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Visible-Light Driven Ni-Incorporated CdS Photocatalytic Activities for Azo-Bond Cleavages with Hydrogenation Reaction

机译:可见光驱动的NI成立的CDS光催化活性,用于氢化反应

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摘要

Ni-incorporated CdS (Ni-CdS) photocatalysts with different amounts of Ni dopant have been synthesized, characterized, and examined toward azo-bond cleavages in visible-light illuminated conditions. The optimum performance was achieved with a relatively low amount of Ni dopant (2% atomic mass). The azo bonds of azobenzene (AB) and methyl orange (MO) compounds were hydrogenated with the in-situ gener- ated hydrogen on Ni-CdS catalyst surfaces. The hydrogen evolution reaction was proved and measured with GC measure- ment during the photocatalytic session with an incandescent halogen lamp. Furthermore, the experimental data of UV-vis spectra analyses suggested the formation of aniline or sodium sulfanilate and p-aminodimethylaniline with the emerged peaks at ~240 nm, indicating azo-bond has been cleaved in AB or MO compounds, respectively. The catalytic performances of 2% Ni-CdS are also supported with electrical and photo- response analyses. To demonstrate the possibility of industrial application, Ni-CdS catalyst stability is also tested for several runs in reusability experiments and examined with cyclic voltammetry for 100 cycles without any significant degradation. The cleavage mechanisms of azo bonds in AB and MO compounds were discussed and proposed in this work.
机译:在可见光的照明条件下,已经合成,表征和检查了具有不同量的Ni掺杂剂的NI掺入的CD(NI-CDS)光催化剂。使用相对较低的Ni掺杂剂(2%原子质量)实现了最佳性能。偶氮苯(AB)和甲基橙(MO)化合物的偶氮键用Ni-CDS催化剂表面上的原位生成氢氢化。在光催化疗程中用白炽灯卤素灯在光催化疗程中证明并用GC测量证明了氢的进化反应。此外,UV-VIS光谱分析的实验数据表明,在〜240 nm处出现的峰,形成苯胺或硫钠硫酸钠和p-氨基二甲基苯胺,表明偶氮键在AB或MO化合物中分别裂解。电气和光反应分析也支持2%Ni-CD的催化性能。为了证明工业应用的可能性,还测试了Ni-CDS催化剂稳定性的可重复性实验中的多次运行,并使用循环伏安法检查100个循环,没有任何显着降解。在这项工作中讨论并提出了AB和MO化合物中偶氮键的切割机制。

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