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Title: Light-Induced Charge Transport within a Single Asymmetric Nanowire

Journal Article · · Nano Letters
DOI:https://doi.org/10.1021/nl201798e· OSTI ID:1168603
 [1];  [1];  [2];  [1]
  1. Univ. of California, Berkeley, CA (United States); Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)
  2. Univ. of California, Berkeley, CA (United States)

Artificial photosynthetic systems using semiconductor materials have been explored for more than three decades in order to store solar energy in chemical fuels such as hydrogen. By mimicking biological photosynthesis with two light-absorbing centers that relay excited electrons in a nanoscopic space, a dual-band gap photoelectrochemical (PEC) system is expected to have higher theoretical energy conversion efficiency than a single band gap system. This work demonstrates the vectorial charge transport of photo-generated electrons and holes within a single asymmetric Si/TiO2 nanowire using Kelvin probe force microscopy (KPFM). Under UV illumination, higher surface potential was observed on the n-TiO₂ side, relative to the potential of the p-Si side, as a result of majority carriers’ recombination at the Si/TiO₂ interface. These results demonstrate a new approach to investigate charge separation and transport in a PEC system. This asymmetric nanowire heterostructure, with a dual band gap configuration and simultaneously exposed anode and cathode surfaces represents an ideal platform for the development of technologies for the generation of solar fuels, although better photoanode materials remain to be discovered.

Research Organization:
Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
Sponsoring Organization:
USDOE Office of Science (SC)
DOE Contract Number:
DE-AC02-05CH11231
OSTI ID:
1168603
Report Number(s):
LBNL-5602E
Journal Information:
Nano Letters, Vol. 11, Issue 9; Related Information: Journal Publication Date: 07/18/2011; ISSN 1530-6984
Publisher:
American Chemical Society
Country of Publication:
United States
Language:
English