二硫化钼
材料科学
催化作用
化学工程
过电位
纳米复合材料
碳纤维
电催化剂
分解水
电解质
纳米线
纳米技术
电极
电化学
化学
复合材料
有机化学
复合数
工程类
物理化学
光催化
作者
Mengting Chen,Aiqing Zhong,Weipeng Liu,Chen Shi,Yingju Liu
标识
DOI:10.1016/j.ijhydene.2020.07.238
摘要
The design and synthesis of non-precious metal catalysts that effectively convert water into molecular hydrogen in an acidic environment is essential to reduce the energy loss in the water splitting process. Among them, molybdenum disulfide (MoS2) is considered as an effective alternative to Pt-based materials due to its excellent structure properties. Here, by using metal-organic framework (MOF) as the precursor, sodium molybdate as molybdenum sources and thiourea as sulfur sources, a hollow structure of Co–MoS2 electrocatalyst was prepared on highly conductive carbon nanowire arrays/carbon cloth (CA/CC) by hydrothermal reaction. The combination of carbon nanowire arrays and carbon cloth ensures the high conductivity, while the hollow Co–MoS2 structure promotes the penetration of electrolytes and the release of hydrogen bubbles. The overpotential is only 296 mV when the current density was ~1500 mA/cm2, which shows excellent catalytic hydrogen evolution activity of the material. In addition, the three-dimensional hollow structure avoids the use of adhesives between the active material and the self-supporting material, which can improve the stability of the material and provides a new idea to design commercial electrocatalysts.
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