在纳米棒结构中生长负载镍的 CdS,以在太阳照射下实现光催化和染料降解应用

Vikash Kumar, Benjamin Raj, Parmeshwar Kommu, Sanjeet Kumar Paswan, Gajendra Prasad Singh
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引用次数: 0

摘要

由于全球能源消耗呈指数级增长,而化石燃料又导致环境状况恶化,因此,改善取之不尽、用之不竭的可持续资源至关重要。一般来说,太阳能是清洁且环保的能源之一。通过收集太阳能进行光催化,并将其视为制氢等各种能源生产应用的一种前景广阔的解决方案。在这里,我们使用硫化镉和掺杂镍的硫化镉(重量百分比分别为 0.5%、1% 和 5%)作为光催化剂进行水分裂,最终产生大量氢气(H2)。硫化镉是通过化学沉淀法制备的,而镍镉硫化物则是通过水热技术制备的。通过 X 射线衍射 (XRD) 检查了纯度和相的形成,并使用 Full Prof 软件通过 Rietveld 精炼进行了验证。场发射扫描电子显微镜(FESEM)和透射电子显微镜(TEM)光谱技术对合成材料的表面形貌和结构进行了评估。结果表明,镍含量为 1.0 wt% 的 Ni-CdS 纳米复合材料在 5 小时内的 H2 演化率最高,达到 9 mmolg-1,并且具有很强的光稳定性,比 CdS 高出约 50 倍。对该材料进行了降解有机染料的光催化测试。新制备的复合材料(CdS-Ni-NiO)被用于亚甲基蓝(MB)染料的光催化降解。Ni(1.0 wt%)-CdS 在人工太阳光下 90 分钟内的最佳降解率为 95.436。晶体生长机理表明,当掺入镍金属时,CdS 的球形结构聚集成纳米棒结构,这也从 CdS 和掺镍 CdS 的 TEM 图像中得到了验证。在 854.88 eV 和 861.07 eV 处观察到的 Ni2+ XPS 峰,能量间隔为 6.18 eV,证实了 Ni/CdS 中存在 NiO。纯 CdS 和 Ni(1.0 wt%)-CdS 纳米棒的拉曼带分别在 300 cm-1 和 293 cm-1 处观察到 1LO 声子,在 601 cm-1 和 586 cm-1 处观察到 2LO 声子。镍将 CdS 带隙从 2.36 调至 2.20 eV。这些结果为设计多组分 CdS-Ni 纳米复合材料用于高效 H2 演化和其他环境应用铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Growth of Ni loaded CdS in nanorods structure for photocatalytic and dye degradation applications under solar irradiation
Due to the exponential increase in global energy consumption and the degradation of environmental conditions caused by fossil fuels, it is critical to improve inexhaustible and sustainable resources. Generally, solar energy is one of the clean and environmentally agreeable energy sources. By harvesting solar energy for photocatalysis and considering it as a promising solution for various energy generation applications such as hydrogen production. Herein we are using Cadmium Sulphide and Nickel-doped Cadmium Sulphide in 0.5, 1 and 5 weight percent which act as photocatalyst for water splitting which will eventually produce an enormous amount of Hydrogen (H2). Cadmium sulphide was prepared through the chemical precipitation method and Ni-CdS by hydrothermal technique. The purity and phase formation were examined by the X-ray diffraction (XRD) and validated via Rietveld refinement by using Full Prof software. The surface morphology and the structure of as-synthesized material were evaluated by Field Emission Scanning Electron Microscopy (FESEM) and Transmission Electron Microscope (TEM) spectroscopic techniques. Following the results, the Ni-CdS nanocomposite having 1.0 wt% of Ni exhibits the highest H2 evolution rate of 9 mmolg−1 in 5 h with strong photo-stability, which is about 50 times higher than that of CdS. The material was tested to degrade organic dye for its photocatalytic operations. The newly prepared composite materials (CdS-Ni-NiO) were used for the photocatalytic degradation of the methylene blue (MB) dye. Ni(1.0 wt%)-CdS shows an optimal degradation percentage of 95.436 in the presence of artificial solar light in 90 min. Crystal growth mechanism shows the spherical structure of CdS agglomerate to form nanorods structure when doped with Ni metal which is also verified by the TEM images of CdS and Ni-doped CdS. The XPS peaks observed at 854.88 eV and 861.07 eV for Ni2+ with an energy separation of 6.18 eV confirmed the existence of NiO with Ni/CdS. The Raman bands of pure CdS and Ni (1.0 wt%)-CdS nanorods were observed at 300 cm-1 and 293 cm−1 for 1LO phonon and 601 cm−1 and 586 cm−1 for 2LO phonon corresponds. The Ni tuned the CdS band gap from 2.36 to 2.20 eV. The results pave the way for designing multi-component CdS-Ni nano-composites for highly efficient H2 evolution and other environmental applications.
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