Green preparation of nitrogen vacancies enriched g-C3N4 for efficient photocatalytic reduction of CO2 and Cr(VI)

IF 9.4 1区 化学 Q1 CHEMISTRY, PHYSICAL Journal of Colloid and Interface Science Pub Date : 2024-12-01 DOI:10.1016/j.jcis.2024.11.237
Yuyang Gong, Jiufu Chen, Dongmei Ma, Junbo Zhong
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Abstract

Introducing vacancies has emerged as one of the valid strategies to modulate the photocatalytic performance of graphitic carbon nitride (g-C3N4). Introduction of nitrogen vacancies into g-C3N4 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 (CO2). In this study, a series of g-C3N4 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 CO2 and Cr(VI) reduction. On the 11CN photocatalyst (0.5 g g-C3N4 was treated by 11 g sodium bisulfite), the generation rate of CO and CH4 is 5.74 μmol·g−1·h−1 and 1.30 μmol·g−1·h−1, respectively, which is 3.19 times and 8.29 times higher than those on the reference g-C3N4 (CO: 1.37 μmol·g−1·h−1, CH4: 0.14 μmol·g−1·h−1). Under irradiation by three distinct monochromatic lights, the apparent quantum yield (AQY) of 11CN is also superior to that of the reference g-C3N4. 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-C3N4. Stability of the catalyst was verified through cycling experiments, and the samples exhibit promising practical application prospect. The mechanism of photocatalytic CO2 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-C3N4-based photocatalytic materials, providing an effective approach to enhance the photocatalytic activity of g-C3N4 in photocatalytic CO2 and Cr(VI) reduction.

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绿色制备富氮空位g-C3N4高效光催化还原CO2和Cr(VI)。
引入空位已成为调控石墨氮化碳(g-C3N4)光催化性能的有效策略之一。在g-C3N4中引入氮空位可以产生缺陷能级并捕获电子,从而加速e-/h+对的分离,有效地提高光催化活性。氮空位也可以作为吸附活性位点,增强催化剂对目标分子(CO2)的吸附能力。本研究以亚硫酸氢钠为原料,采用绿色简便的方法制备了一系列氮空位丰富的g-C3N4。氮空位的成功引入赋予了光催化剂更多的活性位点,优化了能带结构,显著促进了光激发载流子的分离,从而显著增强了光催化CO2和Cr(VI)的还原。在11CN光催化剂上(0.5 g g- c3n4用11g亚硫酸氢钠处理),CO和CH4的生成速率分别为5.74 μmol·g-1·h-1和1.30 μmol·g-1·h-1,是对照g- c3n4 (CO: 1.37 μmol·g-1·h-1, CH4: 0.14 μmol·g-1·h-1)的3.19倍和8.29倍。在三种不同单色光的照射下,11CN的表观量子产率(AQY)也优于参考物g-C3N4。结果表明,11CN对Cr(VI)的光催化还原速率常数比参考g-C3N4高1.79倍。通过循环实验验证了催化剂的稳定性,样品具有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)分析了光催化CO2还原的机理和中间产物的转化途径。本研究提出了在g-C3N4基光催化材料中引入氮空位的新策略,为提高g-C3N4光催化还原CO2和Cr(VI)的光催化活性提供了有效途径。
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来源期刊
CiteScore
16.10
自引率
7.10%
发文量
2568
审稿时长
2 months
期刊介绍: The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality. Emphasis: The journal emphasizes fundamental scientific innovation within the following categories: A.Colloidal Materials and Nanomaterials B.Soft Colloidal and Self-Assembly Systems C.Adsorption, Catalysis, and Electrochemistry D.Interfacial Processes, Capillarity, and Wetting E.Biomaterials and Nanomedicine F.Energy Conversion and Storage, and Environmental Technologies
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