Enhanced Oxygen Evolution Activity and Stability of RuO2(110) Surface by Ti Doping

Abstract

Introduction Developing highly active and durable electrocatalysts for the oxygen evolution reaction (OER) is essential for efficient hydrogen production through polymer electrolyte membrane water electrolysis (PEMWE). Although RuO2 exhibits the highest OER activity among pure transition metal oxide catalysts, its low durability hampers its practical application as an OER catalyst for PEMWE. Recent studies have shown that the incorporation of dissimilar metal elements, such as Ni, Mn, and Cu, effectively enhances the OER activity and stability of RuO2 in acidic electrolytes (1-3). In this study, we focus on Ti, a corrosion-resistant element in the PEMWE environment, and investigate the effects of doping amounts on the OER activity and stability of a RuO2(110) single crystal model catalyst surface. Experimental Non-doped rutile-type TiO2(110) single crystals were used as sample substrates. Ru and Ti, with a total thickness of 40 nm, were deposited onto the substrate at 400 ℃ under 0.5 Pa-O2 partial pressure using the arc-plasma deposition (APD) method. Subsequently, the sample was post-annealed at 400℃ for 1 hour in air using a tube furnace. Hereafter, the samples are denoted as RuO2-Tix (x represents the atomic percentage of doped Ti).Oxygen evolution activity was measured by linear sweep voltammetry (LSV) at a scan rate of 20 mV s-1 in N2-purged 0.1 M HClO4 at room temperature. Chronopotentiometry (CP) was conducted at 1 mA cm-2 for 120 min to evaluate the durability. The electrochemical impedance spectroscopy was conducted at 1.6 V vs. reversible hydrogen electrode (RHE) to measure the solution resistance. All the LSV and CP data were iR-corrected using the Rs values. Out-of-plane X-ray diffraction (XRD) analysis was carried out to evaluate the crystal structure. The dissolution amounts of Ru into the electrolyte after CP were evaluated by inductively coupled plasma mass spectrometry (ICP-MS). Results and Discussions Fig. 1(a) presents the out-of-plane XRD patterns of Ti-doped and non-doped RuO2(110) samples. The results indicate that (110)-oriented Ti-doped and non-doped RuO2 thin films were successfully obtained on TiO2 substrates. However, the peak position of RuO2(110) gradually shifts to the lower angle side, and the peak becomes less distinct with increasing Ti-doping amounts, suggesting that doped Ti is dissolved in the RuO2 crystal lattice and the crystallinity decreases with increasing doping amounts. Initial LSV curves for OER are shown in Fig. 1(b). The current density of RuO2-Ti4, 5, and 7 samples significantly increases at higher potential regions above 1.6 V vs. RHE, while RuO2-Ti2 and 10 exhibit decreased activity. The CP curves presented in (c) demonstrate that Ti doping, especially at 5 and 7 at.%, effectively suppresses the overpotential increase during CP. The dissolution amounts of Ru after 120 min of CP are summarized in (d). The dissolution amounts tend to decrease with increasing Ti-doping amounts. These results clearly show that an appropriate amount of Ti-doping effectively enhances both the OER activity and electrochemical stability of the RuO2(110) surface.AcknowledgmentsThis study was partly supported by JSPS KAKENHI Grant Number 21H01661, 22K19078 and Toyota Mobility Foundation Hydrogen Initiative. References Z. Y. Wu, F. Y. Chen, B. Li, S. W. Yu, Y. Z. Finfrock, D. M. Meira, Q. Q. Yan, P. Zhu, M. X. Chen, T. W. Song, Z. Yin, H. W. Liang, S. Zhang, G. Wang and H. Wang, Nat. Mater., 22, 100 (2023). S. Chen, H. Huang, P. Jiang, K. Yang, J. Diao, S. Gong, S. Liu, M. Huang, H. Wang and Q. Chen, ACS Catal., 10, 1152 (2020). J. Su, R. Ge, K. Jiang, Y. Dong, F. Hao, Z. Tian, G. Chen and L. Chen, Adv Mater, 30, 1801351 (2018). Figure 1