Wang Lifeng, Wang Haiyun, Zhang Shipeng, Ren Naiqing, Wu Ying, Wu Liang, Zhou Xuefeng, Yao Yu, Wu Xiaojun, Yu Yan
Hefei National Laboratory for Physical Sciences at the Microscale, Department of Materials Science and Engineering, CAS Key Laboratory of Materials for Energy Conversion, University of Science and Technology of China, Hefei, Anhui 230026, China.
State Key Laboratory of Photon-Technology in Western China Energy, International Collaborative Center on Photoelectric Technology and Nano Functional Materials, Institute of Photonics and Photon-Technology, Northwest University, Xi'an 710127, P.R. China.
ACS Nano. 2021 Sep 28;15(9):15218-15228. doi: 10.1021/acsnano.1c05778. Epub 2021 Aug 23.
The sluggish conversion kinetics and severe shuttle effect in room-temperature Na-S (RT Na-S) batteries cause knotty issues, such as poor rate performance, fast capacity decay as well as low Coulombic efficiency, which seriously impede their practical application. Therefore, exploiting cost-effective and efficient electrocatalysts for absorbing soluble long-chain sodium polysulfides (NaPSs) and expediting NaPSs conversion is of paramount importance. Herein, catalyst mining is first conducted by density functional theory calculations, which reveal that the alloying of Fe into Ni can tailor the electronic structure, leading to lower reaction energy barrier for polysulfide conversion. Based on this, FeNi@hollow porous carbon spheres (FeNi@HC) as a promising sulfur host for RT Na-S batteries are rationally designed and fabricated. As expected, the S@FeNi@HC cathode exhibits an excellent cycling stability (591 mAh g after 500 cycles at 2 A g) and outstanding rate performance (383 mAh g at 5 A g). Our work demonstrates an effective strategy (.., alloying strategy with a rich electron state) to design superior electrocatalysts for RT Na-S batteries.
室温钠硫(RT Na-S)电池中缓慢的转化动力学和严重的穿梭效应导致了棘手的问题,如倍率性能差、容量快速衰减以及库仑效率低等,这严重阻碍了它们的实际应用。因此,开发具有成本效益且高效的电催化剂以吸收可溶性长链多硫化钠(NaPSs)并加速NaPSs的转化至关重要。在此,首先通过密度泛函理论计算进行催化剂筛选,结果表明铁与镍合金化可以调整电子结构,从而降低多硫化物转化的反应能垒。基于此,合理设计并制备了FeNi@中空多孔碳球(FeNi@HC)作为RT Na-S电池颇具前景的硫载体。正如预期的那样,S@FeNi@HC正极表现出优异的循环稳定性(在2 A g下500次循环后为591 mAh g)和出色的倍率性能(在5 A g下为383 mAh g)。我们的工作展示了一种有效的策略(即具有丰富电子态的合金化策略)来设计用于RT Na-S电池的优质电催化剂。