铱
化学
催化作用
电解水
析氧
密度泛函理论
本体电解
电解
无机化学
多金属氧酸盐
纳米颗粒
协同催化
化学工程
质子交换膜燃料电池
联轴节(管道)
电化学
氧气
膜
光化学
分解水
质子
电催化剂
多相催化
反应中间体
氢键
甲烷氧化偶联
作者
Xueru Zhao,Tianyou Mou,Jesse Long,Arephin Islam,Sinwoo Kang,Nancy N. Kariuki,Deborah J. Myers,Ping Liu,José A. Rodríguez,Jingguang G. Chen,Kotaro Sasaki
摘要
High Resolution Image Download MS PowerPoint Slide Supporting iridium (Ir)-based materials on stable and suitable substrates is an efficient strategy to improve their catalytic performance for the oxygen evolution reaction (OER) in harsh acidic environments. Herein, we report a series of Ir catalysts supported on boron–carbon-nitride (BCN), denoted as Ir/BCN. Detailed experiments combined with density functional theory calculations demonstrate strong interactions between Ir nanoparticles (NPs) and the BCN support, significantly contributing to the improved OER performance. Among the synthesized catalysts, the Ir/BCN-75 catalyst outperforms commercial Ir black and IrO 2 in both half-cell and proton exchange membrane water electrolysis (PEMWE) tests. Specially, the Ir/BCN-75 catalyst achieves a high current density of 2.94 A cm –2 at 1.9 V with a low Ir loading of 0.26 mg cm –2 in PEMWE measurements, exceeding most Ir-based catalysts reported to date. The BCN support interacts strongly with Ir, wherein Ir–N bonding directs the Ir NP growth and enhances electrocatalytic activity, while Ir–B bonding contributes to the stability of the Ir/BCN catalyst.
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