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Visible-light induced photocatalysis of AgCl@Ag/titanate nanotubes/ nitrogen-doped reduced graphite oxide composites

机译:可见光诱导的AgCl @ Ag /钛酸酯纳米管/氮掺杂还原氧化石墨复合材料的光催化

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High recombination rate of photogenerated electron-hole pairs and relatively narrow photoresponsive range of TiO2-based photocatalysts are the remaining challenges for their practical applications. To address such challenges, photocatalysts consisting of AgCl covered Ag nanoparticles (AgCl@Ag), titanate nanotubes (TiNT), and nitrogen-doped reduced graphite oxide (rGON) are fabricated through alkaline hydrothermal process, followed by deposition and in situ surface-oxidation of silver nanoparticles. In the synthesized photocatalysts, the titanate nanotubes have average length of about 100 nm with inner diameters of about 5 nm and the size of the formed silver nanoparticles is in the range of 50-100 nm. The synthesized photocatalyst degrades almost all the model organic pollutant Rhodamine B in 35 min and remains 90% of photocatalytic efficiency after 5 degradation cycles under visible light irradiation. Since the oxidant FeCl3 applied for oxidation of surface Ag to AgCl is difficult to be completely removed due to the high adsorption capacity of TiNT and rGON, the effect of reside Fe atoms on photocatalytic activity is evaluated and the results reveal that the residue Fe atom only affect the initial photodegradation performance. Nevertheless, the results demonstrate that the formed composite catalyst is a promising candidate for antibiosis and remediation in aquatic environmental contamination. (C) 2018 Elsevier B.V. All rights reserved.
机译:光生电子-空穴对的高复合率和TiO 2基光催化剂的相对较窄的光响应范围是其实际应用中仍然存在的挑战。为了应对这些挑战,通过碱性水热工艺制备了由AgCl覆盖的Ag纳米颗粒(AgCl @ Ag),钛酸酯纳米管(TiNT)和氮掺杂的还原石墨氧化物(rGON)组成的光催化剂,然后进行沉积和原位表面氧化银纳米颗粒。在合成的光催化剂中,钛酸酯纳米管的平均长度为约100nm,内径为约5nm,并且形成的银纳米颗粒的尺寸在50-100nm的范围内。合成的光催化剂在35分钟内降解了几乎所有模型有机污染物若丹明B,并且在可见光照射下经过5次降解循环后仍保持90%的光催化效率。由于TiNT和rGON的高吸附能力,由于难以将用于将表面Ag氧化为AgCl的氧化剂FeCl3完全去除,因此评估了残留Fe原子对光催化活性的影响,结果表明仅残留Fe原子影响初始光降解性能。然而,结果表明,所形成的复合催化剂是水生环境污染中抗菌和修复的有前途的候选者。 (C)2018 Elsevier B.V.保留所有权利。

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