分解水
杂原子
反应性(心理学)
电化学
催化作用
材料科学
电解水
兴奋剂
三聚氰胺
化学工程
碳纤维
石墨烯
热解
电解
纳米技术
化学
电极
光催化
电解质
有机化学
替代医学
戒指(化学)
复合材料
物理化学
病理
工程类
复合数
医学
光电子学
作者
Pengfei Guo,Guangrui Liu,Jie Yin,Hongxin Hu,Enze Li,Yating Meng,Hongjin Gao,Wenpin Wang,Zhongcheng Li
出处
期刊:Fuel
[Elsevier BV]
日期:2023-08-19
卷期号:355: 129476-129476
被引量:8
标识
DOI:10.1016/j.fuel.2023.129476
摘要
Catalytic water splitting into H2 is a prospective way to alleviate the fossil fuels crisis. To date, α-MoO3 nanostructures show the low activity in water electrolysis reaction because of their poor conductive ability. The rational design of α-MoO3 with tunable electron structure is greatly desired to promote electrocatalytic performance. Herein, we utilize a facile one-pot method to prepare MoO3/N, P co-doped carbon sheets (MoO3/NPC). Carbon sheets are regulated by N and P doping, which are generated by thermal pyrolysis of melamine phosphate. Accordingly, the partial reduction of MoO3 nanosheets is elaborated by coordinative unsaturated Mo5+ sites. Experimental investigations show that MoO3 nanosheets are anchored on N and P co-doped carbon sheets. The electrochemical studies indicate that MoO3/NPC presents excellent water oxidation reactivity with 231 mV@10 mA/cm2, which is superior to RuO2 (283 mV). In comparison to α-MoO3 nanosheets (204 mV), the enhanced water reduction reactivity is achieved on MoO3/NPC with 144 mV at 10 mA/cm2. Serving as the bi-functional catalysts to drive water splitting, MoO3/NPC exhibits a low voltage of 1.59 V at 10 mA/cm2. Our work highlights that heteroatom engineering could mediate the electron state of MoO3 and thereby accelerate water splitting rate.
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