TY - JOUR
T1 - Plasmonic Au Grid-CdSe Heteropatterned Film by Topochemistry and CdCl2 Surface Passivation for Photoelectrochemical Hydrogen Evolution
AU - Wang, Jiale
AU - Li, Xinyuan
AU - Chen, Akang
AU - Wu, Bohan
AU - Li, Shouyuan
AU - Zhu, Chuwei
AU - Zhang, Xurui
AU - Hou, Tailei
AU - Wei, Tianxin
AU - Zhang, Jiatao
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025/4/21
Y1 - 2025/4/21
N2 - Constructing patterned film photoanodes with economizing raw chemicals but enhancing photoelectrochemical (PEC) performance is attractive for practical applications. However, simultaneously optimizing light scattering and interfacial charge transfer through plasmonic enhancement remains challenging. Herein, we developed a novel plasmonic photoanode featuring Au grids and a nanometer-thick CdSe layer (Au grid-CdSe) with well-organized heterointerfaces, fabricated via a facile colloidal topochemical strategy. This design leverages the synergistic coupling between plasmons and excitons in plasmonic heteropatterned films. The underlying patterned Au grids serve dual functions: as an electron collector and light reflector. Their highly ordered Bragg structure effectively scatters incident light into the ultrathin CdSe layer. Furthermore, CdCl2 surface passivation of the Au(grid)-CdSe heteropatterned photoanode, based on this unique light absorption/reflector architecture, yielded a photocurrent density of 4.51 mA cm-2, representing significant enhancement. Compared to similarly prepared Au-CdSe heterofilms, the passivated Au(grid)-CdSe heteropatterned films exhibited 2.0-fold higher PEC hydrogen evolution performance, maintained excellent stability for over 26 h, and reduced Au consumption by 32%. This strategy offers a novel pathway for improving the performance of semiconductor-based optoelectronic devices.
AB - Constructing patterned film photoanodes with economizing raw chemicals but enhancing photoelectrochemical (PEC) performance is attractive for practical applications. However, simultaneously optimizing light scattering and interfacial charge transfer through plasmonic enhancement remains challenging. Herein, we developed a novel plasmonic photoanode featuring Au grids and a nanometer-thick CdSe layer (Au grid-CdSe) with well-organized heterointerfaces, fabricated via a facile colloidal topochemical strategy. This design leverages the synergistic coupling between plasmons and excitons in plasmonic heteropatterned films. The underlying patterned Au grids serve dual functions: as an electron collector and light reflector. Their highly ordered Bragg structure effectively scatters incident light into the ultrathin CdSe layer. Furthermore, CdCl2 surface passivation of the Au(grid)-CdSe heteropatterned photoanode, based on this unique light absorption/reflector architecture, yielded a photocurrent density of 4.51 mA cm-2, representing significant enhancement. Compared to similarly prepared Au-CdSe heterofilms, the passivated Au(grid)-CdSe heteropatterned films exhibited 2.0-fold higher PEC hydrogen evolution performance, maintained excellent stability for over 26 h, and reduced Au consumption by 32%. This strategy offers a novel pathway for improving the performance of semiconductor-based optoelectronic devices.
UR - http://www.scopus.com/inward/record.url?scp=105002990781&partnerID=8YFLogxK
U2 - 10.1021/acs.inorgchem.5c00643
DO - 10.1021/acs.inorgchem.5c00643
M3 - Article
AN - SCOPUS:105002990781
SN - 0020-1669
VL - 64
SP - 7639
EP - 7648
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 15
ER -