2016
DOI: 10.1002/adma.201604080
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Hierarchical CoNi‐Sulfide Nanosheet Arrays Derived from Layered Double Hydroxides toward Efficient Hydrazine Electrooxidation

Abstract: A hierarchical CoNi-sulfide nanosheet array is fabricated via an in situ reduction of CoNi-layered double hydroxide (LDH) nanosheets, then a vulcanization process. The material inherits the morphology of the LDH precursor, consisting of well-distributed CoNi-alloy@CoNi-sulfide nanoparticles with a core-shell structure, and demonstrates promising performance toward hydrazine electrooxidation.

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Cited by 211 publications
(129 citation statements)
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“…Small molecule electrooxidation reaction (e.g., methanol, ethanol, hydrazine, formic acid, and glucose) is the heart process of direct liquid fuel cells, such as direct alcohol fuel cells, direct hydrazine hydrate fuel cells, and glucose biofuel cells, thus receiving tremendous attention 122–125. However, the efficient oxidation of small molecules is still impeded by the high overpotential.…”
Section: Electrocatalysis Application Of 2d Nanomaterialsmentioning
confidence: 99%
“…Small molecule electrooxidation reaction (e.g., methanol, ethanol, hydrazine, formic acid, and glucose) is the heart process of direct liquid fuel cells, such as direct alcohol fuel cells, direct hydrazine hydrate fuel cells, and glucose biofuel cells, thus receiving tremendous attention 122–125. However, the efficient oxidation of small molecules is still impeded by the high overpotential.…”
Section: Electrocatalysis Application Of 2d Nanomaterialsmentioning
confidence: 99%
“…[28][29][30] In addition, to properly make use of the intrinsic advantage of BSs, a novel fabrication approach is to directly grow the electrically conductive BSs on N-doped carbon materials (BSs@NMSs), which would ensure with a better contact with the conductive matrix. This will be in contrast to those processes completed at high hydrothermal temperatures [28,29,31,32] or chemical vapor deposition (CVD; they are usually higher than 600 °C), [33,34] which are tedious and time consuming. This will be in contrast to those processes completed at high hydrothermal temperatures [28,29,31,32] or chemical vapor deposition (CVD; they are usually higher than 600 °C), [33,34] which are tedious and time consuming.…”
Section: Introductionmentioning
confidence: 99%
“…X-ray photoelectron spectroscopy (XPS) was used to understand the reason for the OER activity enhancement observed with W 0.5 Co 0.5Àx Fe x trimetallic oxyhydroxides.F igure 5a shows the Co 2p spectra of various W 0.5 Co 0.5Àx Fe x oxyhydroxides.T he fitting analysis revealed the coexistence of Co 2+ and Co 3+ as the peaks at 798.1 and 782.4 eV correspond to Co 2+ 2p 1/2 and Co 2+ 2p 3/2 ,a nd the peaks at 796.6 and 780.7 eV belong to Co 3+ 2p 1/2 and Co 3+ 2p 3/2 , respectively,while the peaks located at 786.2 eV and 803.0 eV are satellite peaks. [5,48] As shown in Figure 5b,the Co 2+ /Co 3+ molar ratio increases with the addition of Fe,i ndicating electron transfer from Fe to Co,a nd Fe may inhibit the oxidation of Co. [49] However, for W 0.5 Co 0.3 Fe 0.2 ,the Co 2+ /Co 3+ molar ratio suddenly decreases,w hich is likely due to the formation of aseparate Fe phase for large Fe contents. [50] The volcano-like change in the Co 2+ /Co 3+ molar ratio as afunction of the amount of Fe is in good agreement with the trends in the OER activity (Figure 5c), suggesting that the on average lower Co oxidation state in W 0.5 Co 0.4 Fe 0.1 ,c aused by the addition of the right amount of Fe,o ptimizes the binding energy of surface oxygen intermediates and leads to improved kinetics,w hich is probably key for boosting the OER activity.…”
mentioning
confidence: 96%