Department of Materials Science and Engineering, City University of Hong Kong, Hong Kong SAR, PR China.
Department of Materials Science and Engineering, City University of Hong Kong, Hong Kong SAR, PR China.
Biosens Bioelectron. 2018 May 30;106:129-135. doi: 10.1016/j.bios.2018.02.006. Epub 2018 Feb 3.
In this report, titanium nitride thin film synthesized with reactive magneto-sputtering technique is proposed as an alternative surface plasmon resonance sensing material. The physical and chemical natures were initially studied by atomic force microscopy, X-ray diffraction and X-ray photoelectron spectroscopy. In virtue of white-light common-path sensing system, the wavelength modulated TiN films achieved tunable evanescent plasmonic field from 573 nm to 627 nm. The optimized TiN film with 29.8 nm thickness exhibited good differential phase sensitivity (i.e. 1.932 × 10 RIU) to refractive index alteration, which is comparable to the performance of gold film. We have also attained direct measurement of biotin adsorption on the TiN and monitored sub-sequential biotin-streptavidin conjugation. It was found that TiN films have significantly higher binding affinity toward biotin than that of gold in experiments, so we are able to detect biotin directly to 0.22 µg/ml (0.90 µM) in label-free manner. The adsorption mechanism of biotin on TiN(200) are also explored with periodic density functional theory (DFT) via computer simulation and it was found that the exceptional biotin-TiN affinity may be due to the stacking formation of both N-Ti and O-Ti bonds. Also, the adsorption energy of biotin-TiN was found to be - 1.85 eV, which was two times higher than that of biotin-gold. Both experimental and computational results indicate, for the first time, that the TiN film can be directly functionalized with biotin molecules, thus it serves as an alternative plasmonic material to existing gold-based SPR biosensors.
在本报告中,提出了一种使用反应磁控溅射技术合成的氮化钛薄膜作为替代表面等离子体共振传感材料。通过原子力显微镜、X 射线衍射和 X 射线光电子能谱对其物理和化学性质进行了初步研究。借助白光共路传感系统,实现了可调谐的氮化钛薄膜消逝等离子体激元场,波长范围为 573nm 至 627nm。具有 29.8nm 厚度的优化氮化钛薄膜对折射率变化表现出良好的差分相位灵敏度(即 1.932×10RIU),与金膜的性能相当。我们还实现了对氮化钛上生物素吸附的直接测量,并监测了随后的生物素-链霉亲和素偶联。实验发现,氮化钛薄膜对生物素的结合亲和力明显高于金,因此我们能够以无标记的方式直接检测到 0.22µg/ml(0.90µM)的生物素。通过计算机模拟进行周期性密度泛函理论(DFT)计算,还探索了生物素在氮化钛(200)上的吸附机制,发现生物素与氮化钛的特殊亲和力可能归因于 N-Ti 和 O-Ti 键的堆叠形成。此外,还发现生物素-氮化钛的吸附能为-1.85eV,是生物素-金的两倍。实验和计算结果均首次表明,氮化钛薄膜可以直接与生物素分子功能化,因此它可以替代现有的基于金的 SPR 生物传感器的等离子体材料。