Ru-Mo2C nanoclusters anchored on N, P crownshaft-derived porous carbon for efficient hydrogen evolution in alkaline seawater

被引:0
作者
Sam, Daniel Kobina [1 ,2 ,3 ,4 ]
Tang, Zhen [2 ,3 ,4 ]
Cao, Yan [1 ,2 ,3 ,4 ]
机构
[1] Univ Sci & Technol China, Sch Energy Sci & Engn, Hefei 230026, Peoples R China
[2] Chinese Acad Sci, Guangzhou Inst Energy Convers, Guangzhou 510640, Peoples R China
[3] CAS Key Lab Renewable Energy, Guangzhou 510640, Peoples R China
[4] Guangdong Prov Key Lab New & Renewable Energy Res, Guangzhou 510640, Peoples R China
基金
中国国家自然科学基金;
关键词
Porous carbon; Hydrogen evolution reaction; Seawater; Hydrogen spillover; CATALYTIC-ACTIVITY; DOPED CARBON; ELECTROCATALYSTS; NANOPARTICLES; MORPHOLOGY; OXIDE; MO2C; RU;
D O I
10.1016/j.jcis.2025.138213
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
Noble-metal-based electrocatalysts have long been the top choice for hydrogen evolution reaction (HER) electrocatalysts, offering low overpotentials and Tafel slopes. Nonetheless, their use in alkaline media has been limited due to the sluggish kinetics of the Volmer process. Herein, we develop a unique biomass-derived heteroatom-doped porous carbon material via self-templating to anchor ruthenium-molybdenum carbide (Ru-Mo2C) nanoclusters. The synthesized Ru-Mo2C-supported heteroatom-doped porous carbon (RuMo-NPCSPC) shows exceptional electrocatalytic ability for alkaline HER, achieving low overpotentials of 49, 85, and 92 mV to realize 10 mA cm-2 in 1 M KOH, alkaline seawater, and simulated alkaline seawater, respectively. The RuMo-NPCSPC also boasts low Tafel slopes and ultrahigh Faradaic Efficiencies (98-100 %) in alkaline media, outperforming most noble metal-based catalysts and mercantile Pt/C. Most importantly, the catalyst demonstrates outstanding stability, signifying its potential for industrial hydrogen production. This work delivers profound perspectives into synthesizing advanced nanostructured porous carbon materials using abundant biomass resources for alkaline HER.
引用
收藏
页数:14
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