超高効率・高耐久な水分解用触媒:ニッケル-鉄合金被覆カーボンナノチューブ上への超微細ルテニウムナノ粒子触媒サイトの埋め込み
Qianqian Li1, Chengye Tu2, Fangzhi Huang3
1Anhui Provincial Key Laboratory of Green Carbon Chemistry, School of Chemistry and Material Engineering, Fuyang Normal University, Fuyang 236037, PR China.
Abstract:
The rational design of high-efficiency, low-loading Ru-based heterogeneous catalysts represents a promising strategy for advancing hydrogen production via electrochemical water splitting. Herein, a heterogeneous electrocatalyst was constructed through in situ reduction of ultra-small Ru nanoparticles on the surface of Ni3Fe alloy-encapsulated, N-doped carbon nanotubes (Ni3Fe/N-CNTs) derived from a NiFe-layered double hydroxide (LDH) precursor. The as-synthesized Ru-Ni3Fe/N-CNT catalyst exhibits exceptional activity and stability for the hydrogen evolution reaction (HER), requiring only an overpotential of 25 mV and a Tafel slope of 28.1 mV dec-1 at 10 mA cm-2. Furthermore, it maintains stable performance for over 100 h at 50 mA cm-2 without obvious activity attenuation. This outstanding performance is attributed to the strong electronic coupling between the Ru nanoparticles, the Ni3Fe alloy, and the N-CNT support, which collectively optimizes the reaction pathway and enhances structural stability. Additionally, the assembled Ru-Ni3Fe/N-CNT//Ni3Fe/N-CNT cell requires only1.58 V to achieve 20 mA cm-2 for overall water splitting. Comprehensive structural characterization, surface property and theoretical calculations collectively reveal that the inner Ni3Fe alloy and outer Ru induce charge redistribution, superhydrophilicity and electron coupling that not only optimizing the adsorption energy of H intermediates (ΔGH) but also facilitating the H2 desorption that can effectively improve the HER performance. The effective synergy between intrinsic electronic modulation and extrinsic nano structural engineering demonstrated in this study provides a viable avenue for the development of high-performance and cost-effective HER electrocatalysts.
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