光化学
氨
电子顺磁共振
分解
光催化
催化作用
化学
产量(工程)
水溶液
分子
反应机理
密度泛函理论
激进的
辐照
金属
反应中间体
材料科学
计算化学
物理化学
有机化学
核磁共振
核物理学
物理
冶金
作者
Arisa Utsunomiya,Atsushi Okemoto,Yukihiro Nishino,Kitagawa Kensuke,Hisayoshi Kobayashi,Keita Taniya,Yuichi Ichihashi,Satoru Nishiyama
标识
DOI:10.1016/j.apcatb.2017.01.045
摘要
Photodecomposition of NH3 to H2 and N2 was carried out using metal-supported TiO2 (M/TiO2) photocatalysts in an aqueous NH3 solution under UV irradiation at room temperature. Ni/TiO2 photocatalysts indicated the highest yield of H2. The NH2 radical was formed as a dominant intermediate during NH3 decomposition, as confirmed by electron spin resonance measurements. Reaction pathways via NH2 radical formation were also investigated in detail by density functional theory. The results showed that H2 and the H2N-NH2 as intermediate were formed by the coupling of an NH2 radical and an NH3 molecule in the gas phase during the photodecomposition of NH3. We believe that our findings would be useful for further developing efficient catalytic systems.
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