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CdS decorated MnWO nanorod nanoheterostructures: a new 0D-1D hybrid system for enhanced photocatalytic hydrogen production under natural sunlight. | LitMetric

CdS decorated MnWO nanorod nanoheterostructures: a new 0D-1D hybrid system for enhanced photocatalytic hydrogen production under natural sunlight.

Nanoscale Adv

Nanocrystalline Laboratory, Centre for Material for Electronic Technology (CMET), Department of Information Technology, Govt. of India Panchawati, Off Pashan Road Pune 411007 India +91 20 2589 8180 +91 20 2589 9273.

Published: January 2021

Constructing a heterostructure is an effective strategy to reduce the electron-hole recombination rate, which enhances photocatalytic activity. Here, we report a facile hydrothermal method to grow CdS nanoparticles on MnWO nanorods and their photocatalytic hydrogen generation under solar light. A structural study shows the decoration of hexagonal CdS nanoparticles on monoclinic MnWO. Morphological studies based on FE-TEM analysis confirm the sensitization of CdS nanoparticles (10 nm) on MnWO nanorods of diameter-35 nm with mean length ∼100 nm. The lower PL intensity of MnWO was observed with an increasing amount of CdS nanoparticles, which shows inhibition of the charge carrier recombination rate. A CdS@MnWO narrow band gap semiconductor was employed for photocatalytic hydrogen generation from water under solar light and the highest amount of hydrogen, 3218 μmol h g, is obtained which is 21 times higher than that with pristine MnWO. The enhanced photocatalytic activity is ascribed to the formation of a CdS@MnWO nanoheterostructure resulting in efficient spatial separation of photogenerated electron-hole pairs due to vacancy defects. More significantly, direct Z-scheme electron transfer from MnWO to CdS is responsible for the enhanced hydrogen evolution. This work signifies that a CdS decorated MnWO nanoheterostructure has the potential to improve the solar to direct fuel conversion efficiency.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9418746PMC
http://dx.doi.org/10.1039/d0na00843eDOI Listing

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