A bifunctional CoNi alloy for electrocatalytically coupled cathodic nitrate reduction and anodic HPAM oxidation
The construction of electrocatalytic cathodic nitrate reduction and anodic polyacrylamide (HPAM) oxidation reactions is a promising new electrocatalytic reaction system, which promises simultaneous ammonia synthesis and HPAM degradation. Here, we synthesised an N-doped C nanotube-encapsulated CoNi nano-alloy and used it for electrocatalytic NO 3 − reduction and HPAM oxidation reactions. Therein, CoNi-0.5 could achieve the maximum ammonia yield and Faraday efficiency of 5516.73 ± 66.07 μg h −1 mg cat −1 and 94.71 ± 1.21 %, respectively. Meanwhile, the maximum degradation rate of HPAM was 73.02 ± 1.16 % at 2 h. By In-situ ATR-SEIRAS, in-situ DEMS demonstrated that *NOH is an important reaction intermediate in the ammonia synthesis process, and the bimetallic CoNi alloy can effectively reduce the reaction energy barrier for NO 3 − reduction. This work presents a new strategy for constructing a coupled system for electrocatalytic NO 3 − reduction. • Bifunctional CoNi-x (x = 0.5,1 and 2) nano-alloy electrocatalysts • Electrocatalytic cathodic nitrate reduction coupled to anodic PAM oxidation • Reaction pathways and reaction intermediates are detected by in-situ ATR-SEIRAS, in-situ DEMS . • Revealing kinetic processes and rate-determining steps in NO 3 RR.
Authors
- Yu Fu (ORCID: https://orcid.org/0000-0002-8960-5000)
- Saule Aidarova (ORCID: https://orcid.org/0000-0001-5115-5879)
- Shu‐Jun Liu (ORCID: https://orcid.org/0000-0002-6004-9733)
- Lijie Qi (ORCID: https://orcid.org/0009-0009-7846-9507)
- Hongbin Yang (ORCID: https://orcid.org/0009-0006-8944-0062)
Institutions
- Kazakh-British Technical University (KZ)
- Shenyang Fire Research Institute (CN)
- China University of Petroleum, East China (CN)
Publication Details
- Journal
- Journal of Electroanalytical Chemistry
- Published
- 2025-04-04
- DOI
- https://doi.org/10.1016/j.jelechem.2025.119105
- Primary Topic
- Electrocatalysts for Energy Conversion
- Type
- article
- Field-Weighted Citation Impact
- 0.00