论文标题

并行的电催化氮固定在异互际边界之外

Parallelising Electrocatalytic Nitrogen Fixation Beyond Heterointerfacial Boundary

论文作者

An, Tae-Yong, Je, Minyeong, Roh, Seung Hun, Surendran, Subramani, Han, Mi-Kyung, Lim, Jaehyoung, Lee, Dong-Kyu, Janani, Gnanaprakasam, Choi, Heechae, Kim, Jung Kyu, Sim, Uk

论文摘要

氮(N2)还原反应(NRR)是Haber-Bosch工艺的环保替代品,可生产具有高可持续性的氨(NH3)。然而,多步进途径中的上坡能量的显着幅度是其串行反应的瓶颈。在此,提出了平行反应的概念,以使用多相氧化二硝酸盐(V2O3/VN)混合系统通过NRR积极促进NH3的产生。密度功能理论计算表明,V2O3/VN连接通过交换中间N2H4*和NH2*产品与NRR途径平行,以避免向最终NH3生成的大量上坡能量。这种交换是由这两个物种覆盖率差异所驱动的。 V2O3/VN连接的反应并行策略对多步氮还原的影响通过氨的产量率提高18.36 micro Mol H^-1 cm^-2-2,而Faraday效率(Fe)为26.62%,为26.62%,在-0.3 v v v v v us a f us a feus a feus a 16. f e Electolode in 0.1 moh eletter the 0.1 m a squos of then fe at 0.1 m a selope and oferogen fe at 0.1 m a squos oferogen of the 0.1 m a。分别是单相V2O3和VN的6.22倍。因此,将多相氧化物/氮化物引入基于过渡金属的电催化剂可能是实现N2固定方法的一种有前途的方法。

The nitrogen (N2) reduction reaction (NRR) is an eco-friendly alternative to the Haber-Bosch process to produce ammonia (NH3) with high sustainability. However, the significant magnitude of uphill energies in the multi-step NRR pathways is a bottleneck of its serial reactions. Herein, the concept of a parallelized reaction is proposed to actively promote NH3 production via the NRR using a multi-phase vanadium oxide-nitride (V2O3/VN) hybrid system. Density functional theory calculations revealed that the V2O3/VN junction parallelizes NRR pathways by exchanging intermediate N2H4* and NH2* products to avoid massive uphill energies towards final NH3 generation. Such an exchange is driven by the difference in coverage of the two species. The impact of the reaction parallelization strategy for multi-step nitrogen reduction is demonstrated with the V2O3/VN junction by an increased ammonia yield rate of 18.36 micro mol h^-1 cm^-2 and a Faraday efficiency (FE) of 26.62% at -0.3 V versus a reversible hydrogen electrode in a 0.1 M aqueous KOH electrolyte, of which FE value exhibits 16.95 times and 6.22 times higher than that of single-phase V2O3 and VN, respectively. The introduction of multi-phase oxides/nitrides into a transition metal-based electrocatalyst can thus be a promising approach to realizing an alternative method for N2 fixation.

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