用于改善盐酸四环素降解的过渡金属镍纳米颗粒装饰 g-C3N4 光催化剂

IF 4.1 3区化学 Q2 CHEMISTRY, PHYSICAL

Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2024-09-24 DOI:10.1016/j.jphotochem.2024.116042

Oanh T.K. Nguyen , Vinh Huu Nguyen , Linh Xuan Nong , Que-Minh T. Doan , Lan-Anh T. Hoang , Kwang Hee Nam , Taeyoon Lee , Trinh Duy Nguyen

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引用次数: 0

摘要

在 N,N-二甲基甲酰胺溶剂中利用溶热技术开发了金属镍纳米粒子（Ni0 NPs）支撑的 g-C3N4。在 g-C3N4 光催化剂上均匀分散的 Ni0 NPs 可以提高光催化效率。优化后的 Ni/g-C3N4 催化剂在 LED 光照射下对 TCH 的光降解率高达 6.0 × 10-3 min-1，约为裸 g-C3N4 催化剂的三倍。这一优异性能源于 Ni0 NPs 与宿主 g-C3N4 之间的强相互作用促进了电子-空穴对的分离，光学和电化学性能分析也证明了这一点。我们的工作为利用异质结光催化剂有效降解污染物提供了一种简便的方法。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Transition metal nickel nanoparticle-decorated g-C3N4 photocatalyst for improving tetracycline hydrochloride degradation

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Transition metal nickel nanoparticle-decorated g-C3N4 photocatalyst for improving tetracycline hydrochloride degradation

Metallic nickel nanoparticles (Ni⁰ NPs)-supported g-C₃N₄ have been developed using a solvothermal technique in N,N-dimethylformamide solvent. A uniformly dispersion of Ni⁰ NPs anchored on a g-C₃N₄ photocatalyst can improve the photocatalytic efficiency. The optimized Ni/g-C₃N₄ catalyst demonstrated a high photodegradation rate of TCH at 6.0 × 10⁻³ min⁻¹ under LED light irradiation, which was approximately three times greater than that of the bare g-C₃N₄ catalyst. This superior performance originates from the capable separation of electron-hole pairs, facilitated by the strong interaction between Ni⁰ NPs and the host g-C₃N₄, as supported by optical and electrochemical property analysis. Our work provides a facile manner for the effective degradation of pollutants using heterojunction photocatalysts.

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来源期刊

Journal of Photochemistry and Photobiology A-chemistry 化学-物理化学

CiteScore

7.90

自引率

7.00%

发文量

580

审稿时长

48 days

期刊介绍： JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.