Jia Henan, Cai Yifei, Lin Jinghuang, Liang Haoyan, Qi Junlei, Cao Jian, Feng Jicai, Fei WeiDong
State Key Laboratory of Advanced Welding and Joining Harbin Institute of Technology Harbin 150001 China.
Adv Sci (Weinh). 2018 Mar 6;5(5):1700887. doi: 10.1002/advs.201700887. eCollection 2018 May.
The potential window of aqueous supercapacitors is limited by the theoretical value (≈1.23 V) and is usually lower than ≈1 V, which hinders further improvements for energy density. Here, a simple and scalable method is developed to fabricate unique graphene quantum dot (GQD)/MnO heterostructural electrodes to extend the potential window to 0-1.3 V for high-performance aqueous supercapacitor. The GQD/MnO heterostructural electrode is fabricated by GQDs in situ formed on the surface of MnO nanosheet arrays with good interface bonding by the formation of Mn-O-C bonds. Further, it is interesting to find that the potential window can be extended to 1.3 V by a potential drop in the built-in electric field of the GQD/MnO heterostructural region. Additionally, the specific capacitance up to 1170 F g at a scan rate of 5 mV s (1094 F g at 0-1 V) and cycle performance (92.7%@10 000 cycles) between 0 and 1.3 V are observed. A 2.3 V aqueous GQD/MnO-3//nitrogen-doped graphene ASC is assembled, which exhibits the high energy density of 118 Wh kg at the power density of 923 W kg. This work opens new opportunities for developing high-voltage aqueous supercapacitors using in situ formed heterostructures to further increase energy density.
水系超级电容器的潜在窗口受理论值(≈1.23 V)限制,通常低于≈1 V,这阻碍了能量密度的进一步提升。在此,开发了一种简单且可扩展的方法来制备独特的石墨烯量子点(GQD)/MnO异质结构电极,以将高性能水系超级电容器的潜在窗口扩展至0 - 1.3 V。GQD/MnO异质结构电极是通过在MnO纳米片阵列表面原位形成GQDs,并通过形成Mn - O - C键实现良好的界面结合而制备的。此外,有趣的是发现通过GQD/MnO异质结构区域内建电场中的电位降,潜在窗口可扩展至1.3 V。此外,在5 mV s的扫描速率下观察到比电容高达1170 F g(在0 - 1 V时为1094 F g),以及在0至1.3 V之间的循环性能(10000次循环时为92.7%)。组装了一个2.3 V的水系GQD/MnO - 3//氮掺杂石墨烯不对称超级电容器,其在923 W kg的功率密度下展现出118 Wh kg的高能量密度。这项工作为利用原位形成的异质结构开发高压水系超级电容器以进一步提高能量密度开辟了新机遇。