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用于高效光催化还原 CO 和 Cr(VI) 的富含氮空位的 g-CN 的绿色制备

Green preparation of nitrogen vacancies enriched g-CN for efficient photocatalytic reduction of CO and Cr(VI).

作者信息

Gong Yuyang, Chen Jiufu, Ma Dongmei, Zhong Junbo

机构信息

Key Laboratory of Green Catalysis of Higher Education Institutes of Sichuan, College of Chemistry and Environmental Engineering, Sichuan University of Science and Engineering, Zigong 643000, PR China.

Key Laboratory of Green Catalysis of Higher Education Institutes of Sichuan, College of Chemistry and Environmental Engineering, Sichuan University of Science and Engineering, Zigong 643000, PR China.

出版信息

J Colloid Interface Sci. 2025 Mar 15;682:446-459. doi: 10.1016/j.jcis.2024.11.237. Epub 2024 Dec 1.

Abstract

Introducing vacancies has emerged as one of the valid strategies to modulate the photocatalytic performance of graphitic carbon nitride (g-CN). Introduction of nitrogen vacancies into g-CN can create defect energy levels and trap electrons, consequently accelerating the separation of e/h pairs and effectively boosting photocatalytic activity. Nitrogen vacancies can also serve as adsorption active sites, enhancing the adsorption capacity of the catalyst towards the target molecule (CO). In this study, a series of g-CN with abundant nitrogen vacancies were prepared using a green and facile strategy using sodium bisulfite treatment. Successful introduction of nitrogen vacancies endows with the photocatalyst more active sites, optimizes the band structure, significantly boosts the separation of photoexcited carriers, thereby remarkably enhancing photocatalytic CO and Cr(VI) reduction. On the 11CN photocatalyst (0.5 g g-CN was treated by 11 g sodium bisulfite), the generation rate of CO and CH is 5.74 μmol·g·h and 1.30 μmol·g·h, respectively, which is 3.19 times and 8.29 times higher than those on the reference g-CN (CO: 1.37 μmol·g·h, CH: 0.14 μmol·g·h). Under irradiation by three distinct monochromatic lights, the apparent quantum yield (AQY) of 11CN is also superior to that of the reference g-CN. Moreover, photocatalytic Cr(VI) reduction experiments were performed on the catalysts to demonstrate the universality of the catalysts The results show that the photocatalytic reduction rate constant of Cr(VI) by 11CN is 1.79 times higher than that over the reference g-CN. Stability of the catalyst was verified through cycling experiments, and the samples exhibit promising practical application prospect. The mechanism of photocatalytic CO reduction and the transformation pathway of intermediate products were elucidated using in-situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). This study introduces a new strategy of introducing nitrogen vacancies into g-CN-based photocatalytic materials, providing an effective approach to enhance the photocatalytic activity of g-CN in photocatalytic CO and Cr(VI) reduction.

摘要

引入空位已成为调节石墨相氮化碳(g-CN)光催化性能的有效策略之一。在g-CN中引入氮空位可产生缺陷能级并捕获电子,从而加速电子/空穴对的分离并有效提高光催化活性。氮空位还可作为吸附活性位点,增强催化剂对目标分子(CO)的吸附能力。在本研究中,采用亚硫酸氢钠处理的绿色简便策略制备了一系列具有丰富氮空位的g-CN。氮空位的成功引入赋予光催化剂更多活性位点,优化了能带结构,显著促进了光生载流子的分离,从而显著提高了光催化CO和Cr(VI)还原性能。在11CN光催化剂(0.5 g g-CN用11 g亚硫酸氢钠处理)上,CO和CH的生成速率分别为5.74 μmol·g·h和1.30 μmol·g·h,分别是参考g-CN(CO:1.37 μmol·g·h,CH:0.14 μmol·g·h)的3.19倍和8.29倍。在三种不同单色光照射下,11CN的表观量子产率(AQY)也优于参考g-CN。此外,对催化剂进行了光催化Cr(VI)还原实验以证明催化剂的通用性。结果表明,11CN对Cr(VI)的光催化还原速率常数比参考g-CN高1.79倍。通过循环实验验证了催化剂的稳定性,样品展现出良好的实际应用前景。利用原位漫反射红外傅里叶变换光谱(DRIFTS)阐明了光催化CO还原机理及中间产物的转化途径。本研究介绍了一种在g-CN基光催化材料中引入氮空位的新策略,为提高g-CN在光催化CO和Cr(VI)还原中的光催化活性提供了有效途径。

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