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磷化钴纳米颗粒对析氢反应的高活性电催化作用。

Highly active electrocatalysis of the hydrogen evolution reaction by cobalt phosphide nanoparticles.

机构信息

Department of Chemistry and Materials Research Institute, The Pennsylvania State University, University Park, PA 16802 (USA).

出版信息

Angew Chem Int Ed Engl. 2014 May 19;53(21):5427-30. doi: 10.1002/anie.201402646. Epub 2014 Apr 11.

DOI:10.1002/anie.201402646
PMID:24729482
Abstract

Nanoparticles of cobalt phosphide, CoP, have been prepared and evaluated as electrocatalysts for the hydrogen evolution reaction (HER) under strongly acidic conditions (0.50 M H2SO4, pH 0.3). Uniform, multi-faceted CoP nanoparticles were synthesized by reacting Co nanoparticles with trioctylphosphine. Electrodes comprised of CoP nanoparticles on a Ti support (2 mg cm(-2) mass loading) produced a cathodic current density of 20 mA cm(-2) at an overpotential of -85 mV. The CoP/Ti electrodes were stable over 24 h of sustained hydrogen production in 0.50 M H2SO4. The activity was essentially unchanged after 400 cyclic voltammetric sweeps, suggesting long-term viability under operating conditions. CoP is therefore amongst the most active, acid-stable, earth-abundant HER electrocatalysts reported to date.

摘要

磷化钴纳米粒子(CoP)已被制备并评估为在强酸条件下(0.50 M H2SO4,pH 0.3)用于析氢反应(HER)的电催化剂。通过使 Co 纳米粒子与三辛基膦反应,合成了均匀的、多面的 CoP 纳米粒子。CoP 纳米粒子负载在 Ti 载体上的电极(2 mg cm(-2) 的质量负载)在过电势为-85 mV 时产生 20 mA cm(-2) 的阴极电流密度。在 0.50 M H2SO4 中持续生产氢气 24 小时后,CoP/Ti 电极稳定。经过 400 次循环伏安扫描后,活性基本不变,表明在工作条件下具有长期可行性。因此,CoP 是迄今为止报道的最活跃、耐酸、丰富的 HER 电催化剂之一。

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