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Bioinspired Design of Hybrid Polymer Catalysts with Multicopper Sites for Oxygen Reduction
Author(s) -
Jin Lei,
Thanneeru Srinivas,
Cintron Daniel,
He Jie
Publication year - 2020
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.202001333
Subject(s) - catalysis , pyrene , chemistry , stacking , polymer , transition metal , bimetallic strip , electrocatalyst , oxygen , supramolecular chemistry , polymer chemistry , oxygen reduction , rational design , combinatorial chemistry , inorganic chemistry , materials science , nanotechnology , organic chemistry , electrode , electrochemistry , molecule
Abstract Cu‐containing metalloenzymes are known to catalyze oxygen activation through cooperative catalysis. In the current work, we report the design of synthetic polymer Cu catalysts using pyrene‐labelled poly(2‐hydroxy‐3‐dipicolylamino) propyl methacrylate (Py‐PGMADPA) to coordinate multiple Cu sites along polymer chains. The catalysts feature a pyrene end group that can form supramolecular π‐π stacking with conductive carbon to allow efficient immobilization of catalysts to the graphite electrode. Cu‐containing Py‐PGMADPA was examined for electrocatalytic oxygen reduction. The hybrid catalyst showed an onset potential of 0.5 V (vs. RHE) at pH 7 and 0.79 V at pH 13. The kinetic study indicated that the catalyst had a 2e − reduction of oxygen mainly mediated by Cu + centers. We demonstrated the importance of cooperative catalysis among Cu sites which did not exist for other transition metal ions, like Mn 2+ , Fe 2+ , Co 2+ , and Ni 2+ . The confinement of polymer chains promotes the activity and stabilizes Cu catalysts even at an extremely low Cu loading. The rational design of bioinspired polymer catalysts offers an alternative way to prepare synthetic mimics of metalloenzymes.