硫化氢
纳米技术
导电体
材料科学
金属有机骨架
氧化还原
氧化物
纳米晶
危险废物
原位
化学
氢
金属
配体(生物化学)
检出限
光学传感
生物传感器
硫化物
分辨率(逻辑)
一氧化碳
化学工程
高分辨率
分子
工作(物理)
二氧化硫
氨
有毒气体
作者
Elissa O. Shehayeb,Joseph Y. M. Chan,Doran L. Pennington,Christopher H. Hendon,Katherine A. Mirica
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-06-10
卷期号:20 (24): 17233-17243
标识
DOI:10.1021/acsnano.5c19929
摘要
High Resolution Image Download MS PowerPoint Slide Despite advances in gas sensing technologies, achieving rapid detection and differentiation of toxic gases remains a critical challenge. Herein, three conductive metal–organic frameworks (cMOFs) based on metallotetrapyrazinoporphyrazine (MTPz) ligands are utilized to enable distinct chemiresistive sensing toward hazardous gases within seconds of exposure. This study focuses on harnessing variations in material–analyte interactions upon tuning the central metal within MTPz ligand (M = Co, Ni, Cu), to achieve discrete sensing responses capable of identifying hydrogen sulfide (H 2 S), ammonia (NH 3 ), sulfur dioxide (SO 2 ), and nitric oxide (NO), with detection limits as low as 0.7, 0.6, 2.5, and 0.03 ppm, respectively, within 6 seconds of gas exposure. The sensor array differentiates these gases at concentrations exceeding their permissible exposure limits within seconds. Complementary in situ and ex situ spectroscopic analyses reveal distinct redox processes governing the varied sensing responses, underscoring the critical role of molecular design in optimizing performance. This work establishes a framework for tailoring molecular design strategies toward next-generation gas sensing materials.
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