2016
DOI: 10.1039/c6ra21958f
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Nitrogen- and sulfur-doped carbon nanoplatelets via thermal annealing of alkaline lignin with urea as efficient electrocatalysts for oxygen reduction reaction

Abstract: Novel N–S–C hybrids were synthesized by a facile one-step pyrolysis method, in which the obtained N–S–C 900 was a robust catalyst with enhanced ORR activity and excellent operational stability in alkaline media, superior to the Pt/C catalyst.

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Cited by 32 publications
(20 citation statements)
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“…The relative composition of N species is shown in Figure b. The pyridinic N and pyrrolic N contents are reduced whereas graphitic N content is gradually increased on rising of annealing temperature, indicating that pyridinic and pyrrolic N are less stable than graphitic N at higher temperature . The oxidized N content slightly increase from 6 to 6.9 % with temperature increase from 700 to 900 °C, but it decreases to 4.3 % at 1000 °C.…”
Section: Resultsmentioning
confidence: 99%
“…The relative composition of N species is shown in Figure b. The pyridinic N and pyrrolic N contents are reduced whereas graphitic N content is gradually increased on rising of annealing temperature, indicating that pyridinic and pyrrolic N are less stable than graphitic N at higher temperature . The oxidized N content slightly increase from 6 to 6.9 % with temperature increase from 700 to 900 °C, but it decreases to 4.3 % at 1000 °C.…”
Section: Resultsmentioning
confidence: 99%
“…A 3D N‐doped porous carbon with a large specific surface area (1012 m 2 g −1 ) also displayed high ORR catalytic activity and remarkable durability with a retention of 96.5% after 20 000 s . In addition, alkaline lignin‐derived N, S dual‐doped carbon nanoplatelets showed comparable ORR electrocatalytic activity, superior stability, and methanol tolerance to the commercial Pt/C catalyst in both alkaline and acidic electrolyte …”
Section: Applications Of Lignin‐derived Materials In Electrochemical mentioning
confidence: 99%
“…2c, the Co-CoO@C/C exhibits signicantly lower BET specic surface area than that of the Co-CoO@NC/NC-800. This might be due to the reason that the thermal decomposition of urea during the calcination would produce a large amount of gases, such as CO 2 , NH 3 , and other gaseous products, 46,47 which are helpful to the formation of the porous structure in the Co-CoO@NC/NC-800. Most interestingly, although the Co-CoO@NC/NC-700 and the Co-CoO@NC/NC-900 exhibit the N 2 adsorption/desorption isotherms comparable to those of the Co-CoO@NC/NC-800, their BET specic surface areas are much lower than that of the Co-CoO@NC/NC-800.…”
Section: Electrochemical Measurementmentioning
confidence: 99%