Mohan Rao Tamtam, Rui Wang, Ravindranadh Koutavarapu, Gyu Sang Choi, Jaesool Shim, Nguyen To Hoai and Nam Nguyen Dang
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引用次数: 0
摘要
在这项工作中,利用三种不同的合成程序-分步(CC-1),单步(CC-2)和简单混合(CC-3)-来研究它们对双金属Cu/ co - mof异质结构形成的影响。所得到的MOF晶体结构显示Co与Cu金属离子的比例为1:1,并将其电化学活性与单个MOF的简单混合物进行了比较。为了最大限度地提高这些合成方法在超级电容器应用中的效益,进行了电化学分析。结果表明,CC-1在1 A g-1时的电容值为438 F -1,分别是CC-2和CC-3样品的1.14倍和2.76倍。这种显著的性能归功于每个2D材料组分的协同作用,以及最佳金属离子负载导致的稳定异质结构的形成。在非对称(AD)和对称(SD)硬币电池器件中进一步测试了性能最佳的CC-1电极。AD器件的能量密度(ED)为40.4 W h kg-1,功率密度(PD)为302.3 W kg-1,稳定性为75%;SD器件的ED为15.7 W h kg-1, PD为346.7 W kg-1,稳定性为88%。
A comparative study on the synthesis strategies and electrochemical features of bimetallic Cu/Co-MOFs†
In this work, three distinct synthetic procedures—step-by-step (CC-1), single-step (CC-2), and simple mixing (CC-3)—were utilized to investigate their effects on the formation of heterostructures in bimetallic Cu/Co-MOFs. The resulting MOF crystal structures revealed a 1 : 1 ratio of Co to Cu metal ions, and compared their electrochemical activities with a simple mixture of individual MOFs. To maximize the benefits of these synthesis approaches for supercapacitor uses, electrochemical analyses were conducted. Results revealed that the capacitance of CC-1 was 438 F g−1 at 1 A g−1, which was 1.14 times and 2.76 times higher than those of the CC-2 and CC-3 samples, respectively. This notable performance was attributed to the synergistic contributions from each 2D material component and the formation of a stable heterostructure that resulted from an optimal metal-ion loading. The best-performing CC-1 electrode was further tested in both asymmetric (AD) and symmetric (SD) coin cell devices. AD demonstrated an energy density (ED) of 40.4 W h kg−1 through a power density (PD) of 302.3 W kg−1 with 75% stability, while the SD device displayed an ED of 15.7 W h kg−1 and a PD of 346.7 W kg−1 with 88% stability.