4.5 Article

Enhancing the Hydrogen Evolution Properties of Kesterite Absorber by Si-Doping in the Surface of CZTS Thin Film

Journal

ADVANCED MATERIALS INTERFACES
Volume 8, Issue 10, Pages -

Publisher

WILEY
DOI: 10.1002/admi.202002124

Keywords

CZTS; heterostructures; photocathodes; photocurrent; Si‐ doping; water splitting

Funding

  1. DST
  2. Schlumberger chair professorship
  3. DST-FIST Raman facility
  4. Academy of Finland

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Si-doping in Cu2ZnSnS4 thin film significantly affects the surface and electronic properties, resulting in band bending inversion at grain boundaries and upward shift of Fermi level. Coating with CdS and ZnO layers over Si-doped CZTS enhances photocurrent and reduces charge transfer resistance at the semiconductor-electrolyte interface.
In this work, the effects of Si-doping in Cu2ZnSnS4 are examined computationally and experimentally. The density functional theory calculations show that an increasing concentration of Si (from x = 0 to x = 1) yields a band gap rise due to shifting of the conduction band minimum towards higher energy states in the Cu2Zn(Sn1-xSix)S-4. CZTSiS thin film prepared by co-sputtering process shows Cu2Zn(Sn1-xSix)S-4 (Si-rich) and Cu2ZnSnS4 (S-rich) kesterite phases on the surface and in the bulk of the sample, respectively. A significant change in surface electronic properties is observed in CZTSiS thin film. Si-doping in CZTS inverts the band bending at grain-boundaries from downward to upward and the Fermi level of CZTSiS shifts upward. Further, the coating of the CdS and ZnO layer improves the photocurrent to approximate to 5.57 mA cm(-2) at -0.41 V-RHE in the CZTSiS/CdS/ZnO sample, which is 2.39 times higher than that of pure CZTS. The flat band potential increases from CZTS approximate to 0.43 V-RHE to CZTSiS/CdS/ZnO approximate to 1.31 V-RHE indicating the faster carrier separation process at the electrode-electrolyte interface in the latter sample. CdS/ZnO layers over CZTSiS significantly reduce the charge transfer resistance at the semiconductor-electrolyte interface.

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