电合成
材料科学
催化作用
法拉第效率
尿素
氢
产量(工程)
串联
制氢
可逆氢电极
无机化学
化学工程
电化学
分解水
电催化剂
原位
析氧
联轴节(管道)
氨生产
氧化还原
电极
作者
Yan Wang,Shuai Xia,Jianfang Zhang,Cuiping Yu,Jiayu Liu,Miao Han,Kui Chen,Hao Tan,Hao Tan,Yong Zhang,Hark Hoe Tan,Hark Hoe Tan,Yucheng Wu
标识
DOI:10.1002/adfm.202519152
摘要
Abstract Electrochemical urea synthesis is critically restricted by insufficient supply of active hydrogen ( * H) for the hydrogeneration of CO 2 and nitrate (NO 3 − ). Here, a tandem sites catalyst is designed by anchoring Cu clusters on MoS 2 /MoO 2 nanosheets (Cu‐MoS 2 /MoO 2 ), with the Cu sites activating CO 2 and NO 3 − and the Mo sites dissociating water to produce * H. In situ spectroscopic analysis and theoretical calculations reveal that the sufficient * H supply greatly promotes intermediate hydrogenation, thus enhancing C─N coupling for urea synthesis. Consequently, the Cu‐MoS 2 /MoO 2 catalyst displays significantly enhance performance of urea synthesis from CO 2 and NO 3 − , achieving a high yield of 117.5 mmol h −1 g cat. −1 at −0.6 V versus the reversible hydrogen electrode (RHE). Besides, stable electrocatalytic urea production is maintained for 68 h without a decline in yield or Faradaic efficiency. This work provides a meaningful perspective on modulating active hydrogen to promote urea production.
科研通智能强力驱动
Strongly Powered by AbleSci AI