脱氢
联氨(抗抑郁剂)
锐钛矿
催化作用
无定形固体
纳米颗粒
选择性
质子交换膜燃料电池
材料科学
化学工程
贵金属
解吸
化学
无机化学
纳米技术
有机化学
吸附
光催化
色谱法
工程类
作者
Xiaoya Liu,Ying Liu,Jingchao Wang,Jinghuan Ma
标识
DOI:10.1021/acs.iecr.1c03398
摘要
A safe, efficient, and responsive online hydrogen source is critical for the commercial application of proton exchange membrane fuel cells (PEMFCs). Catalysts play an important role in accelerating the development of hydrous hydrazine as a promising online hydrogen source, and the development of hydrous hydrazine (N2H4·H2O) as a promising online hydrogen source for PEMFCs requires superior catalysts with low cost and high activity. Herein, we report the synthesis of a supported amorphous catalyst NiMo/TiO2 using a combination of impregnation and coreduction methods. The NiMo/TiO2 catalyst can be responsive and completely decompose hydrous hydrazine to produce hydrogen in 1.5 min with a H2 selectivity of 100% and a turnover frequency (TOF) value of 484 h–1 under alkaline conditions at 343 K, outperforming most non-noble metal catalysts. Moreover, H2 selectivity has no decline after 10 cycles. The excellent catalytic properties can be attributed to the strong synergistic interaction between the support TiO2 and NiMo nanoparticles, as well as the amorphous NiMo nanoparticles possessing a high concentration of coordinated unsaturated sites. In addition, the doping of Mo leads to the modification of the electronic and geometric structures of the NiMo/TiO2 surface, which results in an easier cleavage of the N–H bond and desorption of reaction intermediates.
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