A Universal Approach for Sustainable Urea Synthesis via Intermediate Assembly at the Electrode/Electrolyte Interface

Author:

Tu Xiaojin1,Zhu Xiaorong2,Bo Shuowen3,Zhang Xiaoran1,Miao Ruping14,Wen Guobin1,Chen Chen1,Li Jing5,Zhou Yangyang1,Liu Qinghua3,Chen Dawei14,Shao Huaiyu5,Yan Dafeng6,Li Yafei7,Jia Jianfeng8,Wang Shuangyin1ORCID

Affiliation:

1. State Key Laboratory of Chem/Bio-Sensing and Chemometrics College of Chemistry and Chemical Engineering Hunan University Changsha Hunan China

2. School of Chemistry and Chemical Engineering Nantong University Nantong Jiangsu P. R. China

3. National Synchrotron Radiation Laboratory University of Science and Technology of China Hefei Anhui P. R. China

4. College of Material Science and Engineering Qingdao University of Science and Technology Qingdao Shandong P. R. China

5. Guangdong-Hong Kong-Macau Joint Laboratory for Photonic-Thermal-Electrical Energy Materials and Devices Institute of Applied Physics and Materials Engineering University of Macau, Avenida da Universidade Taipa, Macau SAR 999078 P. R. China

6. College of Chemistry and Chemical Engineering Hubei University Wuhan Hubei P. R. China

7. College of Chemistry and Materials Science Nanjing Normal University Nanjing Jiangsu P. R. China

8. Key Laboratory of Magnetic Molecules and Magnetic Information Materials (Ministry of Education) School of Chemistry and Material Science Shanxi Normal University Taiyuan Shanxi P. R. China

Abstract

AbstractElectrocatalytic C−N coupling process is indeed a sustainable alternative for direct urea synthesis and co‐upgrading of carbon dioxide and nitrate wastes. However, the main challenge lies in the unactivated C−N coupling process. Here, we proposed a strategy of intermediate assembly with alkali metal cations to activate C−N coupling at the electrode/electrolyte interface. Urea synthesis activity follows the trend of Li+<Na+<Cs+<K+. In the presence of K+, a world‐record performance was achieved with a urea yield rate of 212.8±10.6 mmol h−1 g−1 on a single‐atom Co supported TiO2 catalyst at −0.80 V versus reversible hydrogen electrode. Theoretical calculations and operando synchrotron‐radiation Fourier transform infrared measurements revealed that the energy barriers of C−N coupling were significantly decreased via K+ mediated intermediate assembly. By applying this strategy to various catalysts, we demonstrate that intermediate assembly at the electrode/electrolyte interface is a universal approach to boost sustainable urea synthesis.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Natural Science Foundation of Shandong Province

Publisher

Wiley

Subject

General Chemistry,Catalysis

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