Sodium ethoxide treatment induced enrichen nitrogen vacancies on g-C3N4 for efficient photocatalytic CO2 reduction and Cr(VI) removal

IF 4.3 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Penghui Yang, Jiaqi Yang, Xinyu Zeng, Huajian Yang, Junbo Zhong
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Abstract

Introducing vacancies on g-C3N4 is considered an effective strategy to enhance photocatalytic performance. However, introducing vacancies by a mild and efficient approach still remains a significant challenge in the field of photocatalysis. In this study, g-C3N4 photocatalysts with enriched nitrogen vacancies were successfully prepared by sodium ethoxide treatment at room temperature. X-ray photoelectron spectroscopy (XPS) and low temperature electron paramagnetic resonance (EPR) demonstrate that the treatment with sodium ethoxide successfully introduces nitrogen vacancies. The photoelectrochemical experiments confirm that introduction of nitrogen vacancies modulates the band structure of g-C3N4 and accelerates the separation of photogenerated charges. Additionally, nitrogen vacancies serve as effective active sites and adsorption centers for target molecules, facilitating the reaction of electrons with the target molecules and significantly boosting photocatalytic efficiency. Under irradiation of a 300 W xenon lamp, the 9GCN sample treated by 9 g of sodium ethoxide exhibits the best photocatalytic performance. The conversion rate of CO2 into CO and CH4 is 3.07 and 8.58 times higher than that on the single sample, respectively. In situ diffuse reflectance Fourier-transform infrared spectroscopy (DRIFTS) confirms the dynamic process of CO2 conversion to CO and CH4. Additionally, result of photocatalytic reduction of Cr(VI) further confirms the versatility of the photocatalyst. This work provides a practical pathway for the development of defective g-C3N4 photocatalysts for applications in carbon cycling and environmental purification.
乙醇钠处理诱导g-C3N4上富集氮空位,从而实现光催化CO2还原和Cr(VI)去除
在g-C3N4上引入空位被认为是提高光催化性能的有效策略。然而,如何以温和而有效的方法引入空位仍然是光催化领域的一个重大挑战。本研究在室温下,通过乙氧基钠处理,成功制备了富氮空位的g-C3N4光催化剂。x射线光电子能谱(XPS)和低温电子顺磁共振(EPR)结果表明,乙氧化钠处理成功地引入了氮空位。光电化学实验证实,氮空位的引入调节了g-C3N4的能带结构,加速了光生电荷的分离。此外,氮空位作为靶分子的有效活性位点和吸附中心,促进了电子与靶分子的反应,显著提高了光催化效率。在300 W氙灯照射下,9GCN样品经9g乙氧基钠处理后表现出最佳的光催化性能。与单一样品相比,CO2转化为CO和CH4的速率分别提高了3.07倍和8.58倍。原位漫反射傅里叶变换红外光谱(DRIFTS)证实了CO2转化为CO和CH4的动态过程。此外,光催化还原Cr(VI)的结果进一步证实了光催化剂的多功能性。本研究为开发有缺陷的g-C3N4光催化剂用于碳循环和环境净化提供了一条实用途径。
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来源期刊
Journal of Physics and Chemistry of Solids
Journal of Physics and Chemistry of Solids 工程技术-化学综合
CiteScore
7.80
自引率
2.50%
发文量
605
审稿时长
40 days
期刊介绍: The Journal of Physics and Chemistry of Solids is a well-established international medium for publication of archival research in condensed matter and materials sciences. Areas of interest broadly include experimental and theoretical research on electronic, magnetic, spectroscopic and structural properties as well as the statistical mechanics and thermodynamics of materials. The focus is on gaining physical and chemical insight into the properties and potential applications of condensed matter systems. Within the broad scope of the journal, beyond regular contributions, the editors have identified submissions in the following areas of physics and chemistry of solids to be of special current interest to the journal: Low-dimensional systems Exotic states of quantum electron matter including topological phases Energy conversion and storage Interfaces, nanoparticles and catalysts.
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