2018
DOI: 10.1039/c8cc01724g
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One-step synthesis of ultrathin α-Co(OH)2nanomeshes and their high electrocatalytic activity toward the oxygen evolution reaction

Abstract: Herein, we demonstrate for the first time the one-step synthesis of ultrathin α-Co(OH)2 nanomeshes by an imidazole-directed route. The α-Co(OH)2 nanomeshes combine the advantages of ultrathin thickness (3 nm), small mesopores (3.7 nm), large specific surface area (181.1 m2 g-1) and high surface oxygen vacancy density, which exhibit excellent electrocatalytic performance for the oxygen evolution reaction.

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Cited by 73 publications
(52 citation statements)
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“…[8] For example, the large interlayer spacing and nanosheet (NS) structure of Co(OH) 2 are conducive to facilitate ion transport and provide large active area, respectively, which is vital to accelerate the OER kinetics in alkaline electrolytes. [9] However, Co(OH) 2 NS working as the anode catalyst of water electrolysis still cannot achieve ideal overpotential (lower than 300 mV at 10 mA cm À2 ), [10] indicating that the intrinsic activity of catalytic sites in Co(OH) 2 NS is limited. Consequently, it is critical to improve the catalytic efficiency and decrease the overpotential of Co(OH) 2 NS by engineering the surface atomic and electronic structures.…”
mentioning
confidence: 99%
“…[8] For example, the large interlayer spacing and nanosheet (NS) structure of Co(OH) 2 are conducive to facilitate ion transport and provide large active area, respectively, which is vital to accelerate the OER kinetics in alkaline electrolytes. [9] However, Co(OH) 2 NS working as the anode catalyst of water electrolysis still cannot achieve ideal overpotential (lower than 300 mV at 10 mA cm À2 ), [10] indicating that the intrinsic activity of catalytic sites in Co(OH) 2 NS is limited. Consequently, it is critical to improve the catalytic efficiency and decrease the overpotential of Co(OH) 2 NS by engineering the surface atomic and electronic structures.…”
mentioning
confidence: 99%
“…[8] For example, the large interlayer spacing and nanosheet (NS) structure of Co(OH) 2 are conducive to facilitate ion transport and provide large active area, respectively, which is vital to accelerate the OER kinetics in alkaline electrolytes. [9] However, Co(OH) 2 NS working as the anode catalyst of water electrolysis still cannot achieve ideal overpotential (lower than 300 mV at 10 mA cm À2 ), [10] indicating that the intrinsic activity of catalytic sites in Co(OH) 2 NS is limited. Consequently, it is critical to improve the catalytic efficiency and decrease the overpotential of Co(OH) 2 NS by engineering the surface atomic and electronic structures.Integrating metal nanoparticles with transition-metal compounds has been explored as a promising strategy to synthesize highly efficient electrocatalysts.…”
mentioning
confidence: 99%
“…However, by replacing water with water–methanol solution, homogeneous green dispersion can be obtained within 30 min, which presented the typical UV–vis absorption peaks of α-Co(OH) 2 at 586 and 642 nm (the inset of Figure 1a). 31 The characteristic X-ray diffraction (XRD) peaks of α-Co(OH) 2 at 9.6°, 19.3°, 33.4°, and 59.6° correspond to the lattice distances of (003), (006), (012), and (110) planes of α-Co(OH) 2 (JCPDS no. 46-0605) (Figure 1a).…”
Section: Results and Discussionmentioning
confidence: 99%
“…29,30 Ultrathin α-Co(OH) 2 nanostructures were prepared through 2-methylimidazole-mediated methods with good to excellent electrocatalytic activity. 3133 Transition-metal doping has also been proved as an efficient method to improve the electrocatalytic activity of Co(OH) 2 . 3437 Copper- or iron-doped Co(OH) 2 has been respectively reported to effectively catalyze water oxidation at the overpotential around 300 mV at 10 mA cm –2 current density with the former synthesized via NaBH 4 reducing method and the latter precipitated with NaOH in the presence of NaNO 3 , NH 4 F, and sodium citrate under N 2 atmosphere.…”
Section: Introductionmentioning
confidence: 99%