescent CdSe/ZnS stablised by octadecaneamine
fingermarks on silicon wafers or paper were immersed in a petroleum ether solution of CdSe/ZnS
detailed fluorescent prints were obtained on the silicon wafer specimens but fingermarks were not observed on paper due to heavy background fluorescence under UV illumination
dendrimers
repetitively branched molecules
symmetric around the core, often adopts a spherical three-dimensional morphology
dendrimers separate and trap the nanoparticles limiting their aggression size
by controlling the chemical structure and size of the dendrimers, different size nanoclusters can be prepared
nanoclusters
nanoclusters tailored by size to have luminescences ranging from blue to red, with sharp fluorescence peaks
by tailoring the size of the cluster, the luminescence lifetime is also altered but it remains in a range suitable for time-resolved work
CdS/generation 4 dendrimer solutions can be made up in methanol
absorption spectra indicated CdS nanocluster sizes of about 2.5nm
diiminde enhancement
bonding of lipids of fingerprint material, to amine functional groups of dendrimers to form the amide linkage does not occur easily
diimides convert the carboxylic acid to an ester that more readily reacts with the amine functional group of the dendrimer