纳米复合材料
材料科学
循环伏安法
石墨氮化碳
化学工程
氢气储存
电极
电化学
拉曼光谱
多孔性
纳米技术
复合材料
化学
催化作用
有机化学
合金
物理化学
工程类
物理
光学
光催化
作者
Zahra Heydariyan,Rozita Monsef,Masoud Salavati‐Niasari
标识
DOI:10.1016/j.jallcom.2022.166564
摘要
The present work reports one-pot modified Pechini synthesis of porous Co3O4-CeO2 (CC) nanostructures with the templating environment of succinic acid, and further it is decorated with graphitic carbon nitride (g-C3N4 or CN) substrate. Interfacial architecture of the multicomponent nanocomposites can promote the synergistic effect by adjusting the weight percent of CC guest (30%, 50% and 70%) into CN host. The consequent changes in the compositional, morphological features and porosity of the resulting composites are unraveled by a combination of XRD, Raman, FE-SEM, HR-TEM, and BET analyses. Remarkably, the redox reactivity and considerable electronic conductivity of nanostructured electrode materials ascertains by cyclic voltammetry (CV) and chronopotentiometry charge–discharge (CCD) techniques in 2.0 M KOH medium. Fabricated Co3O4–CeO2/g-C3N4 (CC-CNx%) nanocomposites proved as the energetic electrode materials for realizing hydrogen storage performance at current of 1 mA. It is demonstrated that the CC/Cu platforms can produce the discharge efficiency of 619.25 mAhg−1 after 15 cycles. However, among the various adding, the ternary nanocomposites with 50.0 wt% CC nanoparticles achieved the higher discharge capacity of about 1020.53 mAhg−1 in three electrode cell. The coupling effect of interfacial architecture presented here suggests alternative insights into constructing uniformly nanocomposites for highly efficient energy storage applications.
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