Construction of High-Activity Nano-NiTiO3/g-C3N4 Composite Catalysts for Enhanced Photodegradation Activities under Visible Light

Da Li, Zhan Yang, Kun Wang, Lan Zhang, Linglong Shi, Abdul Qadeer, Jiao Dong, Haoyu Ren
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Abstract

Nickel titanate (NiTiO3) semiconductors and graphitic carbon nitride (g-C3N4) have attracted great attention as photocatalysts in the degradation of environmental pollutants because of their visible-light-driven activity. But the utilizations of both semiconductors are limited by their low specific surface area. In this study, a nano-NiTiO3/g-C3N4 photocatalyst was successfully synthesized by optimizing the preparation method of photocatalyst precursors. Compared with the bulk g-C3N4 and bulk NiTiO3/g-C3N4 composite photocatalysts, the nano-NiTiO3/g-C3N4 composite catalyst displayed a larger specific surface area, a more abundant pore size structure, and superior carrier separation capabilities. According to the pseudo-first-order, the degradation rate of MB was more than 2.5–19.7 times higher than that of previous studies. The superoxide radicals (·O2−) and holes (h+) played significant roles in the photocatalytic reaction of MB. This study provides a new idea for the synthesis of photocatalysts and the improvement in photocatalytic performance.
构建高活性纳米镍钛氧化物/克-C3N4 复合催化剂以增强可见光下的光降解活性
钛酸镍(NiTiO3)半导体和氮化石墨碳(g-C3N4)因其在可见光驱动下的活性,在作为光催化剂降解环境污染物方面引起了极大关注。但是,由于这两种半导体的比表面积较低,其利用受到限制。本研究通过优化光催化剂前驱体的制备方法,成功合成了纳米 NiTiO3/g-C3N4 光催化剂。与块状 g-C3N4 和块状 NiTiO3/g-C3N4 复合光催化剂相比,纳米 NiTiO3/g-C3N4 复合催化剂比表面积更大,孔径结构更丰富,载流子分离能力更强。根据伪一阶法,甲基溴的降解率是之前研究的 2.5-19.7 倍。超氧自由基(-O2-)和空穴(h+)在甲基溴的光催化反应中发挥了重要作用。这项研究为光催化剂的合成和光催化性能的提高提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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