Constructing Sequential Type II Heterojunction CQDs/Bi2S3/TiNbO Photoanode with Superior Charge Transfer Capability Toward Stable Photoelectrochemical Water Splitting

• Published in: ACS applied materials & interfaces 2024-04, Vol.16 (13), p.16062-16074
• Main Authors: Pan, Yanjie, Dong, Zhenbiao, Qin, Dongmei, Liu, Baopeng, Cui, Lulu, Han, Sheng, Lin, Hualin
• Format: Article
• Language: English
• Subjects: absorption; carbon; electric current; electrical conductivity; electrodes; Energy, Environmental, and Catalysis Applications; hydrogen; liquid-solid interface; nanotubes
• ISSN: 1944-8244; 1944-8252; 1944-8252
• DOI: 10.1021/acsami.3c17726

Efficient charge transfer and light-trapping units are pivotal prerequisites in the realm of Ti-based photoanode photoelectrochemical (PEC) water splitting. In this work, we successfully synthesized a ternary carbon quantum dots/Bi2S3 quantum dots/Nb-doped TiO2 nanotube arrays (CQDs/Bi2S3/TiNbO) composite photoanode for PEC water splitting. CQDs/Bi2S3/TiNbO composite photoanode exhibited a considerably elevated photocurrent density of 8.80 mA cm–2 at 1.23 V vs the reversible hydrogen electrode, which was 20.00 times better than that of TiO2 (0.44 mA cm–2). Furthermore, the CQDs/Bi2S3/TiNbO composite photoanode attested to exceptional stability, maintaining 92.54% of its initial current after 5 h of stability measurement. Nb-doping boosted the electrical conductivity, facilitating charge transfer at the solid–liquid interface. Moderate amounts of Bi2S3 quantum dots (QDs) and CQDs deposited on TiNbO provided abundant active sites for the electrolyte–photoanode interaction. Simultaneously, Bi2S3 QDs and CQDs synergistically functioned as light-trapping units to broaden the light absorption range from 396 to 530 nm, stimulating increased carrier generation within the composite photoanode. In comparison with pristine TiO, CQDs/Bi2S3/TiNbO photoanodes possessed a superior ability to promote interfacial reactions. This study may provide a strategy for developing high-performance Ti-based photoanodes with efficient charge transfer and light trapping units for highly driving solar-to-hydrogen conversion.