Urs Kusuma, Carey Tian, Tsetseris Leonidas, Liu Shixin, Synnatschke Kevin, Sofer Zdeněk, Coleman Jonathan N, Wenger John Charles, Biswas Subhajit, Holmes Justin D
School of Chemistry, University College Cork, Cork T12 YN60, Ireland.
AMBER Centre, Environmental Research Institute, University College Cork, Cork T23 XE10, Ireland.
ACS Appl Nano Mater. 2025 Jan 24;8(5):2141-2152. doi: 10.1021/acsanm.4c05066. eCollection 2025 Feb 7.
Nitrogen dioxide (NO) is a gaseous air pollutant linked to respiratory and cardiovascular diseases and environmental problems such as acid rain and tropospheric ozone formation. Reference instruments for measuring NO are expensive, highlighting the need to develop low cost sensor technologies for wider scale monitoring of this critical pollutant. Here, we report the development of a scalable sensor using electrochemically exfoliated 2D molybdenum disulfide (MoS) networks. The sensor can detect a wide range of NO concentrations at room temperature, with an experimental limit of detection (LOD) as low as 150 ppb and a theoretical LOD of 1.9 parts per quadrillion (ppq) in dry air. The sensor exhibited approximately 90% response to 1 ppm of NO within 10 min of exposure. UV irradiation significantly enhanced the sensor's recovery time, reducing it from 20 min to less than 2 min. Evaluation of the sensor within a large (∼6.5 m) atmospheric simulation chamber yielded a similar response and recovery time performance, opening the opportunity for further tests in the chamber under various conditions. Finally, using Density Functional Theory (DFT) calculations, we identified key atomic-scale structures and processes highlighting the importance of electrochemically exfoliated sulfur-deficient MoS for sensitive room temperature NO detection.
二氧化氮(NO)是一种气态空气污染物,与呼吸道和心血管疾病以及酸雨和对流层臭氧形成等环境问题有关。用于测量NO的参考仪器价格昂贵,这凸显了开发低成本传感器技术以更广泛地监测这种关键污染物的必要性。在此,我们报告了一种使用电化学剥离的二维二硫化钼(MoS)网络开发的可扩展传感器。该传感器在室温下可检测广泛的NO浓度范围,实验检测限(LOD)低至150 ppb,在干燥空气中的理论LOD为万亿分之一(ppq)的1.9 。该传感器在暴露于1 ppm的NO 10分钟内表现出约90%的响应。紫外线照射显著提高了传感器的恢复时间,从20分钟减少到不到2分钟。在大型(约6.5米)大气模拟室内对该传感器进行评估,得到了类似的响应和恢复时间性能,为在该室内进行各种条件下的进一步测试提供了机会。最后,通过密度泛函理论(DFT)计算,我们确定了关键的原子尺度结构和过程,突出了电化学剥离的缺硫MoS对灵敏室温NO检测的重要性。