AI Article Synopsis

  • Nanocrystalline undoped and chromium-doped PbS thin films were fabricated using a chemical bath deposition technique, revealing a polycrystalline cubic structure with a preferred growth orientation.
  • Incorporating chromium reduces the crystallite size of PbS from about 60 nm to 38 nm, while increasing strain and dislocation density; morphological analysis shows smaller nanocluster sizes with higher chromium concentrations.
  • The optical band gap increases with chromium doping, and the Cr-doped PbS electrodes exhibit improved photoelectrochemical properties, including optimized efficiencies and high stability in a sodium sulfate electrolyte solution.

Article Abstract

Nanocrystalline undoped and Cr-doped PbS thin films were prepared on glass substrates by a simple chemical bath deposition method. The X-ray diffraction analyses of the films showed their polycrystalline nature with cubic structure and preferential growth along the (111) orientation. Cr incorporation decreases the average PbS crystallite size from 59.97 to 37.59 nm, whereas the strain and dislocation density showed an increasing trend. The atomic ratio of doping for Cr is about 0.63, 1.75, and 4.70% according to energy-dispersive X-ray (EDX) spectroscopy. Morphological analysis showed that the average sizes of nanoclusters decreased from 73 to 41 nm as the Cr concentration increased. The optical band gap values are increased with increasing Cr doping. The photoelectrochemical (PEC) behaviors and the stability of the Cr doped PbS photoelectrodes were studied in 0.3 M NaSO electrolyte solution. Also, the incident photon-to-current efficiency and applied bias photon-to-current efficiency are calculated and showed optimized values of 13.5% and 1.44% at 0.68 V and 390 nm. Moreover, the optimized electrode shows high chemical stability and a long lifetime. Finally, the effect of temperature on the PEC behaviors is evaluated and the different thermodynamic parameters are calculated.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051943PMC
http://dx.doi.org/10.1039/c9ra11042aDOI Listing

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