过电位
磷化物
密度泛函理论
钌
化学工程
氢
吸附
材料科学
分解水
无机化学
催化作用
化学
金属有机骨架
物理化学
计算化学
有机化学
电化学
电极
工程类
光催化
作者
Jiahuan Luo,Jing Wang,Yao Guo,Jiawei Zhu,Huihui Jin,Zhiwei Zhang,Dao‐Jun Zhang,Yongsheng Niu,Shaogang Hou,Jimin Du,Daping He,Yuli Xiong,Lei Chen,Shichun Mu,Yunhui Huang
标识
DOI:10.1016/j.apcatb.2021.121043
摘要
Hydrogen generation from electrical water splitting has become a greatly increasing requirement for energy systems, however, highly effective and durable electrocatalysts towards universal-pH hydrogen evolution reaction (HER) remain a big challenge. Herein, we design and synthesize ruthenium di-phosphide (RuP2) confined in carbon layers (RuP2-C) with a unique yolk-shell structure (RuP2[email protected]2-C) from MOF. As expected, it not only exceeds the HER activity of Pt catalysts, with very tiny overpotentials at 10 mA cm−2 (9 and 17 mV in 1.0 M KOH and 0.5 M H2SO4, individually), but also has high stability. Besides, it also exhibits a low overpotential (40 mV) close to Pt catalysts and high stability in 1.0 M PBS, indicating that RuP2[email protected]2-C ([email protected]) owns outstanding HER performance at all pH values. Density functional theory (DFT) calculation results further unravel that the P-site on the surface of [email protected] possesses low hydrogen adsorption energy, beneficial for boosting the HER activity.
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