Guanosine-assisted synthesis of a core-shell Mo2N/Mo2C/C structure for enhanced hydrogen evolution reaction

被引:3
作者
Xia, Miao [1 ,2 ]
Li, Shuchun [1 ]
Zhang, Xuefei [1 ]
Xie, Zailai [1 ]
机构
[1] Fujian Prov Univ, Fuzhou Univ, Key Lab Adv Carbon Based Funct Mat, Fuzhou 350016, Fujian, Peoples R China
[2] Changzhou Ctr Dis Control & Prevent, Changzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
DOPED CARBON; MOLYBDENUM SULFIDE; ELECTROCATALYSTS; NANOSHEETS; CATALYSTS;
D O I
10.1039/d3qi01420g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Coupling molybdenum-based materials with carbon is an effective strategy to improve the hydrogen evolution reaction (HER) performance. However, achieving the desired surface-active sites by regulating the catalyst's morphology presents a challenge. Here, we present a novel approach using guanosine as an assisting agent to synthesize core-shell Mo2N/Mo2C/C composites. By utilizing guanosine in combination with ammonium heptamolybdate, we induce the formation of new hierarchical Mo-based structures through intrinsic self-regulating mechanisms. The presence of rich interactions between guanosine molecules, such as hydrogen bonding and pi-pi stacking, plays a pivotal role in achieving this successful outcome. Notably, a core-shell spherical MoO2/CN polymer was formed when using an optimal amount of guanosine. By pyrolysis at 800 degrees C, this was transformed into the core-shell Mo2N/Mo2C/C composite. The unexpected core-shell structure was elucidated through ex situ XRD and SEM characterization, highlighting the dominance of carbon in the outer shells and molybdenum-rich phases in the core. The synthesized Mo2N/Mo2C/C composites exhibit a low overpotential of only 79 mV under alkaline conditions, which is comparable to that of commercially available Pt/C catalysts. Our study offers a promising route for developing noble-metal-free catalysts with enhanced HER performance, contributing to the advancement of green hydrogen generation technologies.
引用
收藏
页码:7018 / 7027
页数:10
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