Highly conjugated graphitic 3D carbon frameworks for supercapacitors with long cycling stability
Highly conjugated graphitic 3D carbon frameworks for supercapacitors with long cycling stability
复制标题
用于具有长循环稳定性的超级电容器的高度共轭石墨3D碳框架
DOI:
10.1016/j.carbon.2016.08.081
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发表时间:
2016-11-01
期刊:
影响因子:
10.9
通讯作者:
Xin, John H.
中科院分区:
文献类型:
--
作者:
He, Liang;Zhang, Yabin;Xin, John H.
Bio-inspired by mussels' adhesion, a new protocol for the fabrication of large-sized carbon electrode materials (GCFs) is achieved through an adhesive self-assembly of in-situ-formed multilayered poly dopamine nanospheres along with a subsequent pyrolysis. The fabricated GCFs show a 3D hierarchical porous architecture consisting of highly graphitic carbon. These features allow a rapid diffusion, high loading and effective absorbing and exchanging of charged ions in GCF5, which endows GCFs superior electrochemical performance. When tested as supercapacitor electrodes, the GCFs exhibit a high volumetric capacitance of 105 F cm(-3) at a current density of 1.0 A cm(-3) within a potential window of 0-1.0 V in 0.5 M Na2SO4 solution. Meanwhile, the GCFs has been assembled a simple asymmetrical super capacitor, which can stably supply power to a LED and a small fan with an excellent cycling stability of 100% capacitance retention after 10000 charge/discharge cycles. Worthy to note, due to the versatile adhesive ability of polydopamine to almost all substrates, this developed protocol provides new avenues to fabricate large-sized core-shell electrodes, which is attractive in future portable devices. (C) 2016 Elsevier Ltd. All rights reserved.