4.8 Article

Photoenhanced Degradation of Sarin at Cu/TiO2 Composite Aerogels: Roles of Bandgap Excitation and Surface Plasmon Excitation

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 10, Pages 12550-12561

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c21988

Keywords

chemical warfare agent decomposition; aerogels; plasmonic photochemistry; copper nanoparticles; sarin; in situ DRIFTS

Funding

  1. Defense Threat Reduction Agency (DTRA) [HDTRA1032887 CB10300]
  2. National Research Council through a Naval Research Laboratory/National Research Council Postdoctoral Associateship

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Cu/TiO2 aerogels show high efficiency in degrading organophosphorus chemical warfare agent sarin under both dark and illuminated conditions, with more thorough mineralization of products under broadband illumination.
Multifunctional composites that couple high-capacity adsorbents with catalytic nanoparticles (NPs) offer a promising route toward the degradation of organophosphorus pollutants or chemical warfare agents (CWAs). We couple mesoporous TiO2 aerogels with plasmonic Cu nanoparticles (Cu/TiO2) and characterize the degradation of the organophosphorus CWA sarin under both dark and illuminated conditions. Cu/TiO2 aerogels combine high dark degradation rates, which are facilitated by hydrolytically active sites at the Cu parallel to TiO2 interface, with photoenhanced degradation courtesy of semiconducting TiO2 and the surface plasmon resonance (SPR) of the Cu nanoparticles. The TiO2 aerogel provides a high surface area for sarin binding (155 m(2) g(-1)), while the addition of Cu NPs increases the abundance of hydrolytically active OH sites. Degradation is accelerated on TiO2 and Cu/TiO2 aerogels with O-2. Under broadband illumination, which excites the TiO2 bandgap and the Cu SPR, sarin degradation accelerates, and the products are more fully mineralized compared to those of the dark reaction. With O-2 and broadband illumination, oxidation products are observed on the Cu/TiO2 aerogels as the hydrolysis products subsequently oxidize. In contrast, the photodegradation of sarin on TiO2 is limited by its slow initial hydrolysis, which limits the subsequent photooxidation. Accelerated hydrolysis occurs on Cu/TiO2 aerogels under visible illumination (>480 nm) that excites the Cu SPR but not the TiO2 bandgap, confirming that the Cu SPR excitation contributes to the broadband-driven activity. The high hydrolytic activity of the Cu/TiO2 aerogels combined with the photoactivity upon TiO2 bandgap excitation and Cu SPR excitation is a potent combination of hydrolysis and oxidation that enables the substantial chemical degradation of organophorphorus compounds.

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