过电位
催化作用
密度泛函理论
化学
合金
选择性
物理化学
氮气
无机化学
化学工程
材料科学
计算化学
电化学
有机化学
电极
工程类
作者
Yifan Yu,Wei Zhang,Fu-li Sun,Qiaojun Fang,Jin-kong Pan,Wen‐Xian Chen,Gui‐Lin Zhuang
标识
DOI:10.1016/j.mcat.2022.112141
摘要
To search excellent catalyst for electrocatalytic nitrogen reduction reaction (eNRR) is of great importance for the alternative to the traditional Haber-Bosch process. Herein, based on density functional theory (DFT) calculations, we systematically investigated the catalytic mechanism of eNRR on different-proportions high-entropy alloy (HEA) FeCoNiCuPd. The calculation of formation energy shown the dependence of structural stability on the ratio of constituents. Meanwhile, it is found that Ni0.3(FeCoCuPd)0.175 features high thermal stability. The Ni0.3(FeCoCuPd)0.175 with exposed crystal plane (111) exhibited excellent performance of eNRR with the lowest overpotential of 0.34 eV. Catalytically kinetic results demonstrated that Ni0.3(FeCoCuPd)0.175 follows the distal reaction pathway and the rate-determining step (RDS) was found to be *N2 →*NNH with the barrier of 0.50 eV. Relative to the secondary reaction of hydrogen evolution reaction (HER), such catalyst achieves the excellent selectivity of 99%. Detailed electronical calculations results indicated the connection between catalytic activity and d-band center, shedding light on the critical role of Ni element ratio in the catalytic performance.
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