超级电容器
材料科学
电极
色素敏化染料
钙钛矿(结构)
钴
辅助电极
能量转换效率
氧化还原
化学工程
电容
兴奋剂
纳米技术
分析化学(期刊)
光电子学
化学
冶金
物理化学
电解质
工程类
色谱法
作者
Chang Xu,Wenlu Yang,Jiaxin Zhao,Jingyuan Ma,Mingxing Wu
出处
期刊:ACS omega
[American Chemical Society]
日期:2021-09-17
卷期号:6 (38): 24931-24939
被引量:23
标识
DOI:10.1021/acsomega.1c03798
摘要
In the present study, three types of specific solid, core–shell, and hollow structured cobalt and iron co-doped MoS2 nanocubes (denoted as s-Co-Fe-MoSx, c-Co-Fe-MoSx, and h-Co-Fe-MoSx) are controllably synthesized for the first time by regulating the reactant mass ratios. The prepared Co-Fe-MoSx nanocubes can function as a counter electrode in dye-sensitized and perovskite solar cells (DSCs and PSCs) and a working electrode in a supercapacitor. In the DSC system, the c-Co-Fe-MoSx nanocubes exhibit the maximum catalytic activity to the Co3+/2+ redox couple regeneration, and the device achieves a power conversion efficiency (PCE) of 8.69%, significantly higher than the devices using s-Co-Fe-MoSx (6.61%) and h-Co-Fe-MoSx (7.63%) counter electrodes. Similarly, all of the prepared Co-Fe-MoSx nanocubes show decent activity in PSCs and the device using the c-Co-Fe-MoSx counter electrode achieves the highest PCE of 6.88%. It is worth noting that, as the supercapacitor working electrode, the h-Co-Fe-MoSx exhibits a specific capacitance of 85.4 F g–1, significantly higher than the parallel values achieved by the s-Co-Fe-MoSx and c-Co-Fe-MoSx electrodes under identical conditions.
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