Metal phosphate-type compounds have been utilized in diverse applications, and their distinctive chemical properties have recently opened avenues for their use as catalysts. Metal phosphates have previously demonstrated significant electrocatalytic activity for the anodic oxygen evolution reaction (OER) in electrochemical water splitting. However, the critical factors influencing OER electrocatalysis on Ni-based phosphates have been insufficiently explored. We herein demonstrate nickel (Ni)-based phosphates-monoclinic Ni(PO), monoclinic NiPO, and monoclinic NiPO-as exemplary materials exhibiting outstanding OER activity in alkaline media. These Ni-based phosphates exhibit superior OER overpotentials compared to conventional Ni-based oxides (NiO) and phosphides (NiP). Additionally, their OER-specific activity surpasses that of the rare metal-based benchmark, IrO, and previously reported state-of-the-art crystalline electrocatalysts comprising nonprecious metals. Long-term durability tests show that Ni(PO) maintains its OER activity even after 1000 repeated potential cycles while retaining its elemental composition and Raman spectrum. To understand the excellent OER activities of Ni-based phosphates, the atomic configurations within their crystals are examined. Remarkably, a clear correlation between Ni-O bond length and OER overpotentials is observed in both Ni-based phosphates and NiO, , shorter Ni-O bond lengths are highly beneficial for the OER. Density functional theory (DFT) calculations revealed that the outstanding OER activities of Ni-based phosphates are facilitated by their favorable electronic orbitals, which strengthen the Ni-O bond and improve the adsorption of OER intermediates on Ni sites. This mechanism is substantiated by DFT calculations employing surface slab models, where the adsorption of OER intermediates on the surface of Ni-based phosphates is more energetically favorable than on the surface of NiO. Hence, Ni-based phosphates are promising OER electrocatalysts, and this study provides important guidelines to further improve Ni-based electrocatalysts.
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http://dx.doi.org/10.1039/d4na00794h | DOI Listing |
Nanoscale Adv
December 2024
Laboratory for Chemistry and Life Science, Institute of Integrated Research, Institute of Science Tokyo Yokohama Kanagawa 226-8501 Japan
Metal phosphate-type compounds have been utilized in diverse applications, and their distinctive chemical properties have recently opened avenues for their use as catalysts. Metal phosphates have previously demonstrated significant electrocatalytic activity for the anodic oxygen evolution reaction (OER) in electrochemical water splitting. However, the critical factors influencing OER electrocatalysis on Ni-based phosphates have been insufficiently explored.
View Article and Find Full Text PDFACS Appl Mater Interfaces
October 2023
School of Urban and Environmental Sciences, Peking University, Beijing 100871, China.
CO hydrogenation via the reverse water gas shift (RWGS) reaction is a promising strategy for CO utilization while constructing Ni-based catalysts with high catalytic activity and perfect CO selectivity remains a great challenging. Here, we demonstrate that the product selectivity for CO hydrogenation can be significantly tuned from CH to CO by phosphating of SiO-supported Ni catalysts due to the geometric effect. Interestingly, nickel phosphide catalysts with different crystalline phases (NiP and NiP) differ sharply in CO conversion, and NiP is remarkably more active.
View Article and Find Full Text PDFTalanta
September 2022
School of Chemistry and Environmental Engineering, Sichuan University of Science and Engineering, Zigong, 643000, China.
In this work, spherical Ni-based metal-organic frameworks (Ni-MOFs) were used as precursors for preparing nanorod-like nickel phosphate (r-NiPO) with enhanced electro-catalytic properties in detection of glucose. It was found that the addition of nickel ion has a profound effect on construction of nickel phosphate with flower-like, rod-like, and ribbon-like structure in presence of HPO. The r-NiPO consisted of multiple phases of nickel phosphate showed porous, interconnected structure and abundant active Ni(II)/Ni(III) pairs, which was beneficial to facilitate glucose oxidation.
View Article and Find Full Text PDFNat Commun
May 2022
The State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, 200050, China.
Langmuir
February 2022
School of Chemistry and Chemical Engineering, Ningxia Key Laboratory of Solar Chemical Conversion Technology, Key Laboratory for Chemical Engineering and Technology, State Ethnic Affairs Commission, North Minzu University, Yinchuan 750021, P. R. China.
Here, an S-scheme heterojunction was constructed on the basis of the modification of a Ni-based metal-organic framework (Ni-MOF) by different in situ treatment strategies. First, NiS, NiO, and NiP were derived in situ on the surface of Ni-MOF through surface sulfonation, oxidation, and phosphatizing treatments. They can efficiently accept the electrons from the conduction band of Ni-MOF as the trap centers, thus improving the hydrogen production activity.
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