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C‐doped SnO 2 nanostructure/ MoS 2 / p‐Si electrodes for visible light‐driven photoelectrochemical hydrogen evolution reaction
Author(s) -
Mallikarjuna Koduru,
Tekalgne Mahider Asmare,
Hasani Amirhossein,
Hong Sung Hyun,
Ahn Sang Hyun,
Kim Soo Young,
Kim Haekyoung
Publication year - 2021
Publication title -
international journal of energy research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.808
H-Index - 95
eISSN - 1099-114X
pISSN - 0363-907X
DOI - 10.1002/er.7111
Subject(s) - water splitting , materials science , hydrogen production , hydrogen , nanostructure , chemical engineering , context (archaeology) , electrochemistry , doping , substrate (aquarium) , nanotechnology , carbon fibers , electrode , optoelectronics , photocatalysis , chemistry , catalysis , organic chemistry , paleontology , biochemistry , oceanography , composite material , geology , composite number , engineering , biology
Summary Recently, the increase in the CO 2 content in the Earth's atmosphere causes global warming and the rapid consumption of fossil fuel resources such as coal and oil. Therefore, effort is required to create clean and sustainable energy resources to address these environmental issues. In this context, hydrogen evolution from water splitting‐based photoelectrochemical technologies plays a significant role as a zero CO 2 emission fuel. Here, we design and prepare carbon‐doped SnO 2 nanostructures by a simple single‐step thermal decomposition method and coated on a MoS 2 /p‐Si substrate for hydrogen evolution by photoelectrochemical water splitting. The C‐doped SnO 2 /MoS 2 /p‐Si shows enhanced activity in the hydrogen evolution reaction, with an onset potential of −0.17 V at 2.73 mA/cm 2 , and high stability for over 45 hours. In addition, the doping of carbon influences the shape of the nanostructures, inducing their transformation from cubical rods to polyhedral structures. This study provides a promising method for the fabrication of heterogeneous photoelectrocatalysts for overall water splitting.