4.8 Article

Unveiling the Optimal Interfacial Synergy of Plasma-Modulated Trimetallic Mn-Ni-Co Phosphides: Tailoring Deposition Ratio for Complementary Water Splitting

Journal

ENERGY & ENVIRONMENTAL MATERIALS
Volume 6, Issue 2, Pages -

Publisher

WILEY
DOI: 10.1002/eem2.12324

Keywords

DFT; overall water splitting; oxygen evolution reaction (OER); hydrogen evolution reaction (HER); plasma; ternary metallic phosphides (MnNiCo)

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This study demonstrates an innovative approach to synthesize flower-like trimetallic Mn, Ni, Co phosphide catalysts. The catalysts show outstanding catalytic performance for both HER and OER, as well as excellent durability.
Designing highly active, durable, and nonprecious metal-based bifunctional electrocatalysts for overall water electrolysis is of urgent scientific importance to realize the sustainable hydrogen production, which remains a grand challenge. Herein, an innovative approach is demonstrated to synthesize flower-like 3D homogenous trimetallic Mn, Ni, Co phosphide catalysts directly on nickel foam via electrodeposition followed by plasma phosphidation. The electrochemical activity of the catalysts with varying Mn:Ni:Co ratios is assessed to identify the optimal composition, demonstrating that the equimolar trimetallic phosphide yields an outstanding HER catalytic performance with a current density of 10 mA cm(-2) at an ultra-low overpotential of similar to 14 mV, outperforming the best reported electrocatalysts. This is asserted by the DFT calculations, revealing strong interaction of the metals and the P atom, resulting in enhanced water activation and optimized G(H)* values for the HER process. Moreover, this optimal composition appreciably catalyzes the OER by exposing more intrinsic active species in-situ formed on the catalyst surface during the OER. Therefore, the Mn-1-Ni-1-Co-1-P-(O)/NF catalyst exhibits a decreased overpotential of similar to 289 mV at 10 mA cm(-2). More importantly, the electrocatalyst sustains perfect durability up to 48 h at a current density of 10 mA cm(-2) and continued 5000 cycling stability for both HER and OER. Meanwhile, the assembled MNC-P/NF parallel to MNC-P/NF full water electrolyzer system attains an extremely low cell voltage of 1.48 V at 10 mA cm(-2). Significantly, the robust stability of the overall system results in a remarkable current retention of similar to 96% after a continuous 50-h run. Therefore, this study provides a facile design and a scalable construction of superb bifunctional ternary MNC-phosphide electrocatalysts for efficient electrochemical energy production systems.

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