Liu Yingjie, Wu Zhaohui, Bai Sha, Shen Tianyang, Li Qian, Liu Guihao, Sun Xiaoliang, Hu Yihang, Song Ziheng, Chu Jinfeng, Song Yu-Fei
State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology Beijing 100029 P. R. China
Quzhou Institute for Innovation in Resource Chemical Engineering Quzhou 324000 Zhejiang Province P. R. China.
Nanoscale Adv. 2024 Mar 18;6(9):2363-2370. doi: 10.1039/d4na00167b. eCollection 2024 Apr 30.
Herein, we report the successful fabrication of a series of transition metal doped Ni nanoparticles (NPs) coordinated with Ni single atoms in nitrogen-doped carbon nanotubes (denoted as NiM-NCNTs, M = Mn, Fe, Co, Cu and Zn; Ni = Ni single atom). X-ray absorption fine structure reveals the coexistence of Ni single atoms with Ni-N coordination and NiM NPs. When applied for electrocatalytic CORR, the NiM-NCNT compounds show the Faradaic efficiency of CO (FE) with a volcano-like tendency of Mn < Fe ≈ Co < Zn < Cu, in which the NiCu-NCNT exhibits the highest FE of 96.92%, a current density of 171.25 mA cm and a sustainable stability over 24 hours at a current density of 100 mA cm, outperforming most reported examples in the literature. Detailed experiments and theoretical calculations reveal that for NiCu-NCNTs, the electron transfer from NiCu NPs to Ni single atoms strengthens the adsorption of *COOH intermediates. Moreover, the d-band center of Ni-N in NiCu-NCNT is upshifted, providing stronger binding with the reaction intermediates of *COOH, whereas the NiCu NPs increase the Gibbs free energy change of the Volmer step, suppressing the competitive HER.
在此,我们报道了一系列过渡金属掺杂的镍纳米颗粒(NPs)与氮掺杂碳纳米管中的镍单原子配位成功制备(表示为NiM-NCNTs,M = Mn、Fe、Co、Cu和Zn;Ni = 镍单原子)。X射线吸收精细结构揭示了镍单原子与Ni-N配位和NiM NPs共存。当应用于电催化CO还原反应(CORR)时,NiM-NCNT化合物显示出CO的法拉第效率(FE)呈现出类似火山的趋势,即Mn < Fe ≈ Co < Zn < Cu,其中NiCu-NCNT表现出最高的FE为96.92%,电流密度为171.25 mA cm²,并且在100 mA cm²的电流密度下可持续稳定超过24小时,优于文献中报道的大多数实例。详细的实验和理论计算表明,对于NiCu-NCNTs,电子从NiCu NPs转移到镍单原子增强了COOH中间体的吸附。此外,NiCu-NCNT中Ni-N的d带中心上移,与COOH的反应中间体提供更强的结合,而NiCu NPs增加了Volmer步骤的吉布斯自由能变化,抑制了竞争性析氢反应(HER)。