2019
DOI: 10.1016/s1872-2067(19)63363-2
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P-doped mesoporous carbons for high-efficiency electrocatalytic oxygen reduction

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Cited by 41 publications
(19 citation statements)
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References 39 publications
(34 reference statements)
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“…Therefore, after NaBH 4 treatment, the spectra centers of the obtained PNC−B and PNC−B/E are obviously shifted to lower binding energy for decreasing ∼0.4 eV compared to PNC and PNC−E (seen the inset of Figure 3a). Commonly, the binding energy of P−C, P−N and P−O bonds are at 132.7 eV, 133.4 eV and 135.2 eV, respectively [15,26,40–42] . Accordingly, the P 2p spectra of PNC and PNC−E were fitted, as shown in Figure 3a.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Therefore, after NaBH 4 treatment, the spectra centers of the obtained PNC−B and PNC−B/E are obviously shifted to lower binding energy for decreasing ∼0.4 eV compared to PNC and PNC−E (seen the inset of Figure 3a). Commonly, the binding energy of P−C, P−N and P−O bonds are at 132.7 eV, 133.4 eV and 135.2 eV, respectively [15,26,40–42] . Accordingly, the P 2p spectra of PNC and PNC−E were fitted, as shown in Figure 3a.…”
Section: Resultsmentioning
confidence: 99%
“…Commonly, the binding energy of PÀ C, PÀ N and PÀ O bonds are at 132.7 eV, 133.4 eV and 135.2 eV, respectively. [15,26,[40][41][42] Accordingly, the P 2p spectra of PNC and PNCÀ E were fitted, as shown in Figure 3a. For PNC, the P element mainly exists in the form of PÀ N bonds.…”
Section: Resultsmentioning
confidence: 99%
“…While small-angle XRD patterns ( Figure 2B) of as-prepared electrocatalysts showed a mainly well-shaped peak at 2θ ≈ 1 , suggesting their ordered mesopore structure. [29][30][31] Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) are effective techniques to characterize the pore structure. The SEM pattern of highly ordered PMMA nanospheres prepared by emulsifier-free emulsion polymerization and horizontal deposition procedure was displayed in Figure 3A.…”
Section: Characterization Of the Catalystsmentioning
confidence: 99%
“…In principle, further modification of carbon materials through controlling the chemical composition and engineering desirable structure would energetically enhance electrocatalytic performance . On the one hand, the intentional introduction of non‐metal elements (N, F, P, S, etc ) into carbon materials can tailor their chemical and electronic properties, create the active sites and boost the O 2 adsorption, thus boosting the reduction reactions . Noticeably, recent researches have proved that doping two types of dopants into carbon materials can induce a synergistic effect based on the charge and spin density changes at the various sites of co‐doped materials, which would enhance reaction kinetics, exhibiting superior performance compared with single‐doped carbon catalysts .…”
Section: Introductionmentioning
confidence: 99%