Cui Lifeng, Wang Zhide, Kang Shifei, Fang Yanyan, Chen Ya, Gao Weikang, Zhang Zhiyuan, Gao Xin, Song Chunyu, Chen Xiaodong, Wang Yangang, Wang Guoxiu
College of Smart Energy, Shanghai Jiao Tong University, Shanghai 200240, PR China.
Southern Marine Science and Engineering Guangdong Laboratory (Zhanjiang), Zhanjiang 524000, PR China.
ACS Appl Mater Interfaces. 2022 Mar 16;14(10):12551-12561. doi: 10.1021/acsami.1c24989. Epub 2022 Mar 8.
Potassium-ion batteries (KIBs) are gradually being considered as an alternative for lithium-ion batteries because of their non-negligible advantages such as abundance and low expenditure of K, as well as higher electrochemical potential than another alternative─sodium-ion batteries. Nevertheless, when the electrode materials are inserted and extracted with large-sized K ions, the tremendous volume change will cause the collapse of the microstructures of electrodes and make the charging/discharging process irreversible, thus disapproving their extended application. In response to this, we put forward a feasible strategy to realize the in situ assembly of layered MoSe nanosheets onto N, P codoped hollow carbon nanospheres (MoSe/NP-HCNSs) through thermal annealing and heteroatom doping strategies, and the resulting nanoengineered material can function well as an anode for KIBs. This cleverly designed nanostructure of MoSe/NP-HCNS can broaden the interlayer spacing of MoSe to boost the efficiency of the insertion/extraction of K ions and also can accommodate large volume change-caused mechanical strain, facilitate electrolyte penetration, and prevent the aggregation of MoSe nanosheets. This synthetic method generates abundant defects to increase the amounts of active sites, as well as conductivity. The hierarchical nanostructure can effectively increase the proportion of pseudo-capacitance and promote interfacial electronic transfer and K diffusion, thus imparting great electrochemical performance. The MoSe/NP-HCNS anode exhibits a high reversible capacity of 239.9 mA h g at 0.1 A g after 200 cycles and an ultralong cycling life of 161.1 mA h g at 1 A g for a long period of 1000 cycles. This nanoengineering method opens up new insights into the development of promising anode materials for KIBs.
钾离子电池(KIBs)因其具有不可忽视的优势,如钾资源丰富、成本低,且电化学势高于另一种替代方案——钠离子电池,正逐渐被视为锂离子电池的替代品。然而,当电极材料插入和脱出大尺寸钾离子时,巨大的体积变化会导致电极微观结构坍塌,使充放电过程不可逆,从而不利于其广泛应用。针对这一问题,我们提出了一种可行的策略,通过热退火和杂原子掺杂策略,实现层状MoSe纳米片在氮、磷共掺杂空心碳纳米球(MoSe/NP-HCNSs)上的原位组装,所得的纳米工程材料可作为KIBs的阳极发挥良好作用。MoSe/NP-HCNS这种巧妙设计的纳米结构可以拓宽MoSe的层间距,提高钾离子插入/脱出效率,还能适应大体积变化引起的机械应变,促进电解质渗透,并防止MoSe纳米片聚集。这种合成方法产生大量缺陷,增加了活性位点数量以及导电性。分级纳米结构可有效提高赝电容比例,促进界面电子转移和钾扩散,从而赋予其优异的电化学性能。MoSe/NP-HCNS阳极在0.1 A g下循环200次后,可逆容量高达239.9 mA h g,在1 A g下经过1000次长循环后,超长循环寿命可达161.1 mA h g。这种纳米工程方法为开发有前景的KIBs阳极材料开辟了新的思路。