Tandem Dehydrogenation of Ammonia Borane and Hydrogenation of Nitro/Nitrile Compounds Catalyzed by Graphene-Supported NiPd Alloy Nanoparticles

ACS Catalysis ◽  
2014 ◽  
Vol 4 (6) ◽  
pp. 1777-1782 ◽  
Author(s):  
Haydar Göksu ◽  
Sally Fae Ho ◽  
Önder Metin ◽  
Katip Korkmaz ◽  
Adriana Mendoza Garcia ◽  
...  
2021 ◽  
Author(s):  
Yating He ◽  
Ziqian Wang ◽  
Mingyue Mao ◽  
Qianggen Li ◽  
Guangyin Fan

Ru-based bimetallic alloy nanoparticles (NPs) have been demonstrated as efficiently catalytic sites for hydrogen evolution from ammonia borane (AB) hydrolysis, but their facile syntheses with ultrafine sizes and superior activity...


2015 ◽  
Vol 5 (1) ◽  
pp. 525-530 ◽  
Author(s):  
Jun Li ◽  
Qi-Long Zhu ◽  
Qiang Xu

Non-noble bimetallic CuCo alloy nanoparticles were successfully encapsulated in the pores of MIL-101 without aggregation on the external surfaces of the host framework, which exhibit excellent catalytic activity for hydrolytic dehydrogenation of ammonia borane.


RSC Advances ◽  
2016 ◽  
Vol 6 (107) ◽  
pp. 105940-105947 ◽  
Author(s):  
Daohua Sun ◽  
Pengyao Li ◽  
Bin Yang ◽  
Yan Xu ◽  
Jiale Huang ◽  
...  

Monodisperse AgPd alloy NPs showed remarkable catalytic activity towards the generation of hydrogen from the methanolysis of ammonia borane at room temperature.


Catalysts ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1009 ◽  
Author(s):  
Mingya Zhang ◽  
Xue Xiao ◽  
Yan Wu ◽  
Yue An ◽  
Lixin Xu ◽  
...  

Graphite carbon nitride (g-C3N4) supported PtNi alloy nanoparticles (NPs) were fabricated via a facile and simple impregnation and chemical reduction method and explored their catalytic performance towards hydrogen evolution from ammonia borane (AB) hydrolysis dehydrogenation. Interestingly, the resultant Pt0.5Ni0.5/g-C3N4 catalyst affords superior performance, including 100% conversion, 100% H2 selectivity, yielding the extraordinary initial total turnover frequency (TOF) of 250.8 molH2 min−1 (molPt)−1 for hydrogen evolution from AB at 10 °C, a relatively low activation energy of 38.09 kJ mol−1, and a remarkable reusability (at least 10 times), which surpass most of the noble metal heterogeneous catalysts. This notably improved activity is attributed to the charge interaction between PtNi NPs and g-C3N4 support. Especially, the nitrogen-containing functional groups on g-C3N4, serving as the anchoring sites for PtNi NPs, may be beneficial for becoming a uniform distribution and decreasing the particle size for the NPs. Our work not only provides a cost-effective route for constructing high-performance catalysts towards the hydrogen evolution of AB but also prompts the utilization of g-C3N4 in energy fields.


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