Boosting Electrocatalytic Urea Production via Promoting Asymmetric C-N Coupling

被引:46
|
作者
Qiu, Mengyi [1 ]
Zhu, Xiaorong [2 ]
Bo, Shuowen [3 ]
Cheng, Kai [4 ]
He, Nihan [1 ]
Gu, Kaizhi [5 ]
Song, Dezhong [1 ]
Chen, Chen [1 ]
Wei, Xiaoxiao [1 ]
Wang, Dongdong [1 ]
Liu, Yingying [1 ]
Li, Shuang [1 ]
Tu, Xiaojin [1 ]
Li, Yafei [2 ]
Liu, Qinghua [3 ]
Li, Conggang [4 ]
Wang, Shuangyin [1 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Peoples R China
[2] Nanjing Normal Univ, Coll Chem & Mat Sci, Nanjing 210023, Peoples R China
[3] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230022, Peoples R China
[4] Chinese Acad Sci, State Key Lab Magnet Resonance & Atom & Mol Phys, Natl Ctr Magnet Resonance Wuhan Collaborat Innovat, Key Lab Magnet Resonance Biol Syst,Wuhan Inst Phys, Wuhan 430064, Peoples R China
[5] Cent South Univ, Inst Adv Study, Changsha 410083, Peoples R China
来源
CCS CHEMISTRY | 2023年 / 5卷 / 11期
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
asymmetric coupling; C-N bond; urea syn-thesis; electrocatalysis; active site; ENERGY-TRANSFER; AMMONIA; REDUCTION; MECHANISM; FTIR;
D O I
10.31635/ccschem.023.202202408
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrocatalytic C-N coupling shows great potential in direct and sustainable urea synthesis. However, the mechanism of interaction between catalytic sites and intermediate species is currently unclear, and explor-ing corresponding strategies to boost urea synthesis is urgent. Herein, we demonstrated that a multihole structure could preserve the Cu+ component of Cu2O spheres under electrochemical reduction conditions. An in situ formed Cu0-Cu+ site thermodynamically and kinetically promoted the asymmetric coupling pro-cess of *CO and *NO, thereby boosting the urea pro-duction. The impressive urea yield rates of 29.2 and 114.0 mmol h-1 g-1 were realized for electrochemical coupling of CO2 with nitrate and nitrite, respectively. The multihole-Cu2O exhibits both superior activity and long-term stability compared to the electrocata-lysts with a reconstructed Cu0-dominated surface. This work provides insights into the identification and design of the active site for C-N coupling and urea synthesis.
引用
收藏
页码:2617 / 2627
页数:11
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