| Literature DB >> 29211437 |
Kewei Liu, Changlin Zhang1, Yuandong Sun, Guanghui Zhang2, Xiaochen Shen, Feng Zou, Haichang Zhang, Zhenwei Wu2, Evan C Wegener2, Clinton J Taubert, Jeffrey T Miller2, Zhenmeng Peng, Yu Zhu.
Abstract
Oxygen evolution reaction (OER) is a pivotal process in many energy conversion and storage techniques, such as water splitting, regenerative fuel cells, and rechargeable metal-air batteries. The synthesis of stable, efficient, non-noble metal-based electrocatalysts for OER has been a long-standing challenge. In this work, a facile and scalable method to synthesize hollow and conductive iron-cobalt phosphide (Fe-Co-P) alloy nanostructures using an Fe-Co metal organic complex as a precursor is described. The Fe-Co-P alloy exhibits excellent OER activity with a specific current density of 10 mA/cm2 being achieved at an overpotential as low as 252 mV. The current density at 1.5 V (vs reversible hydrogen electrode) of the Fe-Co-P catalyst is 30.7 mA/cm2, which is more than 3 orders of magnitude greater than that obtained with state-of-the-art Fe-Co oxide catalysts. Our mechanistic experiments and theoretical analysis suggest that the electrochemical-induced high-valent iron stabilizes the cobalt in a low-valent state, leading to the simultaneous enhancement of activity and stability of the OER catalyst.Entities:
Keywords: EXAFS; Fe−Co−P alloy; XANES; hollow sphere; oxygen evolution reaction; self-assembly
Year: 2017 PMID: 29211437 DOI: 10.1021/acsnano.7b04646
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881