Sulfur-Grafted Hollow Carbon Spheres for Potassium-Ion Battery Anodes.

Ding, Jia; Zhang, Hanlei; Zhou, Hui; Feng, Jun; Zheng, Xuerong; Zhong, Cheng; Paek, Eunsu; Hu, Wenbin et al. · Adv Mater · 2019

basic_science · Level V

Where this comes from

Abstract

Sulfur-rich carbons are minimally explored for potassium-ion batteries (KIBs). Here, a large amount of S (38 wt%) is chemically incorporated into a carbon host, creating sulfur-grafted hollow carbon spheres (SHCS) for KIB anodes. The SHCS architecture provides a combination of nanoscale (≈40 nm) diffusion distances and CS chemical bonding to minimize cycling capacity decay and Coulombic efficiency (CE) loss. The SHCS exhibit a reversible capacity of 581 mAh g<sup>-1</sup> (at 0.025 A g<sup>-1</sup> ), which is the highest reversible capacity reported for any carbon-based KIB anode. Electrochemical analysis of S-free carbon spheres baseline demonstrates that both the carbon matrix and the sulfur species are highly electrochemically active. SHCS also show excellent rate capability, achieving 202, 160, and 110 mAh g<sup>-1</sup> at 1.5, 3, and 5 A g<sup>-1</sup> , respectively. The electrode maintains 93% of the capacity from the 5th to 1000th cycle at 3 A g<sup>-1</sup> , with steady-state CE being near 100%. Raman analysis indicates reversible breakage of CS and SS bonds upon potassiation to 0.01 V versus K/K<sup>+</sup> . The galvanostatic intermittent titration technique (GITT) analysis provides voltage-dependent K<sup>+</sup> diffusion coefficients that range from 10<sup>-10</sup> to 10<sup>-12</sup> cm<sup>2</sup> s<sup>-1</sup> upon potassiation and depotassiation, with approximately five times higher coefficient for the former.