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Developing highly-efficient and robust bifunctional electrocatalyst for overall water splitting (OWS) is desirable, but it confronts long-term challenge in the local structural reconstruction of catalyst during the hydrogen and oxygen evolution reaction (HER and OER). As inspired by the stable acid-base buffer system in human life, here we construct an electron buffer system to well address the key issue of structural reconstruction, in which the charge-buffered fullerene renders Ru-based active species to be reversibly shuttled between Ru and RuO during HER and OER. Consequently, the as-prepared Ru-RuO/C catalyst exhibits overpotentials of merely 7 and 194 mV at 10 mA cm for HER and OER in alkaline conditions, respectively. The photovoltaic-driven OWS device with a solar-to-hydrogen (STH) efficiency of 18.9% and an anion exchange membrane water electrolysis (AEMWE) system with good robustness was fabricated based on Ru-RuO/C . It was unraveled by in situ/operando spectroscopy and theoretical calculation that the significantly promoted performance of water electrolysis benefits from the fullerene-based electron shuttle effect on inhibition of structural reconstruction and electronic structural modulation of active sites as well as adsorption energy of the reaction intermediates. Our work may open an avenue to develop efficient and robust bifunctional electrocatalyst for promising industrial water electrolysis.
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http://dx.doi.org/10.1002/anie.202503608 | DOI Listing |
J Colloid Interface Sci
September 2025
State Key Laboratory of Heavy Oil Processing, College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao 266580, China.
Reaction intermediates (RI) are key factors that directly determine the efficiency of the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). In this study, a local electric field microenvironment was built in a FeNi and MoNi heterostructure (H-FeNiMo/NMF) to induce the redistribution of hydroxyls and protons on the metal sites during the OER and HER. H-FeNiMo/NMF requires only 270 and 155 mV to reach 100 mA cm in alkaline media for OER and HER, respectively.
View Article and Find Full Text PDFDalton Trans
September 2025
Sun Yat-Sen University, MOE Laboratory of Polymeric Composite and Functional Materials, School of Materials Science and Engineering, Guangzhou 510275, China.
The main bottleneck faced by traditional hydrogen production technology through water electrolysis lies in the high energy consumption of the anodic oxygen evolution reaction (OER). Combining the thermodynamically favorable ethanol oxidation reaction (EOR) with the hydrogen evolution reaction provides a promising route to reduce the energy consumption of hydrogen production and generate high value-added products. In this study, a facile method was developed for nickel oxyhydroxide (NiOOH) fabrication.
View Article and Find Full Text PDFChem Rec
September 2025
School of Chemistry and Chemical Engineering, Southeast University, Nanjing, Jiangsu, 211189, China.
Water electrolysis for hydrogen production has become an industrial focus in the era of green chemistry due to its high purity of hydrogen production and environmentally friendly, efficient process. As the half reaction of water splitting at the anode, the oxygen evolution reaction (OER) features a complex and sluggish process that restricts the efficiency of water splitting. The mechanism of OER varies with different electrolytes.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Surface Science Laboratory, Department of Materials and Geosciences, Technical University of Darmstadt, Peter-Grünberg-Straße 4, 64287 Darmstadt, Germany.
The performance of NiO-based electrocatalysts for the oxygen evolution reaction (OER) is strongly influenced by the interface between the metal support (current collector) and the catalyst layer, which modulates electronic properties and electrochemical activity. This study systematically investigates the solid-solid interface behavior of NiO thin films prepared by reactive magnetron sputtering on Pt, Au, and Ni, followed by electrochemical characterization. Stepwise NiO deposition and X-ray photoelectron spectroscopy reveal distinct band alignment and electronic structure differences at the metal-catalyst interface.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Advanced Catalysis and Green Manufacturing Collaborative Innovation Center, Changzhou University, Changzhou 213164, P. R. China.
The development of high-performance, cost-effective non-noble metal catalysts for the oxygen evolution reaction (OER) is critical to advancing sustainable hydrogen production via water electrolysis. Herein, we report a facile and mild strategy for synthesizing amorphous bimetallic organic framework materials (NiFe-MOFs) using pyridine-modified threonine (l-PyThr) as an organic ligand. The optimized NiFe-PyThr-4:1 catalyst exhibits remarkable OER activity, requiring low overpotentials of only 162 and 222 mV to achieve current densities of 10 and 100 mA cm, respectively, along with a small Tafel slope of 34.
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