Abstract
Na-ion batteries (NIBs) have attracted considerable attention in recent years owing to the high abundance and low cost of Na. It is well known that S doping can improve the electrochemical performance of carbon materials for NIBs. However, the current methods for S doping in carbons normally involve toxic precursors or rigorous conditions. In this work, we report a creative and facile strategy for preparing S-doped porous carbons (SCs) via the pyrolysis of conjugated microporous polymers (CMPs). Briefly, thiophene-based CMPs served as the precursors and doping sources simultaneously. Simple direct carbonization of CMPs produced S-doped carbon materials with highly porous structures. When used as an anode for NIBs, the SCs exhibited a high reversible capacity of 440 mAh g−1 at 50 mA g−1 after 100 cycles, superior rate capability, and excellent cycling stability (297 mAh g−1 after 1000 cycles at 500 mA g−1), outperforming most S-doped carbon materials reported thus far. The excellent performance of the SCs is attributed to the expanded lattice distance after S doping. Furthermore, we employed ex situ X-ray photoelectron spectroscopy to investigate the electrochemical reaction mechanism of the SCs during sodiation–desodiation, which can highlight the role of doped S for Na-ion storage.[Figure not available: see fulltext.].
| Original language | English |
|---|---|
| Article number | 60 |
| Journal | Nano-Micro Letters |
| Volume | 11 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1 Dec 2019 |
Keywords
- Conjugated microporous polymer
- Na-ion batteries
- Reaction mechanism
- S-doped porous carbons