NiFe layered double hydroxides (LDHs) are state-of-the-art catalysts for the oxygen evolution reaction (OER) in alkaline media, yet they still face significant overpotentials. Here, quantitative boron (B) doping is introduced in NiFe LDHs (ranging from 0% to 20.3%) to effectively tailor the Ni-Fe-B electronic interactions for enhanced OER performance. The co-hydrolysis synthesis approach synchronizes the hydrolysis rates of Ni and Fe precursors with the formation rate of B─O─M (M: Ni, Fe) bonds, ensuring precise B doping into the NiFe LDHs. It is demonstrated that B, as an electron-deficient element, acts as an "electron sink" at doping levels from 0% to 13.5%, facilitating the transition of Ni to the active Ni, thereby accelerating OER kinetics. However, excessive B doping (13.5-20.3%) effectively generates oxygen vacancies in the LDHs, which increases electron density at Ni sites and hinders their transition to Ni, thereby reducing OER activity. Optimal OER performance is achieved at a B doping level of 13.5%, with an overpotential of only 208 mV to reach a current density of 500 mA cm, placing it among the most effective OER catalysts to date. This Ni-Fe-B electronic engineering opens new avenues for developing highly efficient anode catalysts for water-splitting hydrogen production.
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http://dx.doi.org/10.1002/smll.202407564 | DOI Listing |
J Colloid Interface Sci
February 2025
Chongqing Key Laboratory of Photo-Electric Functional Materials, College of Physics and Electronic Engineering, Chongqing Normal University, Chongqing 401331, China. Electronic address:
Amorphous electrocatalysts display several unique advantages in electricity-driven water splitting compared to their crystalline analogs, but understanding their structure-activity relationships remains a major challenge. Herein, we show that the d- and p-electronic states of amorphous Ni-Fe-B can be subtly manipulated by varying the Ni and Fe contents. The optimal Ni-Fe-B alloy exhibits a high performance in the oxygen evolution reaction (OER), as supported by its impressive stability (no clear degradation after 100 h) and considerably lower overpotential compared to those of its crystalline analogs.
View Article and Find Full Text PDFSmall
December 2024
State Key Laboratory of Multiphase Flow in Power Engineering, Frontier Institute of Science and Technology, Xi'an Jiaotong University, Xi'an, 710049, China.
RSC Adv
July 2018
School of Environmental Science and Engineering, Hebei University of Science and Technology Shi Jiazhuang 050018 China
A hollow Ni-Fe-B nanochain is successfully synthesized by a galvanic replacement method using a Fe-B nanocomposite and a NiCl solution as the template and additional reagent, respectively. Both the concentration of Ni and the morphology of the resulting Ni-Fe-B alloy are controlled by varying the duration of the replacement process during the synthesis. The Ni-Fe-B sample synthesized for 60 min (Ni-Fe-B-60) shows the best catalytic activity at 313 K, with a hydrogen production rate of 4320 mL min g and an activation energy for the NaBH hydrolysis reaction of 33.
View Article and Find Full Text PDFJ Phys Chem A
March 2013
Key Laboratory of Soft Chemistry and Functional Materials of MOE, School of Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, PR China.
The adsorption and reaction of H2O molecule on neutral X-centered icosahedronal Al12X clusters (X = Al, Mg, Zn, Ga, Ni, Fe, B, C, Si, P) were investigated by PW91, PBE, and PWC methods. Reaction energies and reaction barriers were determined. The spin states and the doped atoms have important influences on the Al12X geometries, density, electronic properties, and energy density of reaction between Al12X with a single H2O molecule.
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