Meera Sebastian, Subrata Das and Nishanth Karimbintherikkal Gopalan
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引用次数: 0
摘要
电催化 N2 固定为在环境条件下有效生产氨气提供了一种碳中和且节能的途径。然而,它在实现高产氨量和 FE 方面通常面临重大挑战。这是因为缺乏高效的电催化剂,无法轻松激活强 N2 三键并抑制竞争性 HER。金属氧化物被广泛认为是氮还原反应(NRR)的有效电催化剂,因为它们可以帮助轻松激活 N2 的三键。在此,我们证明了混合金属氧化物 Bi4Ti3O12 具有在环境条件下作为电催化氮还原反应催化剂的潜力,在 0.1 M HCl 中,当电压为 -0.6 V 时,氨产量为 27.8 μg h-1 mgcat-1,FE 为 22%。Ti 和 Bi 的 N2 结合能力、Bi 6p 带和 N 2p 轨道的强相互作用以及 Bi 的低氢吸附能共同抑制了 HER 的表面电子可及性,从而促进了 N2 的轻松活化,提高了 NRR 的电催化活性和选择性。
Electrosynthesis of NH3 from N2 using nanostructured Bi4Ti3O12 catalyst†
The electrocatalytic N2 fixation provides a carbon-neutral and energy-efficient pathway for producing ammonia effectively under ambient conditions. However, it typically faces significant challenges in achieving a high ammonia yield and FE. This is attributed to the lack of efficient electrocatalysts that can easily activate the strong N2 triple bond and suppress the competing HER. Metal oxides are widely acknowledged as effective electrocatalysts for nitrogen reduction reaction (NRR) because they can assist in easily activating the triple bond of N2. Herein, we demonstrate that a mixed metal oxide, Bi4Ti3O12, holds potential as a catalyst for electrocatalytic NRR under ambient conditions with an ammonia yield of 27.8 μg h−1 mgcat−1 and FE of 22% at −0.6 V in 0.1 M HCl. The synergistic effect of the N2 binding ability of Ti and Bi, coupled with a robust interaction of the Bi 6p band and N 2p orbitals and the low hydrogen adsorption energy of Bi collectively inhibit surface electron accessibility for the HER, thereby facilitating the easy activation of N2 and results in better electrocatalytic activity and selectivity for NRR.
期刊介绍:
Sustainable Energy & Fuels will publish research that contributes to the development of sustainable energy technologies with a particular emphasis on new and next-generation technologies.