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Monolayer NiIr-Layered Double Hydroxide as a Long-Lived Efficient Oxygen Evolution Catalyst for Seawater Splitting

Hanhui YouFujian Institute of Research on the Structure of MatterDongshuang WuDivision of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, JapanDuan‐Hui SiState Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, P. R. ChinaMinna CaoUniversity of Chinese Academy of Sciences, Beijing 100049, P.R. ChinaFanfei SunShanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201204, P. R. ChinaHao ZhangShanghai Institute of Applied PhysicsHuimin WangState Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, P. R. ChinaTian‐Fu LiuState Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, P. R. ChinaRong CaoUniversity of Chinese Academy of Sciences, Beijing 100049, P.R. China
2022en
ABI

Annotatsiya

Promoting the oxygen evolution reaction (OER) with saline water is highly desired to realize seawater splitting. This requires OER catalysts to resist serious corrosion and undesirable chloride oxidation. We introduce a 5d transition metal, Ir, to develop a monolayer NiIr-layered double hydroxide (NiIr-LDH) as the catalyst with enhanced OER performance for seawater splitting. The NiIr-LDH catalyst delivers 500 mA/cm2 at only 361 mV overpotential with ∼99% O2 Faradaic efficiency in alkaline seawater, which is more active than commercial IrO2 (763 mV, 23%) and the best known OER catalyst NiFe-LDH (530 mV, 92%). Moreover, it shows negligible activity loss at up to 650 h chronopotentiometry measurements at an industrial level (500 mA/cm2), while commercial IrO2 and NiFe-LDH rapidly deactivated within 0.2 and 10 h, respectively. The incorporation of Ir into the Ni(OH)2 layer greatly altered the electron density of Ir and Ni sites, which was revealed by X-ray absorption fine structure and density functional theory (DFT) calculations. Coupling the electrochemical measurements and in situ Raman spectrum with DFT calculations, we further confirm that the generation of rate-limiting intermediate *O and *OOH species was accelerated on Ni and Ir sites, respectively, which is responsible for the high seawater splitting performance. Our results also provide an opportunity to fabricate LDH materials containing 5d metals for applications beyond seawater splitting.

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