材料科学
钴
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
工程类
冶金
物理
光学
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]
日期:2023-09-13
卷期号:117: 108901-108901
被引量:30
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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