Author:
Depijan M,Hantanasirisakul K,Pakawatpanurut P
Abstract
Abstract
The superior performance of the Ti3C2T
x
-based supercapacitor has recently gained much interest in the energy storage community. Nevertheless, its performance in most neutral electrolytes remains a challenge, plausibly due to unfavorable ion diffusion as a result of limited interlayer spacing within Ti3C2T
x
. Herein, protonated g-C3N4 (pg-C3N4) was composited into Ti3C2T
x
using layer-by-layer assembling process. The XRD measurement indicated the enlargement in the d-spacing after pg-C3N4 was introduced into Ti3C2T
x
. The elemental analysis found the presence of N atom within Ti3C2T
x
, which indicated successful incorporation of pg-C3N4. The cyclic voltammogram revealed the increase in potential window up to 1.1 V with an improved specific capacitance of 95 F g−1 at 2 mV s−1 for Ti3C2T
x
/pg-C3N4 in neutral MgSO4 electrolyte. Given the fact that Ti3C2T
x
-only electrode yielded the specific capacitance of only 77 F g−1, a better performance of the Ti3C2T
x
/pg-C3N4 composite could be attributed to better ion diffusion within the material. In fact, our analysis indicated that the composite showed higher degree of ion diffusion-dependent pseudocapacitive contribution when compared to Ti3C2T
x
.
Subject
Computer Science Applications,History,Education