分解水
催化作用
双功能
材料科学
电化学
氮气
石墨烯
无机化学
化学工程
电催化剂
纳米复合材料
兴奋剂
电解质
光催化
纳米技术
电极
化学
物理化学
光电子学
有机化学
工程类
作者
Binbin Jiang,Tao Wang,Yafei Cheng,Fan Liao,Konglin Wu,Mingwang Shao
标识
DOI:10.1021/acsami.8b11970
摘要
Nitrogen-doped graphene (NG) chemically coupled with graphitic carbon nitride (g-C3N4) may facilitate the kinetics of overall electrochemical water splitting. Herein, a facile strategy is adopted to synthesize monodispersed Ir nanoparticles on g-C3N4/NG layers. Benefiting from the synergistic effect between different components of the catalyst, the optimal Ir/g-C3N4/NG catalyst with a low content of Ir (5.9 wt %) exhibits highly active for electrochemical water splitting in acidic electrolyte. Specifically, as a hydrogen evolution reaction catalyst, the optimal Ir/g-C3N4/NG exhibits a Tafel slope of 22 mV·dec-1. The optimal catalyst requires an overpotential of 22 mV to reach the current density of 10 mA·cm-2, the value of which is superior to Ir/NG (32 mV) and 20 wt % Pt/C (28 mV) catalysts; as an oxygen evolution reaction catalyst, it also achieve the Tafel slope of only 72.8 mV·dec-1. At the overpotential of 300 mV, the mass activity of the optimal Ir/g-C3N4/NG catalyst is 2.8 times as large as that of 5.7 wt % Ir/NG catalyst. More significantly, as a bifunctional catalyst, the optimal Ir/g-C3N4/NG achieves a current density of 10 mA·cm-2 with a potential of only 1.56 V and displays good stability for overall water splitting. This work provides a new strategy to design highly efficient acidic catalysts for electrochemical overall water splitting.
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