Affiliation:
1. Department of Nano Convergence Engineering (BK21 Four) Jeonbuk National University Jeonju Jeonbuk 54896 Republic of Korea
2. Department of Chemistry Tribhuvan University Amrit Campus Kathmandu 44613 Nepal
3. Division of Science Education Graduate School of Department of Energy Storage/Conversion Engineering Jeonbuk National University Jeonju Jeonbuk 54896 Republic of Korea
4. Carbon Composite Research Centre Department of Polymer‐Nano Science and Technology Jeonbuk National University Jeonju Jeonbuk 54896 Republic of Korea
Abstract
AbstractRational design of highly efficient noble‐metal‐unbound electrodes for hydrogen and oxygen production at increased current density is crucial for robust water‐splitting. A facile hydrothermal and room‐temperature aging method is presented, followed by chemical vapor deposition (CVD), to create a self‐sacrificed hybrid heterostructure electrocatalyst. This hybrid material, (Mn−(Co,Ni)2P/CoP/(N,S)−C), comprises manganese‐doped cobalt nickel phosphide (Mn−(Co,Ni)2P) nanofeathers and cobalt phosphide (CoP) nanocubes embedded in a nitrogen and sulfur co‐doped carbon matrix (N,S)−C on nickel foam. The catalyst exhibits excellent performance in both the hydrogen evolution reaction (HER; η10 = 61 mV) and oxygen evolution reaction (OER; η10 = 213 mV) due to abundant active sites, high porosity, and enhanced hetero‐interface interaction between Mn−(Co2P−Ni2P) CoP, and (N,S)−C supported by significant synergistic effects observed among different phases through density functional theory (DFT) calculations. Impressively, (Mn−(Co,Ni)2P/CoP/(N,S)−C (+,−) shows an extra low cell voltage of 1.49 V@10 mA cm−2. Moreover, the catalyst exhibits remarkable stability at 100 and 300 mA cm−2 when operating as a single stack cell electrolyzer. The superior electrochemical activity is attributed to the enhanced electrode–electrolyte interface among the multiple phases of the hybrid structure.
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry
Cited by
8 articles.
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