Electron-deficient cobalt nanocrystals for promoted nitrate electrocatalytic reduction to synthesize ammonia

材料科学 拉曼光谱 纳米晶 吡啶 X射线光电子能谱 吸附 金属 无机化学 化学工程 纳米技术 化学 物理化学 有机化学 物理 工程类 光学 冶金
作者
Baopeng Yang,Yulong Zhou,Zhencong Huang,Binbao Mei,Qing Kang,Gen Chen,Xiaohe Liu,Zheng Jiang,Min Liu,Ning Zhang
出处
期刊:Nano Energy [Elsevier BV]
卷期号:117: 108901-108901 被引量:87
标识
DOI:10.1016/j.nanoen.2023.108901
摘要

The Co-based electrocatalysts are promising for NO3− reduction reactions to synthesize NH3. However, NH3 yielding efficiencies over oxidation state Co compounds and electron-rich Co metal are still low due to the difficulties in simultaneously satisfying both NO3− adsorption and NHx hydrogenation. Herein, an electron-deficient Co nanocrystals is designed by interacting Co with pyridine nitrogen to promote the electrocatalytic NO3− reductions to synthesize NH3. Theoretical calculations predict that pyridine nitrogen modifications induce the electron-deficiency in Co nanoparticles, facilitating both the NO3− adsorption and energy-barrier decrease of *NH to *NH2. A pyridine nitrogen-doped carbon modified Co nanocrystals (Co/PN-C) are thus fabricated. The X-ray photoelectron and absorption near-edge spectroscopies confirm the electron-deficient state of Co metal in as prepared Co/PN-C materials. The Co/PN-C exhibits a high Faraday efficiency of 97.8 ± 2.0% toward NH3 generation, a remarkable NO3− removal efficiency of approximate 100%, and an outstanding NH3 yield rate of 109 mg h−1 cm−2 with a current density of 1.3 A cm−2. These performances are significantly higher than mostly reported Co-based electrocatalysts. In-situ Raman and Fourier-transform infrared spectra further confirm that Co/PN-C promotes NO3− adsorption and *NH hydrogenation to form NH3. This work gives effective strategy to tune electron-deficient Co nanocrystals for promoted NO3− electrocatalytic reduction to synthesize NH3.
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