
ACS Energy Letters, Journal Year: 2025, Volume and Issue: unknown, P. 2641 - 2649
Published: May 7, 2025
Language: Английский
ACS Energy Letters, Journal Year: 2025, Volume and Issue: unknown, P. 2641 - 2649
Published: May 7, 2025
Language: Английский
Journal of the American Chemical Society, Journal Year: 2025, Volume and Issue: unknown
Published: March 8, 2025
Electrochemical H2 production from water favors low-voltage molecular oxidation to replace the oxygen evolution reaction as an energy-saving and value-added approach. However, there exists a mismatch between high demand for slow anodic reactions, restricting practical applications of such hybrid systems. Here, we propose bipolar approach, with generation N–N oxidatively coupled dehydrogenation (OCD) 3,5-diamino-1H-1,2,4-triazole (DAT), in addition cathodic generation. The system requires relatively low potentials 0.872 1.108 V vs RHE reach 10 500 mA cm–2, respectively. H-type electrolyzer only 0.946 1.129 deliver 100 respectively, electricity consumption (1.3 kWh per m3 H2) reduced by 68%, compared conventional splitting. Moreover, process is highly appealing due absence traditional hazardous synthetic conditions azo compounds at anode crossover/mixing H2/O2 electrolyzer. A flow-type operates stably cm–2 300 h. Mechanistic studies reveal that Pt single atom nanoparticle (Pt1,n) optimize adsorption S active sites over Pt1,n@VS2 catalysts. At anode, stepwise −NH2 DAT then oxidative coupling −N–N– predominantly form while generating H2. present report paves new way atom-economical aminotriazole green electrosynthesis chemicals.
Language: Английский
Citations
2Science China Chemistry, Journal Year: 2025, Volume and Issue: 68(5), P. 1630 - 1631
Published: March 13, 2025
Citations
0Advanced Functional Materials, Journal Year: 2025, Volume and Issue: unknown
Published: April 24, 2025
Abstract Ni single‐atoms (SAs) are active for electrocatalytic CO 2 reduction reaction (CO RR) to CO, but their performance still needs be further improved practical implementation. Herein, a strategy of “short‐ and long‐range modulation” is reported synergistically modulate the electronic structure SAs by constructing nanoparticles (NPs) integrated with N, P‐coordinated on N‐doped carbon supports (Ni‐P 1 N 3 /Ni NPs @NC). Experiments theoretical calculations reveal that both short‐range modulation involving Ni–P coordination collectively enhance electron localization around SAs, thus increasing binding strength key * COOH intermediate. This results in an RR lowering energy barrier. Ni‐P @NC exhibits Faradaic efficiency exceeding 99.0% across wide potential range from −0.5 −1.1 V versus reversible hydrogen electrode (vs RHE), highest partial current density −544 mA cm −2 at vs RHE.
Language: Английский
Citations
0Fuel, Journal Year: 2025, Volume and Issue: 397, P. 135488 - 135488
Published: April 25, 2025
Language: Английский
Citations
0ACS Energy Letters, Journal Year: 2025, Volume and Issue: unknown, P. 2641 - 2649
Published: May 7, 2025
Language: Английский
Citations
0