4.7 Article

Eliciting the contribution of TiN to photoelectrochemical performance enhancement of Imma-LaTiO2N at neutral pH

Journal

MATERIALS TODAY ENERGY
Volume 27, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.mtener.2022.101053

Keywords

Oxynitrides; LaTiO2N; Titanium nitride; Water splitting; Photoelectrocatalysis

Funding

  1. European Union [793882]
  2. Marie Curie Actions (MSCA) [793882] Funding Source: Marie Curie Actions (MSCA)

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The presence of TiN in LaTiO2N material improves the photoelectrochemical performance by enhancing charge separation and transport, resulting in longer lifetimes of charge carriers.
The presence of defects, which act as the recombination hubs for photogenerated charge carriers, hinders the improvement of photocatalytic activity for oxygen evolution reaction of LaTiO2N under visible light irradiation via a four-electron-transfer reaction pathway. Here, we involve titanium nitride (TiN) in a varying content (0e17.8%) to improve the efficiency of charge separation and transport, influencing the photoelectrochemical performance of LaTiO2N. The characterization results confirm the formation of a strong contact between orthorhombic-LaTiO2N and cubic-TiN particles. The photoelectrochemical (PEC) measurements reveal the inverse dependence between electron transfer phenomena and charge carrier recombination, which allows to understand the trend when modifying LaTiO2N with TiN. In fact, the incorporation of 17.8% TiN in the LaTiO2N:TiN material results in a higher photocurrent. Open-circuit potential (OCP) decay and transient absorption spectroscopy (TAS) studies confirm longer lifetimes of charge carriers for increasing amounts of TiN in the synthesized materials. Thus, the main role of TiN is to improve the properties of the semiconductor-electrolyte interface, having verified its impact on the separation and transport of photogenerated charge carriers. Furthermore, computational studies predict that the adsorption of water molecules is favored at the LaTiO2N:TiN surface compared to the individual TiN and LaTiO2N surfaces. (C) 2022 Elsevier Ltd. All rights reserved.

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