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Porous TiWO3/SrWO4 with high titanium molar ratio for efficient photoelectrocatalytic nitrogen reduction under mild conditions.
- Source :
-
Applied Catalysis B: Environmental . Feb2024, Vol. 341, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
-
Abstract
- Ammonia synthesized by nitrogen reduction is the most promising new energy material. Photoelectrocatalytic (PEC) nitrogen reduction reaction (NRR) occurs under ambient conditions and is the optimal alternative to the energy-intensive Haber-Bosch method. Here, we report the one-step reaction synthesis of Ti–WO 3 /SrWO 4 as a photocathode for ammonia synthesis. First-principles calculations demonstrate that Ti doping can afford nitrogen-adsorption sites, and Ti3+ undergoes chemical adsorption and becomes a nitrogen-activation site by providing electrons to nitrogen. Under light irradiation, the photogenerated electrons are captured by Ti4+; this is conducive to the activation and regeneration of Ti3+, thus forming a nitrogen fixation cycle and improving the nitrogen fixation yield. At − 0.5 V vs. RHE, the ammonia synthesis efficiency reaches 11.17 μg h-1 cm-2, which is four times that of SrWO 4. Furthermore, the high stability and N-gas sensitivity of Ti–WO 3 /SrWO 4 in the NRR indicate that it can be used as an efficient and stable photoelectrocatalyst for ammonia synthesis. [Display omitted] • SrWO 4 firstly utilized as an effective photoelectrocatalyst for N 2 fixation. • Ti-WO 3 /SrWO 4 was synthesized by a one-step reaction based on H 2 WO 4. • N 2 is more easily adsorbed on Ti to facilitate the NRR reaction. • Ti-WO 3 /SrWO 4 PEC synthesis of ammonia is greatly improved. [ABSTRACT FROM AUTHOR]
- Subjects :
- *NITROGEN cycle
*ELECTRON capture
*NITROGEN
*TITANIUM
*AMMONIA
*NITROGEN fixation
Subjects
Details
- Language :
- English
- ISSN :
- 09263373
- Volume :
- 341
- Database :
- Academic Search Index
- Journal :
- Applied Catalysis B: Environmental
- Publication Type :
- Academic Journal
- Accession number :
- 173173863
- Full Text :
- https://doi.org/10.1016/j.apcatb.2023.123299