2023
DOI: 10.1038/s41565-023-01407-1
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Ferromagnetic single-atom spin catalyst for boosting water splitting

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Cited by 131 publications
(53 citation statements)
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“…Additionally, increasing the remanent magnetism of the catalysts is also an effective method to boost the intrinsic activity without the assistance of magnetic field. Besides above oxides of magnetic element (Fe, Co, Ni), their hydroxides 115 and sulfides 116 the increase of magnetic field (0∼502 mT) (Figure 9H). The physics of magnetic-field enhancement on the OER is that the external magnetic field can align the magnetic domain configuration of multidomain FM catalysts in an orderly direction, as demonstrated by the schematic diagram in Figure 2C.…”
Section: Magnetic Field-enhanced Oermentioning
confidence: 94%
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“…Additionally, increasing the remanent magnetism of the catalysts is also an effective method to boost the intrinsic activity without the assistance of magnetic field. Besides above oxides of magnetic element (Fe, Co, Ni), their hydroxides 115 and sulfides 116 the increase of magnetic field (0∼502 mT) (Figure 9H). The physics of magnetic-field enhancement on the OER is that the external magnetic field can align the magnetic domain configuration of multidomain FM catalysts in an orderly direction, as demonstrated by the schematic diagram in Figure 2C.…”
Section: Magnetic Field-enhanced Oermentioning
confidence: 94%
“…Additionally, increasing the remanent magnetism of the catalysts is also an effective method to boost the intrinsic activity without the assistance of magnetic field. Besides above oxides of magnetic element (Fe, Co, Ni), their hydroxides and sulfides also exhibit obvious magnetic enhancement on OER activity (Figure G, H). For example, Ni, Co, Fe based layered double hydroxides (LDHs) (NCFL) have a strong spin magnetic effect about −34.8 mV/T (Figure G) and the OER performance of Ni doped MoSe 2 is gradually improved with the increase of magnetic field (0∼502 mT) (Figure H).…”
Section: Magnetism-enhanced Electrocatalysismentioning
confidence: 97%
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“…Transition metal doping is a common strategy for regulating electronic and geometric structures for enhanced intrinsic activities and exposed active sites. 8,9 Metal dopants with various electronegativities can transform the electronic structure of CoP. The differences in the radius of the dopants and the pristine atoms lead to lattice distortion and pore formation, improving the active sites and accelerating the mass transfer.…”
Section: Introductionmentioning
confidence: 99%
“…The oxygen evolution reaction (OER) is one of the key electrochemical reactions in energy conversion and storage, particularly in water-splitting and metal-air batteries. Due to its requirement for a four-electron proton-coupled transfer process, accompanied by the breaking of O–H bonds and formation of O–O bonds, the slow kinetics result in a relatively high overpotential to conquer the energy barriers. Hitherto, Ir- or Ru-based oxides and their composite materials have continued to be considered the most developed OER electrocatalysts despite their discontented durability, high cost, and scarcity. To address this issue, numerous attempts have been made to create highly efficient, cost-effective, and abundantly available OER catalysts. …”
Section: Introductionmentioning
confidence: 99%