磷化物
钌
纳米颗粒
碳纤维
催化作用
氮气
电催化剂
氢
金属
无机化学
化学
磷
材料科学
化学工程
纳米技术
电化学
有机化学
物理化学
电极
复合数
工程类
复合材料
作者
Qian Luo,Caili Xu,Qian Chen,Jie Wu,Yi Wang,Yun Zhang,Guangyin Fan
标识
DOI:10.1016/j.ijhydene.2019.08.028
摘要
Pt-group metal phosphides are widely utilized as efficient electrocatalysts for hydrogen evolution reaction (HER), whereas most of the synthetic strategies are complicated, dangerous, and toxic with the use of large amount of nitrogen (N) and/or phosphorus (P) sources. Here, we report the synthesis of ruthenium phosphide nanoparticles (NPs) confined into N/P dual-doped carbon by pyrolyzing self-prepared ruthenium-organophosphine complex using 1,3,5-triaza-7-phosphadamantane (PTA) as the ligand and N/P sources. The achieved S–RuP2/NPC displayed excellent electrocatalytic activity (overpotentials of 19, 37, and 49 mV in alkaline, neutral, and acidic media, respectively, at 10 mA cm−2) toward HER at all pH ranges. The high performance of S–RuP2/NPC must be ascribed to the homogeneously distributed and P-rich RuP2 NPs with the diameter of 3.29 nm on the NPC surface, which can considerably improve the atom utilization for HER. The present synthetic strategy not only avoids the use of additional N/P sources but also the generation of flammable and toxic PH3 gas. This synthetic strategy can be extended to prepare other traditional metal phosphides for electrocatalytic applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI