Mixed B-site ruddlesden-popper phase Sr2(Ru Ir1-)O4 enables enhanced activity for oxygen evolution reaction

نویسندگان

چکیده

Development of high performance electrocatalysts for oxygen evolution reaction (OER) in acidic media remains a challenge direct water splitting using an electrolyzer. Recently, Ruddlesden-Popper phase Sr2IrO4 was discovered to be efficient OER catalyst because its unique structure, which consists layers both rock salt and perovskite phases simultaneously. In this study, we prepared series B-site mixed, Sr2(RuxIr1?x)O4 examined their electrocatalytic properties media. Through partial substitution Ru the materials, achieved much enhanced electrocatalysts, among Sr2(Ru0.5Ir0.5)O4 exhibited best catalytic activity with current density 8.06 mA/cm2 at 1.55 V Tafel slope 47 mV/dec. This is three times higher than that Sr2IrO4. The mixed retained good stability conditions > 24 h 10 mA/cm2. A range techniques were used characterize crystal electronic structures samples. Our data indicate improved can correlated formation level hydroxyl groups overlap between Ir/Ru 4d O 2p orbitals, revealing new way design by regulating composition structures.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Controlling Oxygen Mobility in Ruddlesden–Popper Oxides

Discovering new energy materials is a key step toward satisfying the needs for next-generation energy conversion and storage devices. Among the various types of oxides, Ruddlesden-Popper (RP) oxides (A₂BO₄) are promising candidates for electrochemical energy devices, such as solid oxide fuel cells, owing to their attractive physicochemical properties, including the anisotropic nature of oxygen ...

متن کامل

Oxygen Evolution at Manganite Perovskite Ruddlesden-Popper Type Particles: Trends of Activity on Structure, Valence and Covalence

An improved understanding of the correlation between the electronic properties of Mn-O bonds, activity and stability of electro-catalysts for the oxygen evolution reaction (OER) is of great importance for an improved catalyst design. Here, an in-depth study of the relation between lattice structure, electronic properties and catalyst performance of the perovskite Ca1-xPrxMnO₃ and the first-orde...

متن کامل

Synthesis and Structure of LaSr2CuTiO6.5: A New Oxygen-Deficient Ruddlesden-Popper Phase

The structure of LaSr2CuTiO6.5, a novel (ABO3)nAO n ) 2 Ruddlesden-Popper phase, has been solved by powder X-ray diffraction and electron microscopy. The diffraction patterns are consistent with I4/mmm symmetry, with tetragonal lattice parameters a ) 3.8816(1) Å and c ) 20.296(2) Å. The structure of LaSr2CuTiO6.5 is similar to Sr3Ti2O7, with copper and titanium disordered over the single B-cati...

متن کامل

Synthesis and photocatalytic activity of K2CaNaNb3O10, a new Ruddlesden-Popper phase layered perovskite.

A new three-layer perovskite oxide with the Ruddlesden-Popper (R-P) phase, K2CaNaNb3O10, and its protonated form were synthesised and their photocatalytic performance was compared to that of KCa2Nb3O10 or the protonated form with the Dion-Jacobson (D-J) structure in terms of H2 and O2 evolution. K2CaNaNb3O10 exhibited a higher activity for O2 evolution than KCa2Nb3O10 when IO3- was used as an e...

متن کامل

Symmetry analysis for the Ruddlesden-Popper systems Ca3Mn2O7 and Ca3Ti2O7

We perform a symmetry analysis of the zero-temperature instabilities of the tetragonal phase of Ca3Mn2O7 and Ca3Ti2O7 which is stable at high temperature.We introduce order parameters to characterize each of the possible lattice distortions to construct a Landau free energy which elucidates the proposed group-subgroup relations for structural transitions in these systems. We include the couplin...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Journal of Energy Chemistry

سال: 2022

ISSN: ['2096-885X', '2095-4956']

DOI: https://doi.org/10.1016/j.jechem.2022.02.051