Nanostructure-assisted charge transfer in α-Fe2O3/g-C3N4 heterojunctions for efficient and highly stable photoelectrochemical water splitting

2020 ◽  
Vol 49 (32) ◽  
pp. 11317-11328 ◽  
Author(s):  
Nurul Affiqah Arzaee ◽  
Mohamad Firdaus Mohamad Noh ◽  
Nur Suraya Haziqah Mohd Ita ◽  
Nurul Aida Mohamed ◽  
Siti Nur Farhana Mohd Nasir ◽  
...  

Modification of the nanostructural features of an α-Fe2O3/g-C3N4 heterojunction photoanode contributes to a threefold stability enhancement in photoelectrochemical water splitting owing to the efficient charge transfer dynamics.

2020 ◽  
Vol 8 (40) ◽  
pp. 20963-20969 ◽  
Author(s):  
Wei Chen ◽  
Guo-Bo Huang ◽  
Hao Song ◽  
Jian Zhang

An efficient charge transfer channel for improving the photocatalytic water splitting activity and durability of CdS without sacrificial agents.


2016 ◽  
Vol 7 (9) ◽  
pp. 6076-6082 ◽  
Author(s):  
Ailong Li ◽  
Zhiliang Wang ◽  
Heng Yin ◽  
Shengyang Wang ◽  
Pengli Yan ◽  
...  

The key to phase junctions for efficient charge separation is to consider both the phase alignment and interface structure.


2019 ◽  
Vol 375 ◽  
pp. 389-398 ◽  
Author(s):  
Yixuan Gao ◽  
Shihao Zhang ◽  
Yishi Wu ◽  
Yang Tian ◽  
Hongbing Fu ◽  
...  

2021 ◽  
Author(s):  
Can Li ◽  
Ruotian Chen ◽  
Zefeng Ren ◽  
Yu Liang ◽  
Thomas Dittrich ◽  
...  

Abstract Water-splitting reactions using photocatalyst particles are promising routes for solar fuel production1-4. Photoinduced charge transfer from a photocatalyst to catalytic surface sites is key in ensuring photocatalytic efficiency5; however, it is challenging to understand this process, which spans a wide spatiotemporal range from nanometers to micrometers and from femtoseconds to seconds6-8. Although the steady-state charge distribution on single photocatalyst particles has been mapped using microscopic techniques9-11 and the averaged charge transfer dynamics in photocatalyst aggregations have been revealed via time-resolved spectroscopy12,13, spatiotemporally evolving charge transfer processes in single photocatalyst particles cannot be tracked, and the mechanism of charge transfer is unknown. Here, we report spatiotemporally resolved surface photovoltage measurements on Cu2O photocatalyst particles to map complete charge transfer processes throughout the femtosecond to second time scale at the single-particle level. We found that photogenerated electrons are transferred to the catalytic surface ballistically on a sub-picosecond timescale and are retained at this location for the duration, whereas photogenerated holes are transferred to a spatially separated surface and stabilized via selective trapping on a microsecond timescale. We demonstrate that these ballistic electron transfer and anisotropic trapping regimes, which challenge the classical perception of the drift–diffusion model, contribute to efficient charge separation in photocatalysis and improve the photocatalytic performance. We anticipate our findings to demonstrate the universality of other photoelectronic devices and facilitate the rational design of photocatalysts.


Author(s):  
Umesh Prasad ◽  
James Luke Young ◽  
Justin C. Johnson ◽  
Deborah McGott ◽  
Hengfei Gu ◽  
...  

Photoanodes containing a WO3/BiVO4 heterojunction have demonstrated promising photoelectrochemical water splitting performance, but the ability to effectively passivate the WO3/BiVO4 interface has limited charge transport and collection. Here, the WO3/BiVO4...


Sign in / Sign up

Export Citation Format

Share Document