纳米棒
X射线光电子能谱
材料科学
丙酮
吸附
多孔性
化学工程
铂金
催化作用
密度泛函理论
原子层沉积
纳米技术
图层(电子)
物理化学
有机化学
计算化学
复合材料
化学
工程类
作者
Zhenliang Dong,Qingmin Hu,Tiange Gao,Jinzheng Wang,Jiawei Kong,J. Li,Liwen Mao,Wu Cuixia,Jiaqiang Xu
标识
DOI:10.1016/j.ceramint.2024.01.072
摘要
Highly dispersed isolated sites offer opportunities to rationally design sensing materials with desired performance, but their stability under harsh reaction conditions is still challenging. Herein, we deposited the highly dispersed atomic layer deposition (ALD) platinum (Pt) species into optimized porous SnO2 nanorods derived from the Sn-based metal organic frameworks (MOFs). With confining isolated Pt into porous SnO2, the optimum operating temperature of the sensor based on SnO2–Pt2 nanorods was decreased from 275 °C to 190 °C. And the response (Ra/Rg) to 5 ppm acetone was improved from 2.63 to 6.33, along with the decrease of response time from 23 s to 9 s. Combined with X-ray adsorption, near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) and density functional theory (DFT) simulation, the highly dispersed Pt confined within SnO2 nanorods are confirmed to heighten the adsorption of acetone at working temperature and lower the reaction activation energy. The confined structure enriches the acetone in hole, further enhancing its adsorption on Pt. The highly dispersed isolated Pt sites and confined effects dramatically promote the sensing performance. The understanding of structure-activity relationships offers a novel strategy to design the ultrasensitive and stable acetone sensing materials, and it shows potential applications in design of other gas sensing or catalytic materials.
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