Abstract

Herein, Ag-ZnO core-shell nanoparticles (NPs) with enhanced photocatalytic activity were prepared by coating Ag metal cores with ZnO semiconductor shells through atomic layer deposition (ALD). Instrumental analysis revealed that the ultra-thin and conformal nature of the shell allowed the core-shell NPs to simultaneously exploit the photocatalytic properties of ZnO and the plasmonic properties of Ag. In a rhodamine B photodegradation test performed under artificial sunlight, Ag-ZnO core-shell NPs exhibited better photocatalytic performance than other prepared photocatalysts, namely ZnO NPs and ALD-ZnO coated ZnO NPs. The performance enhancement was ascribed to the effect of noble metal-semiconductor heterojunctions, which increased the efficiency of electron-hole separation, i.e., the Ag core effectively captured excited electrons at the ZnO surface, which resulted in the elevated production of hydroxyl radicals from holes remaining at ZnO. A three-dimensional finite-difference time-domain simulation of the Ag-ZnO NPs with variable shell thickness showed that ZnO shells on Ag metal cores increase the intensity of light around NPs, allowing the plasmonic cores to fully utilize incident light.

Highlights

  • IntroductionCore-shell NPs featuring noble metal-semiconductor heterojunctions are promising materials for the solar light-induced decontamination of water [5]

  • Core-shell photocatalysts fabricated by atomic layer deposition (ALD) are expected to exhibit enhanced photocatalytic performance and increased lifetime due to the inhibitory effect of the shell on core oxidation

  • The photocatalytic activity of asfabricated Ag-ZnO core-shell NPs was determined in a rhodamine b (RhB) photodegradation test and compared to those of ZnO NPs and ALD-ZnO coated ZnO (ZnO-ZnO) NPs

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Summary

Introduction

Core-shell NPs featuring noble metal-semiconductor heterojunctions are promising materials for the solar light-induced decontamination of water [5]. Core-shell photocatalysts fabricated by ALD are expected to exhibit enhanced photocatalytic performance and increased lifetime due to the inhibitory effect of the shell on core oxidation. ZnO is a unique semiconductor photocatalyst exhibiting a wide band gap, high oxidizing strength, good eco-stability, and excellent photocatalytic performance [1,9]. The photocatalytic activity of asfabricated Ag-ZnO core-shell NPs was determined in a rhodamine b (RhB) photodegradation test and compared to those of ZnO NPs and ALD-ZnO coated ZnO (ZnO-ZnO) NPs. The light enhancement effects in the visible region induced by the LSPR of the Ag core were verified by three-dimensional (3D) finite-difference time-domain (FDTD) simulation of Ag-ZnO NPs with variable ZnO shell layer thickness

Fabrication of Ag-ZnO core-shell NPs
Instrumental characterization and photocatalytic activity determination
Results and discussion
Conclusions

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