Detecting the Genesis of a High-Performance Carbon-Supported Pd Sulfide Nanophase and Its Evolution in the Hydrogenation of Butadiene

ACS Catalysis ◽  
2015 ◽  
Vol 5 (9) ◽  
pp. 5235-5241 ◽  
Author(s):  
Belén Bachiller-Baeza ◽  
Ana Iglesias-Juez ◽  
Eva Castillejos-López ◽  
Antonio Guerrero-Ruiz ◽  
Marco Di Michiel ◽  
...  
Catalysts ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 802
Author(s):  
Chang Sun ◽  
Yingxin Mu ◽  
Yuxin Wang

Electrochemical ammonia synthesis, which is an alternative approach to the Haber–Bosch process, has attracted the attention of researchers because of its advantages including mild working conditions, environmental protection, and simple process. However, the biggest problem in this field is the lack of high-performance catalysts. Here, we report high-efficiency electroreduction of N2 to NH3 on γ-MnO2-supported Pd nanoparticles (Pd/γ-MnO2) under ambient conditions, which exhibits excellent catalytic activity with an NH3 yield rate of 19.72 μg·mg−1Pd h−1 and a Faradaic efficiency of 8.4% at −0.05 V vs. the reversible hydrogen electrode (RHE). X-ray diffraction (XRD) and transmission electron microscopy (TEM) characterization shows that Pd nanoparticles are homogeneously dispersed on the γ-MnO2. Pd/γ-MnO2 outperforms other catalysts including Pd/C and γ-MnO2 because of its synergistic catalytic effect between Pd and Mn.


2017 ◽  
Vol 807 ◽  
pp. 220-227 ◽  
Author(s):  
Zhen Chen ◽  
Bo Zhao ◽  
Xian-Zhu Fu ◽  
Rong Sun ◽  
Ching-Ping Wong

2019 ◽  
Vol 7 (6) ◽  
pp. 2660-2666 ◽  
Author(s):  
Pengyao Ju ◽  
Shujie Wu ◽  
Qing Su ◽  
Xiaodong Li ◽  
Ziqian Liu ◽  
...  

Salen–porphyrin-based CMP supported Pd nanoparticles were employed as high-performance heterogeneous catalysts for aqueous Suzuki–Miyaura and Heck–Mizoroki coupling reactions.


2018 ◽  
Vol 42 (2) ◽  
pp. 812-816 ◽  
Author(s):  
Debkumar Nandi ◽  
Rafique Ul Islam ◽  
Nishu Devi ◽  
Samarjeet Siwal ◽  
Kaushik Mallick

A carbon nitride-supported Pd nanoparticle-catalyzed C–N cross coupling reaction.


Energy ◽  
2017 ◽  
Vol 127 ◽  
pp. 419-427 ◽  
Author(s):  
Leyla Abolghasemi Fard ◽  
Reza Ojani ◽  
Jahan Bakhsh Raoof ◽  
Ehsan Nazarzadeh Zare ◽  
Moslem Mansour Lakouraj

Materials ◽  
2020 ◽  
Vol 13 (3) ◽  
pp. 691
Author(s):  
Tibo De Saegher ◽  
Jeroen Lauwaert ◽  
Jorku Hanssen ◽  
Els Bruneel ◽  
Matthias Van Zele ◽  
...  

Monometallic cerium layered double hydroxides (Ce-LDH) supports were successfully synthesized by a homogeneous alkalization route driven by hexamethylenetetramine (HMT). The formation of the Ce-LDH was confirmed and its structural and compositional properties studied by XRD, SEM, XPS, iodometric analyses and TGA. HT-XRD, N2-sorption and XRF analyses revealed that by increasing the calcination temperature from 200 to 800 °C, the Ce-LDH material transforms to ceria (CeO2) in four distinct phases, i.e., the loss of intramolecular water, dehydroxylation, removal of nitrate groups and removal of sulfate groups. When loaded with 2.5 wt% palladium (Pd) and 2.5 wt% nickel (Ni) and calcined at 500 °C, the PdNi-Ce-LDH-derived catalysts strongly outperform the PdNi-CeO2 benchmark catalyst in terms of conversion as well as selectivity for the hydrogenolysis of benzyl phenyl ether (BPE), a model compound for the α-O-4 ether linkage in lignin. The PdNi-Ce-LDH catalysts showed full selectivity towards phenol and toluene while the PdNi-CeO2 catalysts showed additional oxidation of toluene to benzoic acid. The highest BPE conversion was observed with the PdNi-Ce-LDH catalyst calcined at 600 °C, which could be related to an optimum in morphological and compositional characteristics of the support.


Author(s):  
Shuai Yang ◽  
Yuli Chen ◽  
Shuaijian Huang ◽  
Lu Deng ◽  
Yuanyuan Wu ◽  
...  

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