journal article·2020-08-24

Phase-Dependent Reactivity of Nickel Molybdates for Electrocatalytic Urea Oxidation

Kailong Hu, Samuel Jeong, Ganesan Elumalai, Suresh Kukunuri, Jun-ichi Fujita, Yoshikazu Ito

ACS Applied Energy Materials· Volume 3· Issue 8
Publisher page

Abstract

Identifying the influence of the phase of a catalyst on its reactivity is crucial for guiding the rational design of highly active electrocatalysts. Herein, we unveil the phase-dependent reactivity of nickel molybdates (NiMoO4) for the electrocatalytic urea oxidation reaction (UOR). Various NiMoO4 phases, namely, α-NiMoO4, β-NiMoO4, and the hydrate NiMoO4·xH2O, were synthesized, and their structural characteristics and electrochemical properties were related to their electrocatalytic performance for the UOR. The NiMoO4 phase was found to determine its reactivity, and phase-dependent UOR activities were observed. In particular, β-NiMoO4 exhibited a higher activity and faster kinetics than NiMoO4·xH2O and α-NiMoO4, which was attributed to the large electrochemical surface area, low Tafel slope, and small charge–transfer resistance of β-NiMoO4. Moreover, hydrogen generation via β-NiMoO4-catalyzed urea electrolysis achieved a much lower cell voltage (1.498 V to reach 10 mA cm–2) than that required for water electrolysis (1.633 V to reach 10 mA cm–2). This work provides insights into design strategies for high-activity electrocatalysts for energy-efficient hydrogen production.
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Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Advanced Photocatalysis Techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Institute of Applied Physics, Graduate School of Pure and Applied Sciences, University of Tsukuba, Tsukuba 305-8573, Japan

PRESTO, Japan Science and Technology Agency, Saitama 332-0012, Japan

Funding

Ministry of Education, Culture, Sports, Science and Technology · Precursory Research for Embryonic Science and Technology · Japan Society for the Promotion of Science

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