In Situ TEM Observation of Electric Field-Directed Self-Assembly of PbS and PbSe Nanoparticles

Nano-sized particles of semiconducting lead sulfide and selenide and their 2D thin layers show high potential in applications, such as field-effect transistors, photodetectors, solar cells, and thermoelectric devices. The generation of PbS and PbSe nanobars and nanocubes is evoked by in situ electron beam treatment, leading to the formation of thin, extended 2D nanolayers. The initial single crystals are decomposed via sublimation of PbS and PbSe in terms of molecular and atomic fragments, which finally condense on the cold substrate to form nanostructures. The fragments in the gas phase were proven using mass spectrometry. In the case of PbS, Pb+ and PbS+ species could were detected, whereas PbSe disintegrated into Pb+, Se2+, and PbSe+. The threshold current that initiates fragmentation increases from PbTe via PbSe up to PbS, which is in line with the increasing crystal formation energies. The uniform orientation of independently formed nanoparticles on the macroscopic scale can be explained by an external electric field acting on emerging dipolar nanospecies. The external dipole field originates from the sputtered mother crystal, where the electron flux is initiated; thus, a current arises between the crystal’s hot and cold ends. On the contrary, in small single crystals, due to the lack of sufficient charge carriers, only local material excavation is detected instead of extended depletion and subsequent nanoparticle deposition. This fragmentation process may represent a new preparation route that provides lead chalcogenide nanofilms that are free of contamination or surfactant participation, which are typical drawbacks associated with the application of wet chemical methods.