ACS sensors · 2026
TiO2/SnO2-Pt Janus-Type Nanofibers with Gradient Band Distribution for Enhanced Room-Temperature NO2 Detection via Cascade Photo-Generated Charge Transfer.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Wu Xinyu, Li Xiaowei, Cheng Wanying, Chen Xianglin, Yin Yunpeng, Zeng Yang, Han Chaohan, Shao Changlu, Liu Yichun
Аннотация
Room-temperature metal oxide semiconductor (MOS) gas sensors enabled by photoexcitation have demonstrated significant potential in various applications due to their outstanding advantages, such as the absence of heating requirements, low power consumption, and high safety. However, conventional MOS often suffers from inefficient charge separation and rapid recombination of photogenerated carriers, which significantly hamper the sensing performance of photoexcited MOS gas sensors. Here, we designed ternary TiO2/SnO2-Pt Janus-type heterojunction nanofibers (JHNFs) with a gradient band distribution for high-performance NO2 detection. The structurally ordered, one-dimensional nanofiber architecture largely promotes efficient and directional transport of photogenerated carriers. The gradient band distribution of the TiO2/SnO2-Pt JHNFs facilitates a cascade charge transfer pathway, synergistically enhancing photogenerated carrier utilization and surface NO2 adsorption. Under room-temperature UV excitation, the sensors based on TiO2/SnO2-Pt JHNFs demonstrate a much higher response to NO2 compared to pure SnO2 (5.3-fold enhancement) and TiO2 (6.7-fold enhancement) counterparts. In addition, the sensor achieves a low detection limit of 50 ppb, rapid response/recovery, and excellent long-term stability. Our findings not only systematically unravel the relationship between gas sensing performance and photogenerated carrier separation but also establish a feasible design strategy for developing high-performance photoactivated room-temperature gas sensors.