Department of Chemistry and Chemical Biology, Cornell University , Ithaca, New York 14850, United States.
ACS Nano. 2014 Jun 24;8(6):6106-13. doi: 10.1021/nn5014337. Epub 2014 May 21.
We report a robust noncarbon Ti0.5Cr0.5N support synthesized by an efficient solid-solid phase separation method. This ternary nitride exhibits highly porous, sintered, and random network structure with a crystallite size of 20-40 nm, resulting in a high specific surface area. It is not only kinetically stable in both acid and alkaline media, but also electrochemically stable in the potential range of fuel cell operation. Two typical anode reactions, formic acid oxidation in acid media and methanol oxidation in alkaline media, are employed to investigate the possibility of Ti0.5Cr0.5N as an alternative to carbon. Bimetallic PdAg nanoparticles (∼4 nm) act as anode catalysts for the two anode reactions. PdAg/Ti0.5Cr0.5N exhibits much higher mass activity and durability for the two reactions than PdAg/C and Pd/C catalyst, suggesting that mesoporous Ti0.5Cr0.5N is a very promising support in both acid and alkaline media.
我们报道了一种通过高效的固-固相分离方法合成的稳健的非碳 Ti0.5Cr0.5N 载体。这种三元氮化物具有高度多孔、烧结和随机网络结构,晶粒尺寸为 20-40nm,比表面积高。它不仅在酸和碱性介质中动力学稳定,而且在燃料电池操作的电位范围内电化学稳定。两种典型的阳极反应,即酸性介质中的甲酸氧化和碱性介质中的甲醇氧化,被用来研究 Ti0.5Cr0.5N 作为碳替代物的可能性。双金属 PdAg 纳米颗粒(约 4nm)作为两种阳极反应的阳极催化剂。与 PdAg/C 和 Pd/C 催化剂相比,PdAg/Ti0.5Cr0.5N 对两种反应表现出更高的质量活性和耐久性,这表明介孔 Ti0.5Cr0.5N 在酸性和碱性介质中都是一种很有前途的载体。