2022
DOI: 10.1016/j.apsusc.2021.151367
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Engineering dual metal single-atom sites with the nitrogen-coordinated nonprecious catalyst for oxygen reduction reaction (ORR) in acidic electrolyte

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Cited by 38 publications
(14 citation statements)
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“…Raman spectroscopy can effectively characterize the disorderly and orderly crystal structures of carbon materials. It can be seen from the Figure 2D that there are two bands at 1350 and 1590 cm −1 , which matched with disordered carbon (D band) and graphitic carbon (G band), respectively ( He et al, 2020 ; Gharibi et al, 2022 ; Zhang et al, 2022 ). It can be concluded that the relative intensity ratios of the D and G band ( I D / I G ) of NC and Mn-N x /NC are 1.015 and 1.026, respectively, suggesting the formation of more defects in N-doped carbon after introduction of Mn, which helps enhance the electrocatalytic activity ( Rao et al, 2022d ; Zou et al, 2022 ).…”
Section: Resultsmentioning
confidence: 91%
“…Raman spectroscopy can effectively characterize the disorderly and orderly crystal structures of carbon materials. It can be seen from the Figure 2D that there are two bands at 1350 and 1590 cm −1 , which matched with disordered carbon (D band) and graphitic carbon (G band), respectively ( He et al, 2020 ; Gharibi et al, 2022 ; Zhang et al, 2022 ). It can be concluded that the relative intensity ratios of the D and G band ( I D / I G ) of NC and Mn-N x /NC are 1.015 and 1.026, respectively, suggesting the formation of more defects in N-doped carbon after introduction of Mn, which helps enhance the electrocatalytic activity ( Rao et al, 2022d ; Zou et al, 2022 ).…”
Section: Resultsmentioning
confidence: 91%
“…The steady-state linear sweep voltammetry (LSV) is utilized to evaluate the ORR activities of asobtained PCCNS catalysts (Figure 5a), the onset potential (E 0 ), and half-wave potential (E 1/2 ) of PCCNS and Pt/C catalysts are shown in Figure S9 (Supporting Information). The PCCNS-20 present relatively higher E 0 (0.87 V vs RHE) and E 1/2 (0.77 V vs RHE) than others, with a marginal lower than commercial Pt/C, comparable to the decent Fe-N-C reports [23,[34][35][36][37] (Table 2).…”
Section: Resultsmentioning
confidence: 96%
“…The underlying mechanism can be summarized with the following points: (1) Fe and Zn atoms can be easily embedded into PPy@GO matrix to construct Fe-ZIF8@PPy@GO precursor. The Fe atoms can enhance the Fe-N x active center by either substituting the Zn atoms in ZIF-8 or inserting into PPy to cooperate with nitrogen Tafel slop [mV dec -1 ] Fe-N-C (S) catalyst [22] 0.83 0.71 -Co, Fe SAs/NC [33] 0.86 0.75 86 Fe-N-C/N-OMC [34] 0…”
Section: Resultsmentioning
confidence: 99%
“…Single-metal Fe PMS-AOPs Polysulfides adsorption-catalysis process ORR CO 2 RR [36,[42][43][44] Co OER Oxidation of 5-hydroxymethylfurfural [45,46] Dual-metal FeCo HER ORR PMS-AOPs [47][48][49] FeCu CO 2 RR PMS-AOPs [50,51] FeNi ORR OER Photocatalytic reaction CO 2 RR [52][53][54][55] FeMo PMS-AOPs [56] FeBi PMS-AOPs [57] CuNi CO 2 RR [58] ZnCo ORR [41] To prepare catalysts with a high density of active sites, a direct way is to increase the dosage of metal ions in the synthesis process. However, the high surface free energy of metal singleatom during high-temperature synthesis makes them apt to migrate and agglomerate to form NCs or NPs.…”
Section: Application Fieldsmentioning
confidence: 99%