纳米片
Atom(片上系统)
催化作用
尿素
漫反射红外傅里叶变换
电化学
空位缺陷
化学
氢原子
纳米技术
材料科学
无机化学
结晶学
物理化学
有机化学
电极
光催化
计算机科学
嵌入式系统
烷基
作者
Lu Pan,Jingnan Wang,Fei Lu,Qiang Liu,Yuhang Gao,Yan‐Feng Wang,Jingzhe Jiang,Chao Sun,Jian Wang,Xi Wang
标识
DOI:10.1002/anie.202216835
摘要
As rising star materials, single-atom and dual-atom catalysts have been widely reported in the electro-catalysis area. To answer the key question: single-atom and dual-atom catalysts, which is better for electrocatalytic urea synthesis? we design two types of catalysts via a vacancy-anchorage strategy: single-atom Pd1 -TiO2 and dual-atom Pd1 Cu1 -TiO2 nanosheets. An ultrahigh urea activity of 166.67 molurea molPd-1 h1 with the corresponding 22.54 % Faradaic efficiency at -0.5 V vs. reversible hydrogen electrode (RHE) is achieved over Pd1 Cu1 -TiO2 , which is much higher than that of Pd1 -TiO2 . Various characterization including an in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and theoretical calculations demonstrate that dual-atom Pd1 Cu1 site in Pd1 Cu1 -TiO2 is more favorable for producing urea, which experiences a C-N coupling pathway with a lower energy barrier compared with Pd1 in Pd1 -TiO2 .
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