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二维夹层结构介孔 MoC/碳/石墨烯纳米杂化材料用于高效析氢电催化剂。

Two-Dimensional Sandwich-Structured Mesoporous MoC/Carbon/Graphene Nanohybrids for Efficient Hydrogen Production Electrocatalysts.

机构信息

School of Chemistry and Chemical Engineering, School of Electronic Information and Electrical Engineering, Shanghai Key Laboratory of Electrical Insulation and Thermal Ageing , Shanghai Jiao Tong University , 800 Dongchuan Road , Shanghai 200240 , China.

Department of Chemistry and Food Chemistry , Technische Universität Dresden , Mommsenstrasse 4 , 01062 Dresden , Germany.

出版信息

ACS Appl Mater Interfaces. 2018 Nov 28;10(47):40800-40807. doi: 10.1021/acsami.8b15250. Epub 2018 Nov 14.

Abstract

The main challenge in water electrolysis, an appealing technique to alleviate future energy crisis, is the design of efficient electrocatalysts for hydrogen evolution reaction (HER). On the basis of an interface self-assembly approach, we synthesize mesoporous nitrogen-doped carbon/MoC/reduced graphene oxide nanohybrids (denoted as mNC-MoC@rGO), which represent a new type of two-dimensional MoC/carbon hybrid nanomaterials and possess a sandwichlike structure with well-defined mesopores. The method involves the co-self-assembly of spherical micelles formed from polystyrene- block-poly(ethylene oxide), pyrrole (Py) monomers, and molybdate ions (MoO) on GO surfaces in aqueous solution, followed by polymerization of Py and calcination of the nanocomposites at 900 °C under nitrogen atmosphere. The resultant mNC-MoC@rGO nanosheets possess high N contents, large specific surface areas (SSAs), and 4 nm MoC particles well-distributed in the mesoporous carbon matrix. The MoC content is controllable in the range of 18.4-42.4 wt % by adjusting the feed amount of MoO. In particular, mNC-MoC@rGO with an SSA of 344 m/g and a MoC content of ca. 28 wt % exhibits the highest HER catalytic activity in 1 M KOH electrolyte, with a 95 mV overpotential at 10 mA/cm, a Tafel slope of 49.8 mV/dec, and a long-term stability of 60 h at 20 mA/cm. This study blazes a trail for the synthesis of new functional nanomaterials with potential applications as efficient HER electrocatalysts.

摘要

在缓解未来能源危机的有吸引力的技术中,水分解面临的主要挑战是设计用于析氢反应 (HER) 的高效电催化剂。基于界面自组装方法,我们合成了介孔氮掺杂碳/碳化钼/还原氧化石墨烯纳米杂化物 (表示为 mNC-MoC@rGO),这代表了一种新型二维碳化钼/碳混合纳米材料,具有明确的介孔的三明治结构。该方法涉及在水溶液中在 GO 表面上共自组装由聚苯乙烯-嵌段-聚氧化乙烯、吡咯 (Py) 单体和钼酸盐离子 (MoO) 形成的球形胶束,然后聚合 Py 并在氮气气氛下于 900°C 下煅烧纳米复合材料。所得的 mNC-MoC@rGO 纳米片具有高 N 含量、大比表面积 (SSA) 和 4nm MoC 颗粒在介孔碳基质中均匀分布。通过调整 MoO 的进料量,可以将 MoC 含量控制在 18.4-42.4wt% 的范围内。特别是,具有 344 m/g 的 SSA 和约 28wt%的 MoC 含量的 mNC-MoC@rGO 在 1M KOH 电解质中表现出最高的 HER 催化活性,在 10mA/cm 时具有 95mV 的过电位、49.8mV/dec 的塔菲尔斜率和 20mA/cm 时 60h 的长期稳定性。该研究为合成具有作为高效 HER 电催化剂应用潜力的新型功能纳米材料开辟了道路。

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