Ir/g-C3N4/Nitrogen-Doped Graphene Nanocomposites as Bifunctional Electrocatalysts for Overall Water Splitting in Acidic Electrolytes

被引:101
作者
Jiang, Binbin [1 ,2 ]
Wang, Tao [1 ]
Cheng, Yafei [2 ]
Liao, Fan [2 ]
Wu, Konglin [3 ]
Shao, Mingwang [2 ]
机构
[1] Anqing Normal Univ, Sch Chem & Chem Engn, Prov Key Lab Funct Coordinat Cpds & Nanomat, Anqing 246001, Peoples R China
[2] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou 215123, Peoples R China
[3] Anhui Normal Univ, Anhui Key Lab Funct Mol Solids,Ctr Single Atom Cl, Minist Educ,Coll Chem & Mat Sci,Key Lab Funct Mol, Anhui Lab Mol Based Mat,State Key Lab Cultivat Ba, Wuhu 241002, Peoples R China
基金
中国国家自然科学基金;
关键词
Ir; g-C3N4; NG; water splitting; acidic electrolyte; NITROGEN-DOPED GRAPHENE; GRAPHITIC CARBON NITRIDE; HYDROGEN EVOLUTION; OXYGEN EVOLUTION; PHOTOCATALYTIC PERFORMANCE; IRIDIUM NANOPARTICLES; HIGHLY EFFICIENT; FACILE SYNTHESIS; CATALYST; OXIDE;
D O I
10.1021/acsami.8b11970
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
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.
引用
收藏
页码:39161 / 39167
页数:7
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