Abstract
One obstacle that hinders the development of rechargeable magnesium batteries (RMBs) is the limited selection of cathode materials with decent Mg diffusion kinetics due to the highly polarizing nature of divalent Mg2+. To promote Mg2+ diffusion kinetics, water molecules (H2O) are incorporated into the gaps of MoS2 with enlarged interlayer spacing through an electrochemically assisted method. Owing to the charge shielding effect of crystal H2O, the electrostatic interaction between Mg2+ and host frameworks is weakened, thus hydrous MoS2 (H−MoS2) delivers a Mg diffusion rate three times faster than that of MoS2 before hydration. The facilitated Mg diffusion kinetics in H−MoS2 ensure a high capacity of 190.3 mAh g−1 at 20 mA g−1, accompanied by excellent rate performance (75.1 mAh g−1 retains at 500 mA g−1). Additionally, crystal H2O plays the role of pillars, endowing that the layered structure of H−MoS2 retains stable during repetitive Mg intercalation, thus 91.2 % of initial capacity is retained after 300 cycles.
| Original language | English |
|---|---|
| Pages (from-to) | 4559-4563 |
| Number of pages | 5 |
| Journal | ChemElectroChem |
| Volume | 8 |
| Issue number | 23 |
| DOIs | |
| Publication status | Published - 1 Dec 2021 |
| Externally published | Yes |
Keywords
- Diffusion kinetics
- Molybdenum disulfide
- Shielding effect
- Water molecule
- charge shielding effect
- facilitated kinetics
- molybdenum disulfide
- rechargeable magnesium batteries
- structural HO
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