n-ZrS/p-ZrOS photoanodes with NiOOH/FeOOH oxygen evolution catalysts for photoelectrochemical water oxidation
Creators
- 1. Department of Chemistry, National University of Singapore, Singapore, 117543 (Singapore)
- 2. State Key Laboratory of Radio Frequency Heterogeneous Integration, and International Collaborative Laboratory of 2D Materials for Optoelectronics Science and Technology of Ministry of Education, Institute of Microscale Optoelectronics, Shenzhen University, Shenzhen, 518060 (China)
- 3. Joint School of National University of Singapore and Tianjin University, International Campus of Tianjin University, Binhai New City, Fuzhou, 350207 (China)
- 4. Department of Chemistry, South Kensington Campus, Imperial College London, London, SW7 2AZ (United Kingdom)
- 5. Department of Physics, National University of Singapore, Singapore, 117542 (Singapore)
Description
Photoelectrochemical water splitting offers a promising approach for carbon neutrality, but its commercial prospects are still hampered by a lack of efficient and stable photoelectrodes with earth-abundant materials. Here, we report a strategy to construct an efficient photoanode with a coaxial nanobelt structure, comprising a buried-ZrS/ZrOS n - p junction, for photoelectrochemical water splitting. The p-type ZrOS layer, formed on the surface of the n-type ZrS nanobelt through a pulsed-ozone-treatment method, acts as a hole collection layer for hole extraction and a protective layer to shield the photoanode from photocorrosion. The resulting ZrS/ZrOS photoanode exhibits light harvesting with good photo-to-current efficiencies across the whole visible region to over 650 nm. By further employing NiOOH/FeOOH as the oxygen evolution reaction cocatalyst, the ZrS/ZrOS/NiOOH/FeOOH photoanode yields a photocurrent density of ~9.3 mA cm at 1.23 V versus the reversible hydrogen electrode with an applied bias photon-to-current efficiency of ~3.2 % under simulated sunlight irradiation in an alkaline solution (pH=13.6). The conformal ZrOS layer enables ZrS/ZrOS/NiOOH/FeOOH photoanode operation over 1000 hours in an alkaline solution without obvious performance degradation. This study, offering a promising approach to fabricate efficient and durable photoelectrodes with earth-abundant materials, advances the frontiers of photoelectrochemical water splitting. (© 2024 Wiley-VCH GmbH)
Availability note (English)
Available from: http://dx.doi.org/10.1002/anie.202414209Additional details
Publishing Information
- Journal Title
- Angewandte Chemie (International Edition)
- Journal Volume
- 64
- Journal Issue
- 2
- Journal Page Range
- p. 1-10
- ISSN
- 1433-7851
- CODEN
- ACIEF5
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- CATALYSTS; CURRENT DENSITY; IRON HYDROXIDES; LAYERS; NICKEL OXIDES; OXIDATION; PHOTOANODES; PHOTOELECTROCHEMICAL CELLS; P-N JUNCTIONS; WATER; ZIRCONIUM OXIDES; ZIRCONIUM SULFIDES
- Descriptors DEC
- ANODES; CHALCOGENIDES; CHEMICAL REACTIONS; ELECTROCHEMICAL CELLS; ELECTRODES; HYDROGEN COMPOUNDS; HYDROXIDES; IRON COMPOUNDS; NICKEL COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; SEMICONDUCTOR JUNCTIONS; SULFIDES; SULFUR COMPOUNDS; TRANSITION ELEMENT COMPOUNDS; ZIRCONIUM COMPOUNDS
Optional Information
- Notes
- AID: e202414209