材料科学
钝化
纳米棒
卤化物
纳米结构
钙钛矿(结构)
纳米技术
紫外线
纳米晶
光电探测器
光电子学
可见光谱
多孔性
氧化物
纳米线
平面的
纳米
纳米颗粒
制作
异质结
化学工程
光活性层
二氧化钛
金属
限制
光致发光
作者
Yeonji Yuk,Dokyum Kim,Jun‐Cheol Park,Yoonsung Jung,Inhyeok Oh,Donghyeon Lee,Yejoon Kim,Ji‐Eun Yeo,Young Min Song,Chang‐Lyoul Lee,Sanghan Lee
标识
DOI:10.1002/adfm.202526329
摘要
ABSTRACT Metal oxide (MO x )‐based NO 2 gas sensors typically require high temperatures or ultraviolet light, limiting their practical use. To enable visible‐light activation at room temperature, efficient and stable photosensitizers should be integrated with nanostructured MO x hosts. Halide perovskites (HP) have gained attention as promising visible‐light photosensitizers due to their excellent optoelectronic properties. However, the structural stability of HP remains a critical barrier to practical implementation, necessitating robust passivation strategies that ensure both long‐term durability and efficient interfacial charge transport. Herein, we present a novel strategy in which CsPbBr 3 nanocrystals (NCs) are encapsulated with an ultra‐thin (∼2 nm) SiO 2 shell and integrated onto structurally engineered porous SnO 2 nanorods (NRs). The sensor exhibits 13‐fold and 30‐fold enhancement in response to 10 ppm NO 2 gas under green light, compared to dark conditions and planar SnO 2 , respectively. Furthermore, the SiO 2 encapsulation enables the CsPbBr 3 NCs to maintain long‐term stability as photosensitizers for over 5 weeks, which is an unprecedented duration among visible light‐activated gas sensors. Our results demonstrate the synergistic effect of surface defect passivation and nanostructure engineering, providing a robust design strategy for realizing highly stable and high‐performance gas sensors based on HP photosensitizers and nanostructured MO x hosts under visible light.
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