Creating Atomically Iridium-Doped PdOx Nanoparticles for Efficient and Durable Methane Abatement

被引:7
|
作者
Wang, Yingjie [1 ,3 ]
Xu, Guangyan [1 ,2 ]
Sun, Yanwei [1 ,2 ]
Shi, Wei [1 ,2 ]
Shi, Xiaoyan [1 ,2 ]
Yu, Yunbo [1 ,2 ,3 ]
He, Hong [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Res Ctr Ecoenvironm Sci, State Key Joint Lab Environm Simulat & Pollut Cont, Beijing 100085, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Ganjiang Innovat Acad, Ganzhou 341000, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
methane combustion; C-Hactivation; PdOx nanoparticles; single-atom regulation; antisintering; H BOND ACTIVATION; ACTIVE-SITES; OXIDATION; PALLADIUM; COMBUSTION; CATALYSTS; SURFACE; CH4; DEHYDROGENATION; ETHANE;
D O I
10.1021/acs.est.4c00868
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The urgent environmental concern of methane abatement, attributed to its high global warming potential, necessitates the development of methane oxidation catalysts (MOC) with enhanced low-temperature activity and durability. Herein, an iridium-doped PdOx nanoparticle supported on silicalite-1 zeolite (PdIr/S-1) catalyst was synthesized and applied for methane catalytic combustion. Comprehensive characterizations confirmed the atomically dispersed nature of iridium on the surface of PdOx nanoparticles, creating an Ir-4f-O-Pd-cus microstructure. The atomically doped Ir transferred more electrons to adjacent oxygen atoms, modifying the electronic structure of PdOx and thus enhancing the redox ability of the PdIr/S-1 catalysts. This electronic modulation facilitated methane adsorption on the Pd site of Ir-4f-O-Pd-cus, reducing the energy barrier for C-H bond cleavage and thereby increasing the reaction rate for methane oxidation. Consequently, the optimized PdIr0.1/S-1 showed outstanding low-temperature activity for methane combustion (T-50 = 276 degrees C) after aging and maintained long-term stability over 100 h under simulated exhaust conditions. Remarkably, the novel PdIr0.1/S-1 catalyst demonstrated significantly enhanced activity even after undergoing harsh hydrothermal aging at 750 degrees C for 16 h, significantly outperforming the conventional Pd/Al2O3 catalyst. This work provides valuable insights for designing efficient and durable MOC catalysts, addressing the critical issue of methane abatement.
引用
收藏
页码:10357 / 10367
页数:11
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