材料科学
渗氮
电催化剂
兴奋剂
钌
纳米颗粒
催化作用
三聚氰胺
分解水
氢
纳米技术
化学工程
无机化学
光电子学
电极
电化学
物理化学
复合材料
图层(电子)
有机化学
化学
工程类
光催化
作者
Jitendra N. Tiwari,Ahmad M. Harzandi,Miran Ha,Siraj Sultan,Chang Woo Myung,Hyo Ju Park,Dong Yeon Kim,Pandiarajan Thangavel,Aditya Narayan Singh,Pankaj Sharma,S. Selva Chandrasekaran,Foad Salehnia,Ji‐Wook Jang,Hyeon Suk Shin,Zonghoon Lee,Kwang S. Kim
标识
DOI:10.1002/aenm.201900931
摘要
Abstract The most efficient electrocatalyst for the hydrogen evolution reaction (HER) is a Pt‐based catalyst, but its high cost and nonperfect efficiency hinder wide‐ranging industrial/technological applications. Here, an electrocatalyst of both ruthenium (Ru) single atoms (SAs) and N‐doped‐graphitic(G N )‐shell‐covered nitrided‐Ru nanoparticles (NPs) (having a Ru‐N x shell) embedded on melamine‐derived G N matrix { 1 : [Ru(SA)+Ru(NP)@RuN x @G N ]/G N }, which exhibits superior HER activity in both acidic and basic media, is presented. In 0.5 m H 2 SO 4 /1 m KOH solutions, 1 shows diminutive “negative overpotentials” (−η = |η| = 10/7 mV at 10 mA cm −2 , lowest ever) and high exchange current densities (4.70/1.96 mA cm −2 ). The remarkable HER performance is attributed to the near‐zero free energies for hydrogen adsorption/desorption on Ru(SAs) and the increased conductivity of melamine‐derived G N sheets by the presence of nitrided‐Ru(NPs). The nitridation process forming nitrided‐Ru(NPs), which are imperfectly covered by a G N shell, allows superb long‐term operation durability. The catalyst splits water into molecular oxygen and hydrogen at 1.50/1.40 V (in 0.1 m HClO 4 /1 m KOH), demonstrating its potential as a ready‐to‐use, highly effective energy device for industrial applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI