Hefei National Laboratory for Physical Science at Microscale and Department of Chemistry, University of Science and Technology of China, Hefei, Anhui, 230026, P. R. China.
Adv Mater. 2017 Aug;29(29). doi: 10.1002/adma.201700214. Epub 2017 May 26.
Large-volume-expansion-induced material pulverization severely limits the electrochemical performance of red phosphorous (P) for energy-storage applications. Hollow nanospheres with porous shells are recognized as an ideal structure to resolve these issues. However, a chemical synthetic approach for preparing nanostructured red P is always of great challenge and hollow nanosphere structures of red P have not yet been fabricated. Herein, a wet solvothermal method to successfully fabricate hollow P nanospheres (HPNs) with porous shells via a gas-bubble-directed formation mechanism is developed. More importantly, due to the merits of the porous and hollow structures, these HPNs reveal the highest capacities (based on the weight of electrode materials) of 1285.7 mA h g for lithium-ion batteries and 1364.7 mA h g for sodium-ion batteries at 0.2 C, and excellent long-cycling performance.
大体积膨胀引起的材料粉碎严重限制了红磷(P)在储能应用中的电化学性能。具有多孔壳的空心纳米球被认为是解决这些问题的理想结构。然而,制备纳米结构红磷的化学合成方法一直具有很大的挑战性,并且尚未制备出红磷的空心纳米球结构。在此,通过气泡导向形成机制,开发了一种湿溶胶-热法成功制备具有多孔壳的空心 P 纳米球(HPN)的方法。更重要的是,由于多孔和空心结构的优点,这些 HPN 在 0.2 C 时表现出最高的锂离子电池容量(基于电极材料的重量)为 1285.7 mA h g 和钠离子电池容量为 1364.7 mA h g,以及出色的长循环性能。