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Reduced titania nanorods and Ni–Mo–S catalysts for photoelectrocatalytic water treatment and hydrogen production coupled with desalination

[Display omitted] •A novel ternary hybrid photoelectrochemical process is presented.•Thermochemically reduced TiO2 nanorod arrays are developed for treatment of urea.•Ni-Mo-S composite electrocatalysts are developed for H2 production.•The photoanodic and cathodic processes are coupled with desalinat...

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Published in:Applied catalysis. B, Environmental Environmental, 2021-05, Vol.284, p.119745, Article 119745
Main Authors: Kim, Seonghun, Han, Dong Suk, Park, Hyunwoong
Format: Article
Language:English
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Summary:[Display omitted] •A novel ternary hybrid photoelectrochemical process is presented.•Thermochemically reduced TiO2 nanorod arrays are developed for treatment of urea.•Ni-Mo-S composite electrocatalysts are developed for H2 production.•The photoanodic and cathodic processes are coupled with desalination.•The high efficiency ternary processes are achieved. This study presents a ternary hybrid solar desalination process coupled with photoelectrocatalytic water treatment and H2 production in a single device. The desalination of brackish water in the desalination cell is initiated via photoinduced charge generation with a thermochemically reduced TiO2 nanorod array photoanode. The chlorides transferred to the neighboring anolyte at ion-transport efficiency of ∼100% are photoelectrochemically transformed into reactive chlorine species responsible for the decomposition of urea into nitrate in the anolyte. Simultaneously, the H2 production with a Ni–Mo–S (Ni2S3/MoS2) composite catalyst grown onto porous Ni substrate is achieved at Faradaic efficiency of ∼90% in the catholyte concentrated with desalted Na+. Regardless of the operation condition, the H2 energy contributes to the reduction in the energy consumption for desalination by 25%–30%. The overall ternary hybrid process is understood systematically, and the physiochemical properties and electrochemical behavior of the Ni–Mo–S catalysts are examined.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2020.119745