Nickel-iron composites are efficient in catalyzing oxygen evolution. Here, we develop a microorganism corrosion approach to construct nickel-iron hydroxides. The anaerobic sulfate-reducing bacteria, using sulfate as the electron acceptor, play a significant role in the formation of iron sulfide decorated nickel-iron hydroxides, which exhibit excellent electrocatalytic performance for oxygen evolution. Experimental and theoretical investigations suggest that the synergistic effect between oxyhydroxides and sulfide species accounts for the high activity. This microorganism corrosion strategy not only provides efficient candidate electrocatalysts but also bridges traditional corrosion engineering and emerging electrochemical energy technologies.
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http://dx.doi.org/10.1038/s41467-020-18891-x | DOI Listing |
Adv Sci (Weinh)
January 2025
Institution Faculty of Arts and Sciences & Center for Advanced Materials Research, Beijing Normal University, Zhuhai, 519087, China.
The oxygen evolution reaction (OER) involves the recombination of diamagnetic hydroxyl (OH) or water (HO) into the paramagnetic triplet state of oxygen (O). The spin conservation of oxygen intermediates plays a crucial role in OER, however, research on spin dynamics during the catalytic process remains in its early stages. Herein, β-Ni(OH) and Fe-doped β-Ni(OH) (NiFe(OH)) are utilized as model catalysts to understand the mechanism of spin magnetic effects at iron (III) sites during OER.
View Article and Find Full Text PDFNat Commun
January 2025
National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, PR China.
Transition-metal layered double hydroxides are widely utilized as electrocatalysts for the oxygen evolution reaction (OER), undergoing dynamic transformation into active oxyhydroxides during electrochemical operation. Nonetheless, our understanding of the non-equilibrium structural changes that occur during this process remains limited. In this study, utilizing in situ energy-dispersive X-ray absorption spectroscopy and machine learning analysis, we reveal the occurrence of deprotonation and elucidate the role of incorporated iron in facilitating the transition from nickel-iron layered double hydroxide (NiFe LDH) into its active oxyhydroxide.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Dipartimento di Scienze Fisiche e Chimiche, Universita degli Studi dellAquila, Coppito, 67100 L'Aquila, Italy.
We present a comprehensive theoretical study, using state-of-the-art density functional theory simulations, of the structural and electrochemical properties of amorphous pristine and iron-doped nickel-(oxy)hydroxide catalyst films for water oxidation in alkaline solutions, referred to as NiCat and Fe:NiCat. Our simulations accurately capture the structural changes in locally ordered units, as reported by X-ray absorption spectroscopy, when the catalyst films are activated by exposure to a positive potential. We emphasize the critical role of proton-coupled electron transfer in the reversible oxidation of Ni(II) to Ni(III/IV) during this activation.
View Article and Find Full Text PDFInorg Chem
January 2025
School of Chemistry and Chemical Engineering, School of Pharmacy, Jiangsu University, Zhenjiang 212013, P. R. China.
Electrochemical water splitting is a promising method for the generation of "green hydrogen", a renewable and sustainable energy source. However, the complex, multistep synthesis processes, often involving hazardous or expensive chemicals, limit its broader adoption. Herein, a nitrate (NO) anion-intercalated nickel-iron-cerium mixed-metal (oxy)hydroxide heterostructure electrocatalyst is fabricated on nickel foam (NiFeCeOH@NF) via a simple electrodeposition method followed by cyclic voltammetry activation to enhance its surface properties.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
School of Materials Science and Engineering, CNPC-CZU Innovation Alliance, Key Laboratory of Materials Surface Science and Technology of Jiangsu Province Higher Education Institutes, Changzhou University, Changzhou, 213164, Jiangsu, China.
Herein, NiFeP/TiC@NF was synthesized from a hydrothermal process and chemical conversion, and exhibited a low overpotential of 177 mV at = 50 mA cm, a low Tafel slope of 56 mV dec, and a very competitive stable activity in alkaline electrolyte, proposing a strategy for efficient OER and overall water splitting.
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