材料科学
钙钛矿(结构)
氧化还原
磁场
失真(音乐)
氧化物
检出限
灵敏度(控制系统)
电子转移
调制(音乐)
格子(音乐)
动力学
领域(数学)
催化作用
纳米晶
化学物理
超短脉冲
电子
纳米技术
铁磁性
动能
化学工程
光电子学
想象
波形
联轴节(管道)
响应时间
信号(编程语言)
氧化铁
电场
作者
Yunfei Wang,Min Zhang,Rui Li,Xiaolong Yao,Zhaofeng Wu,Fengdong Qu,Shan Qiu,Zhenjiang Li
摘要
ABSTRACT High‐performance gas sensors with extreme sensitivity and rapid response kinetics are fundamental to sub‐ppm H 2 S detection, which is crucial for environmental monitoring and industrial safety. However, most conventional rare‐earth ferrites have relatively sluggish responses at low concentrations because of thermodynamic and kinetic constraints and inherently high surface reaction barriers. Herein, a high‐entropy perovskite oxide with the composition (Gd 0.2 Tb 0.2 Dy 0.2 Ho 0.2 Er 0.2 )FeO 3 was designed and synthesized using a wet‐chemical method. The incorporation of multiple principal elements induced strong local lattice distortion and generated abundant chemically heterogeneous active sites. Furthermore, the application of an external magnetic field significantly optimized electron transfer pathways and accelerated the surface redox reaction kinetics. Our results reveal that the synergistic coupling between high‐entropy‐induced structural distortion and weak magnetic field modulation breaks the traditional response‐recovery trade‐off, yielding a 6‐fold sensitivity enhancement over conventional counterparts, an ultrafast 1.72 s recovery time, and an H 2 S detection limit of 0.5 ppm. This strategy, which integrates local coordination reconstruction with spin‐state intervention, is expected to be widely applicable to the development of next‐generation intelligent sensing systems.
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