化学
纳米棒
选择性
催化作用
贵金属
金属
纳米颗粒
氧化物
化学工程
纳米技术
有机化学
材料科学
工程类
作者
Qian Liu,Yingyi Wen,Jian-Ze Xiao,Shao-Zhen Luo,Guan-E Wang,Pengyi Tang,Xiao-Liang Ye,Gang Xu
出处
期刊:Chinese Journal of Structural Chemistry
日期:2023-06-01
卷期号:42 (6): 100069-100069
标识
DOI:10.1016/j.cjsc.2023.100069
摘要
The poor sensitivity of metal-oxide (MO) sensing material at room temperature can be enhanced by the modification of noble metal catalysts. However, the large size and uncontrollable morphology of metal nanoparticles (NPs) compromise the catalytic activity and selectivity. Downsizing metal NPs to the atomic level is a promising solution because it offers high activity and selectivity. Nevertheless, a facile and universal approach for stable loading atomic-level metal on MO-based sensing materials is still challenging. Herein, we present a strategy to construct synergetic coordination interface for uniform loading of atomic-level metal catalysts on MO-based gas-sensing materials using a difunctional mediator layer. In this work, atomically dispersed Pt catalysts are coordinately anchored on ZnO nanorods (NRs) using polydopamine (PDA) as a mediator. As a result, compared with pristine ZnO NRs, a six-fold enhanced response of 18,489% is achieved toward 100 ppm NO2 on 0.20 wt%Pt–[email protected] nm, and the selectivity is also promoted. Such sensitivity is higher than that of most reported noble metal-modified MO NO2-sensing materials. This work provides a simple and general strategy for building highly sensitive and selective gas-sensing materials using atomic-level noble metal catalyst.
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