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在具有高电催化析氢性能的多孔 N 掺杂碳基质中嵌入的结构明确的 MoC 纳米粒子。

Well-Defined MoC Nanoparticles Embedded in Porous N-Doped Carbon Matrix for Highly Efficient Electrocatalytic Hydrogen Evolution.

机构信息

National Institute for Advanced Materials, School of Materials Science and Engineering , Nankai University , Tianjin 300350 , China.

Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Collaborative Innovation Center of Chemical Science and Engineering (Tianjin) , Nankai University , Tianjin 300071 , China.

出版信息

ACS Appl Mater Interfaces. 2018 Oct 3;10(39):33276-33286. doi: 10.1021/acsami.8b12108. Epub 2018 Sep 18.

Abstract

On the design of efficient and affordable electrocatalysts for water reduction half reaction, this paper fabricates molybdenum carbide nanoparticles uniformly loaded in highly porous N-doped carbon matrix derived from polyaniline-molybdate monolith with the use of graphitic carbon nitride (g-CN) as template. The obtained molybdenum carbide-carbon hybrid catalysts (MoC@NCS) exhibit extraordinarily electrochemical hydrogen evolution activity with a small overpotential of 89 and 81 mV to deliver a current density of 10 mA cm in alkaline (1.0 M KOH) and acidic (0.5 M HSO) medium, respectively, even comparable to noble-metal Pt/C benchmark. Specially, MoC@NCS also shows excellent long-term durability in alkaline or acidic electrolyte. Furthermore, the obtained carbon matrix (NCS) featuring high content of N dopants and hierarchically porous architecture exhibits high catalytic efficiency for oxygen evolution reaction in alkaline electrolyte. For a further step, the obtained NCS coupled with the MoC@NCS, working as anodic and cathodic electrodes, in a two-electrode alkaline electrolyzer for overall water splitting, which can obtain a current density of 10 mA cm at 1.69 V, along with robust operation durability. The synergistic effect of the porous carbon matrix of high nitrogen content and the molybdenum carbide nanoparticles of uniform distribution, together with hierarchically porous structure, should be responsible for the outstanding electrocatalytic HER performance. This work presents an easy and cost-effective strategy to prepare molybdenum-based materials with controlled size for electrocatalytic hydrogen evolution.

摘要

在设计高效且经济的水电解还原半反应电催化剂方面,本文使用石墨相氮化碳 (g-CN) 作为模板,通过将苯胺-钼酸盐单体原位聚合转化为聚吡咯-钼酸盐介孔块体,然后碳化制备出均匀负载在高度多孔 N 掺杂碳基质中的碳化钼纳米粒子。所得的碳化钼-碳杂化催化剂 (MoC@NCS) 在碱性 (1.0 M KOH) 和酸性 (0.5 M HSO) 介质中分别具有 89 和 81 mV 的小过电势即可达到 10 mA cm 的电流密度,表现出非凡的电化学析氢活性,甚至可与贵金属 Pt/C 基准相媲美。特别地,MoC@NCS 在碱性或酸性电解质中也表现出优异的长期耐久性。此外,所获得的具有高 N 掺杂含量和分级多孔结构的碳基质 (NCS) 在碱性电解质中对析氧反应表现出高催化效率。更进一步,将获得的 NCS 与 MoC@NCS 结合,作为阳极和阴极电极,在碱性两电极电解槽中用于全水分解,可在 1.69 V 时获得 10 mA cm 的电流密度,同时具有稳健的操作耐久性。高氮含量多孔碳基质与均匀分布的碳化钼纳米粒子以及分级多孔结构的协同效应,应该是其具有出色电催化 HER 性能的原因。这项工作提出了一种简便且经济高效的策略,用于制备具有可控尺寸的钼基材料,用于电催化析氢。

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