Hetero-Interface Manipulation in MoOx@Ru to Evoke Industrial Hydrogen Production Performance with Current Density of 4000 mA cm-2

被引:25
|
作者
Zhang, Yu [1 ,2 ]
Ma, Chaoqun [3 ,4 ,5 ]
Zhu, Xiaojuan [1 ,2 ]
Qu, Kaiyu [1 ,2 ]
Shi, Peidong [1 ,2 ]
Song, Leyang [1 ,2 ]
Wang, Jing [1 ,2 ]
Lu, Qipeng [3 ,4 ,5 ]
Wang, An-Liang [1 ,2 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, Key Lab Colloid & Interface Chem, Minist Educ, Jinan 250100, Shandong, Peoples R China
[2] Shandong Univ, Suzhou Res Inst, Suzhou 215123, Jiangsu, Peoples R China
[3] Univ Sci & Technol Beijing, Sch Mat Sci & Engn, 30 Xueyuan Rd, Beijing 100083, Peoples R China
[4] Zhongguancun Inst Human Settlements Engn & Mat, Beijing 100083, Peoples R China
[5] Univ Sci & Technol Beijing, Shunde Innovat Sch, Foshan 528399, Peoples R China
基金
中国国家自然科学基金;
关键词
anion exchange membrane waters electrolyzer; hetero-interface manipulation; hydrogen evolution reaction; large current densities; EVOLUTION ACTIVITY; CATALYST;
D O I
10.1002/aenm.202301492
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Constructing and manipulating hetero-interfaces for the electrocatalytic hydrogen evolution reaction (HER) is highly desirable, but still poses a significant challenge. Herein, this work adopts a facile way to controllably synthesize three different hetero-interfaces by anchoring ultrafine Ru nanoparticles on various MoOx nanotube (NT) substrates, including MoO2, MoO2/MoO3, and MoO3. Remarkably, MoO2@Ru NT displays excellent HER activity with tiny overpotentials of 89 and 131 mV delivering large current densities of 500 and 1000 mA cm(-2), respectively, far surpassing two other hetero-interfaces, commercial Ru/C, Pt/C catalysts. Impressively, this hetero-interface even achieves an exceptionally large current density of 4000 mA cm(-2) at an overpotential of 322 mV. Moreover, MoO2@Ru NT presents exceptional stability for at least 100 h at 1000 mA cm(-2) with negligible degradation. Both experimental observations and theoretical calculations suggest that moderate electron transfer from Ru to MoO2 enhances the water dissociation kinetics, and optimizes the hydrogen adsorption/desorption, thus simultaneously speeding up the HER kinetics. Furthermore, an anion exchange membrane electrolyzer assembled by obtained MoO2@Ru NT as a cathode electrocatalyst, shows attractive activity and excellent durability, with a low voltage of 1.78 V at 1000 mA cm(-2), and a prolonged time period for 200 h at 1000 mA cm(-2).
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页数:10
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