Issue 31, 2022

Azide molecule mediated electrolyte engineering for selective photoelectrochemical azo coupling and efficient and stable water splitting

Abstract

Low-performance and instability severely limit photoelectrochemical (PEC) water splitting and organic synthesis of photoanodes. Electrolyte regulation as a facile and scalable route receives less attention, and always requires oxygen evolution catalysts (OECs). Herein, we report azide molecule mediated electrolyte regulation to achieve OEC-free selective PEC reactions over a BiVO4 (BVO) photoanode. pH-sensitive 5-aminotetrazolium (5AT) acts as not only a substrate for the PEC azo coupling reaction but also a “liquid phase cocatalyst” to substantially facilitate charge transfer at the photoanode-electrolyte interface. In 5AT/Na2SO4 electrolyte, the azo coupling reaction occurs at pH > 4, whereas the water splitting reaction takes place at pH < 4, and polyaniline passivated BVO (BVO-PANI) exhibits a photocurrent density of 4.22 mA cm−2 at 1.23 VRHE with an onset potential of 0.34 VRHE and stable photocurrent density for 4 h. Meanwhile, 5AT as a “liquid phase cocatalyst” is universal for a variety of photoanodes, such as α-Fe2O3. Further, 5AT/NaVO3/Na2SO4 ternary electrolyte solution allows BVO-PANI to exhibit a photocurrent density of 5.1 mA cm−2 at 1.23 VRHE with an onset potential of 0.27 VRHE and stable PEC performance for 10 h. This work opens up a new avenue of electrolyte regulation to promote PEC performance and stability of photoanodes.

Graphical abstract: Azide molecule mediated electrolyte engineering for selective photoelectrochemical azo coupling and efficient and stable water splitting

Supplementary files

Article information

Article type
Paper
Submitted
08 Jun 2022
Accepted
14 Jul 2022
First published
14 Jul 2022

J. Mater. Chem. A, 2022,10, 16646-16654

Azide molecule mediated electrolyte engineering for selective photoelectrochemical azo coupling and efficient and stable water splitting

S. Li, M. Li, F. Chen and H. Huang, J. Mater. Chem. A, 2022, 10, 16646 DOI: 10.1039/D2TA04559A

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