Cobalt/Molybdenum Phosphide and Oxide Heterostructures Encapsulated in N-Doped Carbon Nanocomposite for Overall Water Splitting in Alkaline Media
Source abstract
Abstract
The development of designing and searching inexpensive electrocatalysts with high activity for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is significant to enable water splitting as a future renewable energy source. Herein, we synthesize a new CoP(MoP)-CoMoO3 heterostructure coated by a N-doped carbon shell [CoP(MoP)-CoMoO3@CN] via thermal decomposition and phosphatizing of the CoMoO4·0.9H2O nanowires encapsulated in N-doped carbon. At 10 mA·cm–2, this CoP(MoP)-CoMoO3@CN nanocomposite exhibits superior electrocatalytic activity at low overpotentials of 296 mV for OER and 198 mV for HER in alkaline media. More importantly, we achieve a current density of 10 mA·cm–2 at 1.55 V by using this CoP(MoP)-CoMoO3@CN as both cathode and anode for overall water splitting. This promising performance could be due to the high activity of CoP(MoP)-CoMoO3 and the good conductivity of the external mesoporous N-carbon shell, which makes the CoP(MoP)-CoMoO3@CN nanowires a competitive alternative to noble-metal-based catalysts for water splitting.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Fuel Cells and Related Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Heavy Oil Processing, College of Chemical Engineering, China University of Petroleum Beijing, Beijing 102249, China
Funding
Ministry of Education of the People's Republic of China · Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology · Science Foundation of China University of Petroleum, Beijing
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