Multi-function hollow nanorod as an efficient sulfur host accelerates sulfur redox reactions for high-performance Li-S batteries

The "shuttle effect" of lithium polysulfides (LiPSs) leads to loss of active materials and the deterioration of cycle stability, which seriously restricts the practical progress of lithium-sulfur (Li-S) batteries. The diffusion of soluble discharge intermediate is the root cause of the above problems. Herein, we synthesized a porous organic framework material (HUT-8) based on triazine network, the polar groups above the hollow structure can not only adsorb LiPSs through electron donating effect, but also anchored cobalt (II) ions provide a large number of binding sites for the in-situ growth of CoS2. This ensured maximized exposure of catalytic centre and improve their interactions with sulfur redox species under the confinement of mesopores, which can catalytically accelerate capture/diffusion of LiPSs and precipitation/decomposition of Li2S. Based on the synergistic effect of the composite materials, the CoS2-HUT-8/S cathode maintained a capacity of 583 mAh g(-1) after 500 cycles at 1 C, and a minimum capacity fading rate of 0.046% per cycle. A freestanding CoS2-HUT-8/S cathode with sulfur loading of 5.2 mg cm(-2) delivered a high areal capacity of 4.01 mAh cm(-2) under a lean electrolyte, which would provide great potential for the practical progress of Li-S batteries. (C) 2022 Elsevier Inc. All rights reserved.