Kinetics-Driven Dual Hydrogen Spillover Effects for Ultrasensitive Hydrogen Sensing

被引:21
作者
Cai, Haijie [1 ]
Luo, Na [1 ]
Wang, Xiaowu [1 ]
Guo, Mengmeng [1 ]
Li, Xiaojie [1 ]
Lu, Bo [2 ]
Xue, Zhenggang [1 ]
Xu, Jiaqiang [1 ]
机构
[1] Shanghai Univ, Coll Sci, Dept Phys, Dept Chem,NEST Lab, Shanghai 200444, Peoples R China
[2] Shanghai Univ, Instrumental Anal & Res Ctr, Shanghai 200444, Peoples R China
基金
中国国家自然科学基金;
关键词
buffer-cavity structures; dual hydrogen spillover; hydrogen sensors; kinetics-driven; HOLLOW MICROSPHERES; SENSORS; NANOPARTICLES; NANOSHEETS; NANOWIRES;
D O I
10.1002/smll.202302652
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Palladium (Pd)-modified metal oxide semiconductors (MOSs) gas sensors often exhibit unexpected hydrogen (H-2) sensing activity through a spillover effect. However, sluggish kinetics over a limited Pd-MOS surface seriously restrict the sensing process. Here, a hollow Pd-NiO/SnO2 buffered nanocavity is engineered to kinetically drive the H-2 spillover over dual yolk-shell surface for the ultrasensitive H-2 sensing. This unique nanocavity is found and can induce more H-2 absorption and markedly improve kinetical H-2 ab/desorption rates. Meanwhile, the limited buffer-room allows the H-2 molecules to adequately spillover in the inside-layer surface and thus realize dual H-2 spillover effect. Ex situ XPS, in situ Raman, and density functional theory (DFT) analysis further confirm that the Pd species can effectively combine H-2 to form Pd-H bonds and then dissociate the hydrogen species to NiO/SnO2 surface. The final Pd-NiO/SnO2 sensors exhibit an ultrasensitive response (0.1-1000 ppm H-2) and low actual detection limit (100 ppb) at the operating temperature of 230 & DEG;C, which surpass that of most reported H-2 sensors.
引用
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页数:10
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