Wang Qi, Zhong Tongtong, Wang Zhou
Key Laboratory of Liquid-Solid Structural Evolution and Processing of Materials of Ministry of Education, School of Materials Science and Engineering, Shandong University, Jinan 250061, China.
Nanomaterials (Basel). 2022 Aug 29;12(17):2984. doi: 10.3390/nano12172984.
Surface engineering has achieved great success in enhancing the electrochemical activity of CoO. However, the previously reported methods always involve high-temperature calcination processes which are prone to induce agglomeration of the nanostructure, leading to the attenuation of performance. In this work, CoO nanowires were successfully modified by a low-temperature NH/Ar plasma treatment, which simultaneously generated a porous structure and efficient nitrogen doping with no agglomeration. The modified N-CoO electrode exhibited remarkable performance due to the synergistic effect of the porous structure and nitrogen doping, which provided additional active sites for faradic transitions and improved charge transfer characteristics. The electrode achieved excellent supercapacitive performance with a maximum specific capacitance of 2862 mF/cm and superior cycling retention. Furthermore, the assembled asymmetric supercapacitor (N-CoO//AC) device exhibited an extended potential window of 1.5 V, a maximum specific energy of 80.5 Wh/kg, and a maximum specific power of 25.4 kW/kg with 91% capacity retention after 5000 charge-discharge cycles. Moreover, boosted hydrogen evolution reaction performance was also confirmed by the low overpotential (126 mV) and long-term stability. This work enlightens prospective research on the plasma-enhanced surface engineering strategies.
表面工程在提高CoO的电化学活性方面取得了巨大成功。然而,先前报道的方法总是涉及高温煅烧过程,这容易导致纳米结构的团聚,从而导致性能衰减。在这项工作中,通过低温NH/Ar等离子体处理成功地对CoO纳米线进行了改性,该处理同时产生了多孔结构并实现了有效的氮掺杂,且没有团聚现象。由于多孔结构和氮掺杂的协同效应,改性后的N-CoO电极表现出卓越的性能,这为法拉第跃迁提供了额外的活性位点并改善了电荷转移特性。该电极实现了优异的超级电容性能,最大比电容为2862 mF/cm²,且具有出色的循环保持率。此外,组装的不对称超级电容器(N-CoO//AC)器件展现出1.5 V的扩展电位窗口、80.5 Wh/kg的最大比能量以及25.4 kW/kg的最大比功率,在5000次充放电循环后容量保持率为91%。此外,低过电位(126 mV)和长期稳定性也证实了析氢反应性能得到了提升。这项工作为等离子体增强表面工程策略的前瞻性研究提供了启示。