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Hydrogen‐Bonding Triggered Assembly to Configure Hollow Carbon Nanosheets for Highly Efficient Tri‐Iodide Reduction
Author(s) -
Chang Jiangwei,
Song Xuedan,
Yu Chang,
Yu Jinhe,
Ding Yiwang,
Yao Chun,
Zhao Zongbin,
Qiu Jieshan
Publication year - 2020
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.202006270
Subject(s) - materials science , adsorption , nanotechnology , carbon fibers , catalysis , aqueous solution , iodide , chemical engineering , molecule , noble metal , metal , inorganic chemistry , organic chemistry , composite material , chemistry , composite number , engineering , metallurgy
Carbon materials have rapidly grown as highly promising candidates to replace noble metal catalysts in energy storage/conversion technologies. In this work, a strategy of hydrogen‐bonding triggered assembly to configure hollow carbon nanosheets by applying Silicalite‐1 as a substrate in the aqueous solution of dopamine is reported. Remarkably, the combined density functional theory modelling and experimental verification present a molecule/nano‐scale insight into the nature of the bonding behavior during the fabrication process. It is demonstrated that the SiOH on the surface of Silicalite‐1 acts as an anchor and that it is energetically favorable to pre‐adsorb the building blocks of polydopamine by hydrogen‐bonding, which triggers the subsequent assembly. As an example, the as‐prepared hollow carbon nanosheets with unique structure can efficiently catalyze tri‐iodide reduction and a power conversion efficiency up to 8.58%.