Abstract
A polymerized luminol carbon nanotube (CNT) composite electrode was
developed via an in‐situ chemical polymerization (CpLum) process.
Density functional theory (DFT) simulation suggested the luminol
molecules were preferentially aligned flat on CNT. This was further
demonstrated by morphological study which showed the CpLum wrapped
around each CNT tube homogeneously with an average thickness of 4.5± 1.5
nm. The surface chemical analysis by X‐ray photoelectron spectroscopy
(XPS) revealed a progressive increase in the nitrogen content and
stabilized at 9%. Deconvolution of the high‐resolution N1s spectra
suggested the presence of secondary and tertiary amine functional groups
which are the signatures of polymerized luminol. The composite
electrodes exhibited a pseudocapacitive‐like behavior with 3.5 times
increase in charge storage. The contributions from the CpLum coating and
CNT substrate were differentiated and were further deconvoluted to
quantify the capacitive charge storage of each component. The thin CpLum
coating contributed 70% of the total charge storage through
pseudocapacitance. CpLum‐CNT electrodes also showed a high rate
capability and good cycling stability, very promising for
electrochemical capacitors.
| Original language | English |
|---|---|
| Journal | ChemElectroChem |
| Volume | 6 |
| Issue number | 21 |
| Pages (from-to) | 5454-5461 |
| Number of pages | 9 |
| ISSN | 2196-0216 |
| DOIs | |
| Publication status | Published - 2019 |
Keywords
- Polyluminol
- In situ oxidative polymerization
- Density functional calculations
- Electrochemical capacitors
- Charge contribution