Ultrastable halide perovskite CsPbBr<sub>3</sub> photoanodes achieved with electrocatalytic glassy-carbon and boron-doped diamond sheets.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 38555394.
- Also identified by DOI 10.1038/s41467-024-47100-2 and PMC identifier 10981704.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Halide perovskites exhibit exceptional optoelectronic properties for photoelectrochemical production of solar fuels and chemicals but their instability in aqueous electrolytes hampers their application. Here we present ultrastable perovskite CsPbBr<sub>3</sub>-based photoanodes achieved with both multifunctional glassy carbon and boron-doped diamond sheets coated with Ni nanopyramids and NiFeOOH. These perovskite photoanodes achieve record operational stability in aqueous electrolytes, preserving 95% of their initial photocurrent density for 168 h of continuous operation with the glassy carbon sheets and 97% for 210 h with the boron-doped diamond sheets, due to the excellent mechanical and chemical stability of glassy carbon, boron-doped diamond, and nickel metal. Moreover, these photoanodes reach a low water-oxidation onset potential close to +0.4 V<sub>RHE</sub> and photocurrent densities close to 8 mA cm<sup>-2</sup> at 1.23 V<sub>RHE</sub>, owing to the high conductivity of glassy carbon and boron-doped diamond and the catalytic activity of NiFeOOH. The applied catalytic, protective sheets employ only earth-abundant elements and straightforward fabrication methods, engineering a solution for the success of halide perovskites in stable photoelectrochemical cells.