过电位
单斜晶系
法拉第效率
催化作用
四方晶系
氨
纳米颗粒
氧化还原
化学
电化学
化学工程
相(物质)
氨生产
材料科学
无机化学
纳米技术
晶体结构
物理化学
电极
结晶学
有机化学
工程类
作者
Xin Xue,Qiming Qu,Islam E. Khalil,Yuting Huang,Wei Mo,Jie Chen,Weina Zhang,Fengwei Huo,Wenjing Liu
标识
DOI:10.1016/j.cclet.2023.108654
摘要
Electrocatalytic nitrogen reduction reaction (NRR) is considered as an attractive approach for ammonia synthesis under mild conditions. A bottleneck of NRR is the exploration of efficient catalysts for accelerating reaction kinetics, among which heterogeneous structures possessing distinct atomic arrangement could modify electronic structure, and therefore altering their NRR activity. Here, we report a facile strategy for fabricating hetero-phase metal oxides derived from metal organic framework that are further integrated with Au nanoparticles as NRR catalysts. The phase composition of zirconia can be easily adjusted by simply changing the reaction temperature, where the monoclinic and tetragonal phases with the roughly close proportions have a distinct interface, leading to a strong interaction between Au and ZrO2. The enhanced interaction renders Au to be more electropositive and facilitates stronger binding to N2. As a result, a remarkable ammonia yield of 22.32 μg h−1 mgcat.−1 and a Faradaic efficiency of 31.92% can be achieved at low overpotential. This work is expected to pave the way for the design of heterogeneous structures and the exploration of hetero-phase nanostructures in boosting the electrocatalytic NRR.
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