B-Site Engineering in Ruddlesden–Popper Perovskites (A <sub>2</sub> BO <sub>4</sub> ) for H <sub>2</sub> O <sub>2</sub> Production with 4.85% of Solar-to-Chemical Efficiency
The electrochemical synthesis of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) via the oxygen reduction reaction (ORR) offers a promising alternative to the anthraquinone process, addressing environmental concerns without requiring expensive hydrogen. However, developing catalysts that selectively promote the two-electron ORR pathway while maintaining stability remains challenging. Here, we report Ruddlesden-Popper (RP) perovskite oxides as efficient catalysts for selective H<sub>2</sub>O<sub>2</sub> production. Among the tested LaSrBO<sub>4</sub> compositions (B = Ni, Co, Fe, Mn), LaSrNiO<sub>4</sub> (LSN) showed the best two-electron ORR selectivity (∼87%) and activity. Integrated into a photovoltaic-electrochemical system, LSN achieved a solar-to-chemical conversion efficiency of 4.85%, producing a H<sub>2</sub>O<sub>2</sub> production rate of 149.2 μmol cm<sup>-2</sup> h<sup>-1</sup> with good stability over 50 h. Density functional theory calculations attributed this performance to favorable H<sub>2</sub>O<sub>2</sub> formation and desorption kinetics at the Ni B-site. Overall, RP perovskites offer earth-abundant, efficient, and sustainable catalysts for electrochemical H<sub>2</sub>O<sub>2</sub> generation, providing an alternative to carbon- or noble-metal-based systems.
Authors
- Je Min Yu
- June Ho Choi (ORCID: https://orcid.org/0000-0002-5315-4180)
- Wook Jo (ORCID: https://orcid.org/0000-0002-7158-5654)
- Eunjae Jeong
- Ji-Wook Jang
- Jaewon Cho
- Hyunjoo Lee
- Sang-Goo Lee
- Youngchul Kim
- Geunsik Lee
Institutions
- Ibule Photonics (South Korea) (KR)
- Institute for Basic Science (KR)
- Ulsan National Institute of Science and Technology (KR)
Publication Details
- Journal
- Nano Letters
- Published
- 2026-02-19
- DOI
- https://doi.org/10.1021/acs.nanolett.5c05869
- Primary Topic
- Chemical Looping and Thermochemical Processes
- Type
- article
- Field-Weighted Citation Impact
- 0.00