| dc.description.abstract |
Photoelectrochemical water splitting is a greener approach to produce hydrogen (H2) as an efficient chemical fuel for the future with high energy density. However, it is extremely challenging to develop suitable semiconductor materials with desired efficiency and stability, which can be applied for practical applications. Looking at the theoretical efficiency and the solar spectrum, it is clear that visible-light-active semiconductors are the most appealing candidates. Herein, CdIn2.2Sy (CIS), a visible light-active semiconductor, is explored as a photoanode for PEC water splitting. The thin nanosheets of CIS are grown vertically through a hydrothermal method. These can efficiently absorb visible light through multiple reflections and scattering of light inside the material and enhance the light–matter interaction. As a result, the developed CIS thin nanosheets produce a maximum photocurrent density of 3.97 mA/cm2 at “1.6” V versus RHE under continuous back illumination. On the other hand, CIS attains a maximum photoconversion efficiency of ∼1.72% at “0.60” V versus RHE. Furthermore, to improve the efficiency and stability, “S” and “N” codoped C-dots (S, N-CDs) are adorned on the CIS photoanode. The “S” and “N” codoped C-dots and CIS form the type-II heterostructure, which efficiently boosts the charge separation and transportation of photogenerated electrons and holes. The transient decay time becomes longer in the case of heterostructure compared to bare CIS. The heterostructure generates 11.2 mA/cm2 photocurrent densities at an applied potential of “1.6” V versus RHE. At the same time, the heterostructure CIS/S, N-CDs-B achieves a ∼2.08-fold higher photoconversion efficiency compared to bare CIS nanosheets and is stable up to 1500 s under continuous back illumination. The present work offers an approach for designing an efficient and stable photoanode for PEC water splitting. |
en_US |