Details

Autor(en) / Beteiligte

• He, Jiarui
• Chen, Yuanfu
• Lv, Weiqiang
• Wen, Kechun
• Xu, Chen
• Zhang, Wanli
• Li, Yanrong
• Qin, Wu
• He, Weidong

Titel

From Metal–Organic Framework to Li2S@C–Co–N Nanoporous Architecture: A High-Capacity Cathode for Lithium–Sulfur Batteries

Ist Teil von

• ACS nano, 2016-12, Vol.10 (12), p.10981-10987

Ort / Verlag

American Chemical Society

Erscheinungsjahr

2016

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• Owing to the high theoretical specific capacity (1166 mAh g–1), lithium sulfide (Li2S) has been considered as a promising cathode material for Li–S batteries. However, the polysulfide dissolution and low electronic conductivity of Li2S limit its further application in next-generation Li–S batteries. In this report, a nanoporous Li2S@C–Co–N cathode is synthesized by liquid infiltration–evaporation of ultrafine Li2S nanoparticles into graphitic carbon co-doped with cobalt and nitrogen (C–Co–N) derived from metal–organic frameworks. The obtained Li2S@C–Co–N architecture remarkably immobilizes Li2S within the cathode structure through physical and chemical molecular interactions. Owing to the synergistic interactions between C–Co–N and Li2S nanoparticles, the Li2S@C–Co–N composite delivers a reversible capacity of 1155.3 (99.1% of theoretical value) at the initial cycle and 929.6 mAh g–1 after 300 cycles, with nearly 100% Coulombic efficiency and a capacity fading of 0.06% per cycle. It exhibits excellent rate capacities of 950.6, 898.8, and 604.1 mAh g–1 at 1C, 2C, and 4C, respectively. Such a cathode structure is promising for practical applications in high-performance Li–S batteries.