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Ambient Electrosynthesis of Ammonia on a Biomass-Derived Nitrogen-Doped Porous Carbon Electrocatalyst: Contribution of Pyridinic Nitrogen AITranslate

China|University of Science and Technology of China; China|University of Science and Technology of China; Institute of Solid State Physics; Institute of Solid State Physics; China|University of Science and Technology of China; China|University of Science and Technology of China; Institute of Solid State Physics; Institute of Solid State Physics; Institute of Solid State Physics; Griffith University
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Publisher: ACS
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Abstract AITranslate

Here we report that alfalfa-derived nitrogen-doped porous carbon (NPC) fabricated by a pyrolysis method is electrochemically active for the N2 reduction reaction (NRR) at ambient conditions. The results demonstrate that the obtained NPC material with a nitrogen content of 6.35 atom % at 500 °C (NPC-500) exhibits high NRR activity with an NH3 yield rate of 1.31 mmol h–1 g–1cat. and a Faradaic efficiency of 9.98% at −0.4 V (vs RHE) in 0.005 M H2SO4 solution. The isotopic labeling experimental results using 15N2 feed gas and 15NPC-500 reveal that the yielded NH3 indeed resulted from the NPC-500 catalyzed NRR, and the doped pyridinic-N also contributes NH3 formation during NRR. The experimental and theoretical calculations results indicate that the doped pyridinic-N in the NPC catalyst during NRR can break away from its surface to form N vacancies in a carbon matrix as the catalytic active sites for N2 adsorption and activation.

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DOI:https://doi.org/10.1021/acsenergylett.8b02138

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Here we report that alfalfa-derived nitrogen-doped porous carbon (NPC) fabricated by a pyrolysis method is electrochemically active for the N2 reduction reaction (NRR) at ambient conditions. The results demonstrate that the obtained NPC material with a nitrogen content of 6.35 atom % at 500 °C (NPC-500) exhibits high NRR activity with an NH3 yield rate of 1.31 mmol h–1 g–1cat. and a Faradaic efficiency of 9.98% at −0.4 V (vs RHE) in 0.005 M H2SO4 solution. The isotopic labeling experimental results using 15N2 feed gas and 15NPC-500 reveal that the yielded NH3 indeed resulted from the NPC-500 catalyzed NRR, and the doped pyridinic-N also contributes NH3 formation during NRR. The experimental and theoretical calculations results indicate that the doped pyridinic-N in the NPC catalyst during NRR can break away from its surface to form N vacancies in a carbon matrix as the catalytic active sites for N2 adsorption and activation.

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GB/T 7714-2015 [1] Cuijiao Zhao, Shengbo Zhang, Miaomiao Han, et al. ACS Energy Letters, 2019(4). DOI:10.1021/acsenergylett.8b02138.
MLA [1] Cuijiao Zhao, et al., ACS Energy Letters, no. 4, 2019, https://doi.org/10.1021/acsenergylett.8b02138.
APA [1] Cuijiao Zhao, Shengbo Zhang, Miaomiao Han, Xian Zhang, Yanyan Liu, Wenyi Li, Chun Chen, Guozhong Wang, Haimin Zhang, & Huijun Zhao. (2019). ACS Energy Letters(4). https://doi.org/10.1021/acsenergylett.8b02138
IEEE [1] Cuijiao Zhao, Shengbo Zhang, Miaomiao Han, Xian Zhang, Yanyan Liu, Wenyi Li, Chun Chen, Guozhong Wang, Haimin Zhang, and Huijun Zhao, ACS Energy Letters, no. 4, 2019, doi: 10.1021/acsenergylett.8b02138.