Boosting Interfacial Electron Transfer between Pd and ZnTi-LDH via Defect Induction for Enhanced Metal–Support Interaction in CO Direct Esterification Reaction

Author(s):  
Kai-Qiang Jing ◽  
Yu-Qing Fu ◽  
Zhe-Ning Chen ◽  
Teng Zhang ◽  
Jing Sun ◽  
...  
2016 ◽  
Vol 6 (9) ◽  
pp. 3220-3229 ◽  
Author(s):  
Alberto Naldoni ◽  
Francesca Riboni ◽  
Marcello Marelli ◽  
Filippo Bossola ◽  
Giacomo Ulisse ◽  
...  

Photocatalytic oxidations promoted by hot electron transfer and PRET strongly depend on Au loading and SMSI.


2021 ◽  
Author(s):  
Liang Wei ◽  
Jian Chen ◽  
Shuai Lyu ◽  
Chengchao Liu ◽  
Yanxi Zhao ◽  
...  

The delicate balance between dispersion and reduction of the Co-based Fischer–Tropsch synthesis catalyst is the golden key to enhancing catalytic performance, which highly depends on an optimized metal–support interaction. In...


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yi Shi ◽  
Zhi-Rui Ma ◽  
Yi-Ying Xiao ◽  
Yun-Chao Yin ◽  
Wen-Mao Huang ◽  
...  

AbstractTuning metal–support interaction has been considered as an effective approach to modulate the electronic structure and catalytic activity of supported metal catalysts. At the atomic level, the understanding of the structure–activity relationship still remains obscure in heterogeneous catalysis, such as the conversion of water (alkaline) or hydronium ions (acid) to hydrogen (hydrogen evolution reaction, HER). Here, we reveal that the fine control over the oxidation states of single-atom Pt catalysts through electronic metal–support interaction significantly modulates the catalytic activities in either acidic or alkaline HER. Combined with detailed spectroscopic and electrochemical characterizations, the structure–activity relationship is established by correlating the acidic/alkaline HER activity with the average oxidation state of single-atom Pt and the Pt–H/Pt–OH interaction. This study sheds light on the atomic-level mechanistic understanding of acidic and alkaline HER, and further provides guidelines for the rational design of high-performance single-atom catalysts.


Nanoscale ◽  
2020 ◽  
Vol 12 (27) ◽  
pp. 14825-14830
Author(s):  
Kai-Qiang Jing ◽  
Yu-Qing Fu ◽  
Zhi-Qiao Wang ◽  
Zhe-Ning Chen ◽  
Hong-Zi Tan ◽  
...  

Zn2+-Modified MgAl-LDH with ultra-low Pd cluster loading was synthesized. The higher adsorption energy and strong covalent metal–support interaction via forming Pd–Zn bonds over Pd/ZnMgAl-LDH account for the robust catalytic performance.


2021 ◽  
Vol 45 (12) ◽  
pp. 5704-5711
Author(s):  
Luming Wu ◽  
Yu Hao ◽  
Shaohua Chen ◽  
Rui Chen ◽  
Pingchuan Sun ◽  
...  

Rare earth metal doped ZrO2 can promote the formation of oxygen vacancies in zirconia, which enhances the metal–support interaction, finally promoting catalytic activity of FA dehydrogenation.


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