Meng Hao, Li Xiaoxue, Zhang Xia, Liu Yufeng, Xu Yan, Han Yide, Xu Junli
Department of Chemistry, College of Sciences, Northeastern University, Shenyang 110819, China.
College of Pharmacy, Liaoning University, Shenyang, 110036, China.
Dalton Trans. 2015 Dec 14;44(46):19948-55. doi: 10.1039/c5dt03869c.
Highly efficient composite photocatalysts composed of silver cyanamide (Ag2NCN) and anatase titania (TiO2) were fabricated through a chemical precipitation process of silver nitrate and cyanamide in TiO2 suspensions. The TiO2 nanoparticles around 15 nm were immobilized on the surface of rectangular Ag2NCN particles to form a hetero-structure, and the contents of TiO2 were varied to tune the structure and the photocatalytic performances. In comparison with single TiO2 or Ag2NCN, the TiO2/Ag2NCN nanocomposites exhibited a prominent improved photocatalytic activity in the hydrogen generation, and the hydrogen evolution rate (1494.0 μmol (g h)(-1)) was higher than most of the reported TiO2-composite photocatalysts. Based on the structure investigation, the photocatalytic mechanism of these TiO2/Ag2NCN nanocomposites was proposed. The enhanced photocatalytic activity was attributed to three points: the matched energy level between TiO2 and Ag2NCN promoted the electron-hole transfer and thus inhibited the recombination of photogenerated electrons and holes; the great electron storage capacity of metallic silver produced in the photocatalytic process also facilitated the charge separation; in addition, the expanded absorption spectrum because of the composite structure enhanced the UV and visible light response ability. These TiO2/Ag2NCN nanocomposites also presented good photocatalytic stability in the typical cycle tests. This work provided new insights into fabricating highly efficient composite photocatalysts containing silver and TiO2 for hydrogen generation.
通过在二氧化钛(TiO₂)悬浮液中硝酸银和氰胺的化学沉淀过程,制备了由氰胺化银(Ag₂NCN)和锐钛矿型二氧化钛(TiO₂)组成的高效复合光催化剂。约15纳米的TiO₂纳米颗粒固定在矩形Ag₂NCN颗粒表面形成异质结构,并改变TiO₂的含量以调节结构和光催化性能。与单一的TiO₂或Ag₂NCN相比,TiO₂/Ag₂NCN纳米复合材料在产氢方面表现出显著提高的光催化活性,析氢速率(1494.0 μmol (g h)(⁻¹))高于大多数已报道的TiO₂复合光催化剂。基于结构研究,提出了这些TiO₂/Ag₂NCN纳米复合材料的光催化机理。光催化活性增强归因于三点:TiO₂和Ag₂NCN之间匹配的能级促进了电子 - 空穴转移,从而抑制了光生电子和空穴的复合;光催化过程中产生的金属银的巨大电子存储容量也促进了电荷分离;此外,复合结构导致的吸收光谱扩展增强了紫外和可见光响应能力。这些TiO₂/Ag₂NCN纳米复合材料在典型的循环测试中也表现出良好的光催化稳定性。这项工作为制备用于产氢的含银和TiO₂的高效复合光催化剂提供了新的见解。