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This study demonstrates the successful fabrication of mixed-metal CoFePBA/NF with hierarchical 1D + 3D string-bead morphology through in situ conversion, followed by sulfidation to obtain highly active s-CoFePBA/NF. The optimized s-CoFePBA/NF (500 °C) demonstrates exceptional trifunctional electrocatalytic performance, achieving ultralow overpotentials of 226 mV (OER) and 127 mV (HER) at 10 mA cm, along with a remarkable UOR potential of 1.317 V. Remarkably, the assembled s-CoFePBA/NF (500 °C)||s-CoFePBA/NF (500 °C) electrolytic cell requires only 1.60 V for overall water splitting and 1.41 V for urea-assisted water splitting at 10 mA cm, significantly outperforming the commercial IrO/NF||Pt/C/NF electrolytic cell (1.53 V). The system maintains excellent stability over 40 h of operation with ∼95% Faradaic efficiency for H production, offering an optimized strategy for urea-waer electrolysis. Therefore, this work represents an advancement in developing multifunctional electrocatalysts for sustainable hydrogen production coupled with urea wastewater treatment.
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http://dx.doi.org/10.1021/acs.inorgchem.5c02265 | DOI Listing |
Inorg Chem
June 2025
School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang 315211, PR China.
This study demonstrates the successful fabrication of mixed-metal CoFePBA/NF with hierarchical 1D + 3D string-bead morphology through in situ conversion, followed by sulfidation to obtain highly active s-CoFePBA/NF. The optimized s-CoFePBA/NF (500 °C) demonstrates exceptional trifunctional electrocatalytic performance, achieving ultralow overpotentials of 226 mV (OER) and 127 mV (HER) at 10 mA cm, along with a remarkable UOR potential of 1.317 V.
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