Tailoring the Electronic Structure of Co2P by N Doping for Boosting Hydrogen Evolution Reaction at All pH Values

• Published in: ACS catalysis Vol. 9; no. 4; pp. 3744 - 3752
• Main Authors: Men, Yana, Li, Peng, Zhou, Juanhua, Cheng, Gongzhen, Chen, Shengli, Luo, Wei
• Format: Journal Article
• Language: English
• Published: American Chemical Society 05.04.2019
• Subjects: reaction kinetics; DFT; pH-universal; transition metal phosphide; hydrogen evolution reaction
• ISSN: 2155-5435; 2155-5435
• DOI: 10.1021/acscatal.9b00407

The development of precious-metal-free electrocatalysts with high-efficiency for hydrogen evolution reaction (HER) at all pHs is of great interest for the development of electrochemical overall splitting technologies. Despite that intense efforts have been made to developing cost-effective electrocatalysts toward HER under both acidic and alkaline electrolytes with high efficiency, electrocatalysts with remarkable performance in neutral media are rare. Herein, N atoms doped Co2P nanorod arrays grown on carbon cloth (N–Co2P/CC) have been successfully synthesized and further used as efficient electrocatalysts for HER at all pH values. Specially, the N–Co2P/CC exhibits an overpotential of 42 mV at the current density of 10 mA cm –2 with long-term stability in 1.0 M PBS (phosphate-buffered solution), which is comparable to the benchmark Pt/CC. Density functional theory (DFT) calculations suggest nitrogen doping could tailor the electronic structure of Co2P, leading to optimized adsorption free energies of water (ΔG *H2O) and hydrogen (ΔG *H), facilitating hydrogen generation through the Volmer–Heyrovsky mechanism.