Ray Chaiti, Dutta Soumen, Sahoo Ramkrishna, Roy Anindita, Negishi Yuichi, Pal Tarasankar
Department of Chemistry, Indian Institute of Technology, Kharagpur, India.
Department of Applied Chemistry, Tokyo University of Science, Tokyo, 1628601, Japan.
Chem Asian J. 2016 May 20;11(10):1588-96. doi: 10.1002/asia.201600173. Epub 2016 Apr 23.
Inspired by the attractive catalytic properties of palladium and the inert nature of carbon supports in catalysis, a concise and simple methodology for in situ nitrogen-doped mesoporous-carbon-supported palladium nanoparticles (Pd/N-C) has been developed by carbonizing a palladium dimethylglyoximate complex. The as-synthesized Pd/N-C has been exfoliated as a fuel cell catalyst by studying the electro-oxidation of methanol and formic acid. The material synthesized at 400 °C,namely, Pd/N-C-400,exhibitssuperior mass activity and stability among catalysts synthesized under different carbonization temperaturesbetween300 and 500 °C. The unique 1D porous structure in Pd/N-C-400 helps better electron transport at the electrode surface, which eventually leads to about five times better catalytic activity and about two times higher stability than that of commercial Pd/C. Thus, our designed sacrificial metal-organic templatedirected pathway becomes a promising technique for Pd/N-C synthesis with superior catalytic performances.
受钯的诱人催化性能以及碳载体在催化中的惰性本质启发,通过碳化二甲基乙二肟钯配合物,已开发出一种简洁且简单的原位氮掺杂介孔碳负载钯纳米颗粒(Pd/N-C)的方法。通过研究甲醇和甲酸的电氧化,已将所合成的Pd/N-C剥离为燃料电池催化剂。在400°C下合成的材料,即Pd/N-C-400,在300至500°C不同碳化温度下合成的催化剂中表现出优异的质量活性和稳定性。Pd/N-C-400中独特的一维多孔结构有助于在电极表面实现更好的电子传输,最终导致其催化活性比商业Pd/C约高五倍,稳定性约高两倍。因此,我们设计的牺牲金属有机模板导向途径成为一种具有前景的合成具有优异催化性能的Pd/N-C的技术。