Interfacial Engineering of MoO2 -FeP Heterojunction for Highly Efficient Hydrogen Evolution Coupled with Biomass Electrooxidation

Adv Mater. 2020 Apr;32(17):e2000455. doi: 10.1002/adma.202000455. Epub 2020 Mar 16.

Abstract

Simultaneous highly efficient production of hydrogen and conversion of biomass into value-added products is meaningful but challenging. Herein, a porous nanospindle composed of carbon-encapsulated MoO2 -FeP heterojunction (MoO2 -FeP@C) is proposed as a robust bifunctional electrocatalyst for hydrogen evolution reaction (HER) and biomass electrooxidation reaction (BEOR). X-ray photoelectron spectroscopy analysis and theoretical calculations confirm the electron transfer from MoO2 to FeP at the interfaces, where electron accumulation on FeP favors the optimization of H2 O and H* absorption energies for HER, whereas hole accumulation on MoO2 is responsible for improving the BEOR activity. Thanks to its interfacial electronic structure, MoO2 -FeP@C exhibits excellent HER activity with an overpotential of 103 mV at 10 mA cm-2 and a Tafel slope of 48 mV dec-1 . Meanwhile, when 5-hydroxymethylfurfural is chosen as the biomass for BEOR, the conversion is almost 100%, and 2,5-furandicarboxylic acid (FDCA) is obtained with the selectivity of 98.6%. The electrolyzer employing MoO2 -FeP@C for cathodic H2 and anodic FDCA production requires only a low voltage of 1.486 V at 10 mA cm-2 and can be powered by a solar cell (output voltage: 1.45 V). Additionally, other BEORs coupled with HER catalyzed by MoO2 -FeP@C also have excellent catalytic performance, implying their good versatility.

Keywords: biomass electrooxidation; electron transfer; heterojunctions; hydrogen evolution; porous nanospindles.