School of Materials Science and Engineering, South China University of Technology, Guangzhou 510640, China.
ACS Sens. 2024 Jan 26;9(1):195-205. doi: 10.1021/acssensors.3c01825. Epub 2024 Jan 2.
A NO sensor with a detection limit down to the ppb level based on pristine SnO has been developed through a facile poly(acrylic acid)-mediated hydrothermal method. SnO particles of solid microsphere, hollow microsphere, and nanosphere morphologies were synthesized, with respective constitutional crystallite of size ∼2 μm in length and 10-20 nm and ∼7 nm in diameter. All sensors show great selectivity to NO. The hollow microsphere sensor exhibits the best performance, with medium specific surface area (SSA), followed by the nanosphere sensor with the largest SSA. This is attributed to the superposition of two opposite effects on sensor response with increased SSA: more adsorption sites and fewer electrons to be taken out with overly small crystallite that may reach complete depletion. O is found to speed up the response and recovery times but reduce the response because O adsorbates facilitate the adsorption/desorption of NO thermodynamically, and the two oxidizing gases compete in harvesting electrons from SnO. The adverse effect of humidity can be minimized by operating the sensor at 110 °C. The response of the hollow microsphere sensor to 50 ppb of NO is 8.8 (/) at room temperature, and it increases to 15.1 at 110 °C. These findings are useful for developing other oxidizing gas semiconductor sensors.
通过简便的聚(丙烯酸)介导的水热法,开发了一种基于原始 SnO 的检测限低至 ppb 级别的 NO 传感器。合成了具有固态微球、空心微球和纳米球形态的 SnO 颗粒,各自的晶体结构尺寸约为 2 μm 长和 10-20 nm 和 7 nm 直径。所有传感器对 NO 表现出很高的选择性。空心微球传感器表现出最佳的性能,具有中等比表面积(SSA),其次是比表面积最大的纳米球传感器。这归因于增加 SSA 对传感器响应的两个相反效应的叠加:更多的吸附位点和由于过小的晶体结构可能达到完全耗尽而导致的更少的电子被取出。O 被发现可以加速响应和恢复时间,但由于 O 吸附物促进了 NO 的吸附/解吸,热力学上有利于吸附/解吸,两种氧化气体在从 SnO 中获取电子方面存在竞争,从而降低了响应。通过在 110°C 下操作传感器,可以将湿度的不利影响降至最低。空心微球传感器在室温下对 50 ppb 的 NO 的响应为 8.8 (/), 在 110°C 时增加到 15.1。这些发现对于开发其他氧化气体半导体传感器非常有用。