2021
DOI: 10.1016/s1872-2067(20)63730-5
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In situ evolution of surface Co2CrO4 to CoOOH/CrOOH by electrochemical method: Toward boosting electrocatalytic water oxidation

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Cited by 23 publications
(14 citation statements)
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“…Three O 1s peaks at 529.5, 530.9, and 532.3 eV were observed for Cr 2 Te 3 /CrOOH in Figure S4c, which correspond to the Cr−O, CrO−H, and H− O−H bonds. 37 Our results signify that the observed selfoptimization of OER performance should be related to the formation of Cr 2 Te 3 /CrOOH lateral heterostructures (Figure 2e). To understand the high OER activity of Cr 2 Te 3 /CrOOH heterostructure at atomic and electronic level, we resorted to first-principles calculation of the OER process based on the 4emechanism proposed by Nørskov et al on Cr 2 Te 3 , CrOOH, and Cr 2 Te 3 /CrOOH heterostructure structure models.…”
supporting
confidence: 62%
See 1 more Smart Citation
“…Three O 1s peaks at 529.5, 530.9, and 532.3 eV were observed for Cr 2 Te 3 /CrOOH in Figure S4c, which correspond to the Cr−O, CrO−H, and H− O−H bonds. 37 Our results signify that the observed selfoptimization of OER performance should be related to the formation of Cr 2 Te 3 /CrOOH lateral heterostructures (Figure 2e). To understand the high OER activity of Cr 2 Te 3 /CrOOH heterostructure at atomic and electronic level, we resorted to first-principles calculation of the OER process based on the 4emechanism proposed by Nørskov et al on Cr 2 Te 3 , CrOOH, and Cr 2 Te 3 /CrOOH heterostructure structure models.…”
supporting
confidence: 62%
“…In the Te 3d region, the doublet peaks for Te 2– 3d 5/2 and Te 2– 3d 3/2 appear at 572.6 and 582.8 eV, respectively. Three O 1s peaks at 529.5, 530.9, and 532.3 eV were observed for Cr 2 Te 3 /CrOOH in Figure S4c, which correspond to the Cr–O, CrO–H, and H–O–H bonds . Our results signify that the observed self-optimization of OER performance should be related to the formation of Cr 2 Te 3 /CrOOH lateral heterostructures (Figure e).…”
supporting
confidence: 54%
“…Meanwhile, a lower R ct was observed for Co 2 PÀ CuP 2 /NF than all other control samples, demonstrating a lower resistance at the electrode-electrolyte interface, which results in rapid electron transfer kinetics (Figure 4e). [33] The exchange current density (j 0 ) is calculated according to the Tafel slope to evaluate the intrinsic activity of the catalyst. The j 0 of Co 2 PÀ CuP 2 /NF (0.80 mA cm À 2 ) was significantly higher than Co 2 P/NF (0.75 mA cm À 2 ) and CuP 2 /NF (0.25 mA cm À 2 ), verifying that it has good intrinsic HER activity (Figure 4f).…”
Section: Electrocatalytic Performancementioning
confidence: 99%
“…As a half-reaction of water-splitting, the cathodic HER efficiency acts as a key role in reducing the energy consumption during hydrogen generation. Thus, it is of importance to develop electrocatalysts with advantageous catalytic performance for HERs [ 15 , 16 , 17 , 18 , 19 , 20 , 21 ]. At present, Pt-based nanomaterials are still the state-of-the-art electrocatalysts for HERs due to having the lowest overpotential and the smallest Tafel slope [ 22 , 23 , 24 ].…”
Section: Introductionmentioning
confidence: 99%