2021
DOI: 10.1039/d1na00304f
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Boron vacancy: a strategy to boost the oxygen reduction reaction of hexagonal boron nitride nanosheet in hBN–MoS2 heterostructure

Abstract: Incorporation of vacancies in a system considered as proficient defect engineering in general catalytic modulation. Among the two-dimensional materials, surface active sites’ deficiency and high band gap restrict hexagonal boron...

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Cited by 20 publications
(12 citation statements)
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“…The electronic structure of BN indicates the presence of boron vacancies on the basal plane that provide excellent charge transport pathways . Two peaks in the deconvoluted N 1s spectrum in Figure g were associated with N–B (398.8 eV) and N–H (∼400.5 eV).…”
Section: Resultsmentioning
confidence: 99%
“…The electronic structure of BN indicates the presence of boron vacancies on the basal plane that provide excellent charge transport pathways . Two peaks in the deconvoluted N 1s spectrum in Figure g were associated with N–B (398.8 eV) and N–H (∼400.5 eV).…”
Section: Resultsmentioning
confidence: 99%
“…The possible reason is that VS 2 can increase the asymmetric spin density of sp 2 C in rGO and charge delocalization. Thus, the lower R ct and higher ECSA offer a higher density of accessible active sites on the hybrid catalyst, which enhances the synergistic effect between VS 2 and rGO for the superior ORR activity [55–57] . Tafel plots (Figure 5a) were also employed to assess their electrocatalytic activity.…”
Section: Resultsmentioning
confidence: 99%
“…Chronoamperometric analysis at a fixed potential of 0.65 V (Figure 6e) exhibits excellent durability of 98.1 % during 24 h for VS 2 /rGO with respect to the other two synthesized electrocatalysts and Pt/C (92.7 %, Figure S14). The improved LSV cycling stability and chronoamperometric durability of VS 2 /rGO electrode is attributed to the spin‐orbit coupling of V and S orbital states, forming strong synergistic interaction with rGO and making the electrocatalyst more stable and more active towards ORR [55] . The reason for the poor durability of Pt/C is likely due to agglomeration of Pt NPs on the amorphous surface of C support, which is highly corrosive in nature [50] .…”
Section: Resultsmentioning
confidence: 99%
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