Interfacial Engineering at Quantum Dot-Sensitized TiO2 Photoelectrodes for Ultrahigh Photocurrent Generation
- Authors
- Kim, Tea-Yon; Kim, Byung Su; Oh, Jong Gyu; Park, Seul Chan; Jang, Jaeyoung; Hamann, Thomas W.; Kang, Young Soo; Bang, Jin Ho; Giménez, Sixto; Kang, Yong Soo
- Issue Date
- Feb-2021
- Publisher
- American Chemical Society
- Keywords
- TiO2/QD; photoanode; photoelectrochemical cells; surface passivation layer; surface state; charge collection; photocurrent density
- Citation
- ACS Applied Materials and Interfaces, v.13, no.5, pp.6208 - 6218
- Indexed
- SCIE
SCOPUS
- Journal Title
- ACS Applied Materials and Interfaces
- Volume
- 13
- Number
- 5
- Start Page
- 6208
- End Page
- 6218
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/8022
- DOI
- 10.1021/acsami.0c19352
- ISSN
- 1944-8244
- Abstract
- Metal oxide semiconductor/chalcogenide quantum dot (QD) heterostructured photoanodes show photocurrent densities >30 mA/cm2 with ZnO, approaching the theoretical limits in photovoltaic (PV) cells. However, comparative performance has not been achieved with TiO2. Here, we applied a TiO2(B) surface passivation layer (SPL) on TiO2/QD (PbS and CdS) and achieved a photocurrent density of 34.59 mA/cm2 under AM 1.5G illumination for PV cells, the highest recorded to date. The SPL improves electron conductivity by increasing the density of surface states, facilitating multiple trapping/detrapping transport, and increasing the coordination number of TiO2 nanoparticles. This, along with impeded electron recombination, led to enhanced collection efficiency, which is a major factor for performance. Furthermore, SPL-treated TiO2/QD photoanodes were successfully exploited in photoelectrochemical water splitting cells, showing an excellent photocurrent density of 14.43 mA/cm2 at 0.82 V versus the Reversible Hydrogen Electrode (RHE). These results suggest a new promising strategy for the development of high-performance photoelectrochemical devices.
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