The quantum dots (QDs) are colloidal semiconductor nanocrystals whose optical and electronic properties are governed by the quantum confinement effect. When the physical dimension of the nanocrystal becomes smaller than the exciton Bohr radius, continuous energy bands split into discrete, atomic-like electronic states, allowing the effective bandgap to be precisely tuned via particle size.
Because of their nanoscale dimensions, QDs exhibit a remarkably high surface-to-volume ratio, leaving a high density of under-coordinated surface atoms that can act as deep trap states and non-radiative recombination centers. To mitigate high surface energy, prevent irreversible aggregation, and passivate these electronic trap sites, QDs are synthesized with a shell of organic capping ligands (such as long-chain fatty acids or amines).
Beyond ensuring colloidal stability and determining solubility in polar or non-polar solvents, these ligand molecules dictate the interdot distance within assembled thin films. This spacing acts as an insulating tunneling barrier that critically influences charge carrier mobility, interparticle electronic coupling, and overall optoelectronic performance in devices like light-emitting diodes and photodetectors.
As the QDs are capped with large chain organic ligands. The carrier transport in the QDs happen through hopping. So when the QDs have large ligands, the interdot spacing is high which makes the hopping of carriers difficult and reduces the conductivity. Hence, exchanging the long chain ligands with short chain ligands reduces the interdot spancing and increases the conductivity.
Replacing bulky, native long-chain organic molecules with compact inorganic ligands or short-chain species such as halides, pseudohalides, short dithiols, or amines can significantly reduce interparticle spacing in PbS quantum dot films. These short, strongly coordinating ligands effectively passivate under-coordinated surface trap states and shift the valence and conduction band energy levels, allowing precise control over work functions and band alignment. Furthermore, minimised interdot distances drastically improve charge carrier tunneling and film conductivity, which is essential for optimising injection efficiency in optoelectronic devices.
Blending two distinct populations of quantum dots, such as varying sizes or bandgaps, within a shared matrix enables the independent tailoring of absorption and emission characteristics. Within these multicomponent architectures, efficient non-radiative energy transfer pathways such as Förster Resonance Energy Transfer facilitates rapid exciton funneling from higher-energy donor quantum dots to lower-energy acceptor quantum dots. Consequently, binary blend engineering enhances carrier harvesting, reduces non-radiative recombination losses, and optimises performance in advanced light-emitting devices.