甲基橙
光催化
高分辨率透射电子显微镜
材料科学
异质结
光致发光
可见光谱
透射电子显微镜
扫描电子显微镜
光化学
电子顺磁共振
漫反射红外傅里叶变换
光谱学
载流子
光电子学
纳米技术
化学
催化作用
核磁共振
有机化学
复合材料
物理
量子力学
作者
Changcun Han,Lei Ge,Changfeng Chen,Yujing Li,Xinlai Xiao,Yuanna Zhang,Lele Guo
标识
DOI:10.1016/j.apcatb.2013.09.038
摘要
Novel visible-light-induced Co3O4-g-C3N4 heterojunction photocatalysts were synthesized via a facile mixing-and-heating method. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), ultraviolet–visible diffuse reflection spectroscopy (DRS), electron spin resonance (ESR) and photoluminescence spectroscopy (PL). The heterojunction photocatalysts exhibit a significantly enhanced photocatalytic activity in degrading methyl orange (MO). The optimal Co3O4 content with the highest photocatalytic activity was determined to be 0.2 wt%. The synergetic effect between Co3O4 and g-C3N4 plays an important role in promoting photo-generated carrier separation. The ESR and PL results reveals that the enhanced photocatalytic activity of Co3O4-g-C3N4 was mainly due to the superior amount and longer lifetime of oxidative radicals (O2−), as well as the efficient separation of charge carriers. Possible mechanism is proposed for the high photocatalytic activity of heterojunction structures, to guide the design of photocatalysts.
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