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CO 2 Overall Splitting by a Bifunctional Metal‐Free Electrocatalyst
Author(s) -
Ghausi Muhammad Arsalan,
Xie Jiafang,
Li Qiaohong,
Wang Xueyuan,
Yang Rui,
Wu Maoxiang,
Wang Yaobing,
Dai Liming
Publication year - 2018
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201807571
Subject(s) - overpotential , electrocatalyst , oxygen evolution , bifunctional , water splitting , materials science , tafel equation , inorganic chemistry , chemistry , electrochemistry , catalysis , electrode , organic chemistry , photocatalysis
Abstract Photo/electrochemical CO 2 splitting is impeded by the low cost‐effective catalysts for key reactions: CO 2 reduction (CDRR) and water oxidation. A porous silicon and nitrogen co‐doped carbon (SiNC) nanomaterial by a facile pyrolyzation was developed as a metal‐free bifunctional electrocatalyst. CO 2 ‐to‐CO and oxygen evolution (OER) partial current density under neutral conditions were enhanced by two orders of magnitude in the Tafel regime on SiNC relative to single‐doped comparisons beyond their specific area gap. The photovoltaic‐driven CO 2 splitting device with SiNC electrodes imitating photosynthesis yielded an overall solar‐to‐chemical efficiency of advanced 12.5 % (by multiplying energy efficiency of CO 2 splitting cell and photovoltaic device) at only 650 mV overpotential. Mechanism studies suggested the elastic electron structure of −Si(O)−C−N− unit in SiNC as the highly active site for CDRR and OER simultaneously by lowering the free energy of CDRR and OER intermediates adsorption.