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Highly Dispersed Mo2C Anchored on N,P-Codoped Graphene as Efficient Electrocatalyst for Hydrogen Evolution Reaction

机译:高度分散的MO2C锚定,如N,P型石墨烯为氢进化反应的有效电催化剂

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摘要

Uniformly dispersed Mo2C were anchored on N, P-codoped graphene (Mo2C-N,P-rGO) by a facile method, during which phytic acid was employed as cross-linker to bridge the polyethyleneimine (PEI) modified graphene oxide (PEI-GO) and Mo ions through electrostatic adsorption and coordination bonding. Thanks to this ingenious strategy, the aggregation of Mo2C that usually occurs at high calcination temperature was effectively suppressed. This well-defined nanohybrid exhibits an excellent activity and high stability in hydrogen evolution reactions both in acidic and basic media due to the synergistic effects of the heteroatoms doped, accessibility of active sites, and conductivity of the two-dimensional (2D) structure. The obtained Mo2C-N,P-rGO requires only small overpotentials of 71 and 95 mV to drive 10 mAcm(-2) in alkaline and acidic solution, respectively. Benefiting from the protective effect of the coated carbon layers on the Mo2C surface, no obvious degradation was detected after 20 h of operation. This facile strategy may provide new opportunities for the precise design of functional 2D materials with unique properties.
机译:均匀分散的MO 2C通过容易方法在N,P型石墨烯(MO2C-N,P-RGO)上锚定,在此期间使用植酸作为交联剂以桥接聚乙烯亚胺(PEI)改性的石墨烯氧化物(PEI-GO )通过静电吸附和配位键合Mo离子。由于这种巧妙的策略,有效地抑制了通常发生在高煅烧温度下的MO2C的聚集。由于杂原子掺杂,活性位点的可行性和二维(2D)结构的电导率,这种定义的纳米冬次含量在酸性和碱性介质中表现出优异的活性和高稳定性。所得MO2C-N,P-RGO仅需要71和95mV的小型过电位,以分别在碱性和酸性溶液中驱动10mcm(-2)。受益于涂层碳层对Mo2C表面上的保护作用,在20小时后未检测到明显的降解。这种便利策略可以为具有独特性质的功能2D材料的精确设计提供新的机会。

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