2018
DOI: 10.1016/j.apsusc.2017.12.124
|View full text |Cite
|
Sign up to set email alerts
|

Nitrogen and sulphur co-doped multiwalled carbon nanotubes as an efficient electrocatalyst for improved oxygen electroreduction

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
24
0

Year Published

2018
2018
2022
2022

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 31 publications
(24 citation statements)
references
References 31 publications
0
24
0
Order By: Relevance
“…The high‐resolved C1s XPS spectrum (Figure 2C) can be deconvoluted into 5 peaks at 284.3 (28.69%), 284.8 (21.26%), 286.0 (19.29%), 287.4 (12.65%), and 288.0 eV (18.11%), which are attributed to CC, CC, CN/CS, CO, and CO bonds, respectively . The spectrum of O1s (Figure 2D) is divided into 3 peaks at 531.0 (61.76%), 531.7 (31.14%), and 535.0 eV (7.10%) that can be assigned to CO, OH, and OCO groups . In the deconvoluted N1s spectrum (Figure 2E), binding energies located at 397.6 (32.14%), 399.4(63.56%), and 401.2 eV (4.3%) are assigned to pyridinic N, pyrrolic N, and graphitic‐N, respectively .…”
Section: Resultsmentioning
confidence: 99%
“…The high‐resolved C1s XPS spectrum (Figure 2C) can be deconvoluted into 5 peaks at 284.3 (28.69%), 284.8 (21.26%), 286.0 (19.29%), 287.4 (12.65%), and 288.0 eV (18.11%), which are attributed to CC, CC, CN/CS, CO, and CO bonds, respectively . The spectrum of O1s (Figure 2D) is divided into 3 peaks at 531.0 (61.76%), 531.7 (31.14%), and 535.0 eV (7.10%) that can be assigned to CO, OH, and OCO groups . In the deconvoluted N1s spectrum (Figure 2E), binding energies located at 397.6 (32.14%), 399.4(63.56%), and 401.2 eV (4.3%) are assigned to pyridinic N, pyrrolic N, and graphitic‐N, respectively .…”
Section: Resultsmentioning
confidence: 99%
“…The electrochemical studies confirmed that upon optimization of the NSCD/C catalyst, the ORR kinetics could be drastically improved with Eonset of 0.87 V vs RHE and JL of 5.0 mA cm −2 in alkaline condition. Additionally, the catalyst shows a single step, nearly 4-electron transfer pathway, indicating first order kinetics similar to that of Pt/C based catalysts [92]. Moreover, the incorporation of N and S into defects of CNTs generated by different ball milling periods was investigated.…”
Section: Doped Cnts For Fuel Cellsmentioning
confidence: 87%
“…The stability of the catalyst should be tested either in the form of their retention of activity after many cycles (upward of 10 000) or prolonged voltage holds (>1 00 00 s). Although tolerance to MeOH is often a metric that is used to assess the quality of metal‐free catalysts, it has become abundantly clear that heteroatom‐doped catalysts are not active for MeOH oxidation, and so do not suffer voltage loss due to MeOH crossover, exemplified by the majority of recent examples in the literature . It is apparent that this is now a largely meaningless metric for metal‐free catalysts, and all non‐PGM (Pt group metal) materials should be assumed to have good tolerance to MeOH cross‐over.…”
Section: Best Practice For Oxygen and Hydrogen Electrocatalysismentioning
confidence: 99%