TY - JOUR
T1 - Water oxidation electrocatalysis using ruthenium coordination oligomers adsorbed on multiwalled carbon nanotubes
AU - Hoque, Md Asmaul
AU - Gil-Sepulcre, Marcos
AU - de Aguirre, Adiran
AU - Elemans, Johannes A.A.W.
AU - Moonshiram, Dooshaye
AU - Matheu, Roc
AU - Shi, Yuanyuan
AU - Benet-Buchholz, Jordi
AU - Sala, Xavier
AU - Malfois, Marc
AU - Solano, Eduardo
AU - Lim, Joohyun
AU - Garzón-Manjón, Alba
AU - Scheu, Christina
AU - Lanza, Mario
AU - Maseras, Feliu
AU - Gimbert-Suriñach, Carolina
AU - Llobet, Antoni
N1 - Generated from Scopus record by KAUST IRTS on 2021-03-16
PY - 2020/11/1
Y1 - 2020/11/1
N2 - Photoelectrochemical cells that utilize water as a source of electrons are one of the most attractive solutions for the replacement of fossil fuels by clean and sustainable solar fuels. To achieve this, heterogeneous water oxidation catalysis needs to be mastered and properly understood. The search continues for a catalyst that is stable at the surface of electro(photo)anodes and can efficiently perform this reaction at the desired neutral pH. Here, we show how oligomeric Ru complexes can be anchored on the surfaces of graphitic materials through CH–π interactions between the auxiliary ligands bonded to Ru and the hexagonal rings of the graphitic surfaces, providing control of their molecular coverage. These hybrid molecular materials behave as molecular electroanodes that catalyse water oxidation to dioxygen at pH 7 with high current densities. This strategy for the anchoring of molecular catalysts on graphitic surfaces can potentially be extended to other transition metals and other catalytic reactions. [Figure not available: see fulltext.]
AB - Photoelectrochemical cells that utilize water as a source of electrons are one of the most attractive solutions for the replacement of fossil fuels by clean and sustainable solar fuels. To achieve this, heterogeneous water oxidation catalysis needs to be mastered and properly understood. The search continues for a catalyst that is stable at the surface of electro(photo)anodes and can efficiently perform this reaction at the desired neutral pH. Here, we show how oligomeric Ru complexes can be anchored on the surfaces of graphitic materials through CH–π interactions between the auxiliary ligands bonded to Ru and the hexagonal rings of the graphitic surfaces, providing control of their molecular coverage. These hybrid molecular materials behave as molecular electroanodes that catalyse water oxidation to dioxygen at pH 7 with high current densities. This strategy for the anchoring of molecular catalysts on graphitic surfaces can potentially be extended to other transition metals and other catalytic reactions. [Figure not available: see fulltext.]
UR - http://www.nature.com/articles/s41557-020-0548-7
UR - http://www.scopus.com/inward/record.url?scp=85091606743&partnerID=8YFLogxK
U2 - 10.1038/s41557-020-0548-7
DO - 10.1038/s41557-020-0548-7
M3 - Article
C2 - 32989272
SN - 1755-4349
VL - 12
SP - 1060
EP - 1066
JO - Nature Chemistry
JF - Nature Chemistry
IS - 11
ER -