N-Doped Nanoporous Carbon Scaffold As an Electrocatalyst for CO2 Reduction

The rising level of CO 2 in the atmosphere poses a major threat to our global climate [1]. Renewable energy are promising alternatives but the utilization of renewable energy is challenging because of its intermittency. The key solution is to develop an energy storage system that can store energy and then release it as needed. CO 2 reduction reaction (CO 2 RR) uses abundant CO 2 present in the atmosphere and renewable energy as the input power. Therefore, increasing interest has been focused on electrochemical routes to transform CO 2 into useful products. However, the reduction of CO 2 is thermodynamically and kinetically unfavorable. To overcome the energy barrier of CO 2 RR, the development of high efficiency and high selectivity catalysts is a key goal of CO 2 RR research. Metallic catalysts have attracted much attention for CO 2 RR and have achieved some successes. However, most metallic catalysts exhibit large CO 2 RR overpotentials and insufficient selectivity. Also, the high price of noble metals is a key obstacle to scale-up and commercialization of these materials for CO 2 RR. Carbon is a very promising candidate to advance CO 2 RR due to its high specific surface areas and good conductivity. However, carbon atoms are electrically neutral and therefore it is difficult to activate the CO 2 molecules and adsorb the intermediate. Therefore, it is necessary to develop novel carbon catalysts to enhance their catalytic activity for CO 2 RR. Nitrogen is the most commonly used carbon doping atom due to its high electronegativity, which leads to polarization of the adjacent carbon atoms, thus enhancing the electronic/ionic conductivity [2]. Many carbon materials, such as carbon nanotubes and graphene, have been doped with N and investigated as CO 2 RR catalysts [3][4], with some N-doped materials exhibiting a 85% Faradaic efficiency towards CO production[5]. In this work, a nitrogen-doped templated nanoporous carbon scaffold (N-doped NCS) was investigated as a catalyst material for electrochemical CO 2 reduction. The NCS is a novel, templated, binder-free, self-supported, fully tunable mesoporous carbon material[6] that gives a high active site density and good conductivity. NCS material, having a pore size of either 12, 50 or 85 nm, was heated in NH 3 gas at 700 °C for 7 hours to prepare N-doped NCS. SEM and TEM were used to confirm the NCS morphology, while XPS, EDX and elemental analysis were used to determine the N content of the NCS material. The electrochemical performance of the N-doped NCS was carried out first using CV in CO 2 sat. 0.1 M KHCO 3 in a glass cell. After that, a membrane electrode assembly (MEA) CO 2 electrolyzer was used to determine the CO 2 reduction activity. An N-doped NCS (IrO 2 -coated) was used as the anode and an anion exchange membrane (AEM) was used as the separator during CO 2 electrolysis, with humidified CO 2 gas used at the cathode side. The gas products were collected from the cathode outlet and injected into a gas chromatography system for analysis. No liquid products were observed in the solution that was released to the cell outlet. The performance of N-doped NCS will be presented based on the results obtained in various solution-flow cell configurations. Effect of N-doped NCS preparation optimization will also be discussed. Based on both the CV results and the MEA CO 2 electrolyzer data, the onset potential of CO 2 RR was comparable to what has been reported by others for N-doped carbons, but the high internal surface area of the NCS, combined with its high extent of N doping, may give the N-doped NCS some advantages. A maximum 90% FE CO was achieved and the stability of the catalytic material was also studied in the flow cell systems. References [1] C. Costentin, M. Robert, and J.-M. Savéant, “Catalysis of the electrochemical reduction of carbon dioxide,” Chem. Soc. Rev. , 2013. [2] T. Zheng, K. Jiang, and H. Wang, “Recent Advances in Electrochemical CO 2 -to-CO Conversion on Heterogeneous Catalysts,” Adv. Mater. , vol. 30, no. 48, p. 1802066, Nov. 2018. [3] X. Wang et al. , “Emerging Nanostructured Carbon-based Non-precious Metal Electrocatalysts for Selectively Electrochemical CO 2 Reduction to CO,” J. Mater. Chem. A , 2019. [4] H. Cui, Y. Guo, L. Guo, L. Wang, Z. Zhou, and Z. Peng, “Heteroatom-doped carbon materials and their composites as electrocatalysts for CO 2 reduction,” J. Mater. Chem. A , vol. 6, no. 39, pp. 18782–18793, 2018. [5] T. Ma et al. , “Heterogeneous electrochemical CO 2 reduction using nonmetallic carbon-based catalysts: current status and future challenges,” Nanotechnology , vol. 28, no. 47, p. 472001, Nov. 2017. [6] Birss, Viola, L. I. Xiaoan, and Dustin Banham. "Porous carbon films." U.S. Patent Application No. 15/124,847.