Xia, Fengjie, Pan, Mu, Mu, Shichun, Malpass-Evans, Richard, Carta, Mariolino ![]() ![]() |
Abstract
Two polymers (i) the polymer of intrinsic microporosity (or PIM) ethanoanthracene TB-PIM (P1, PIM-EA-TB, MW 70 kDa, BET surface area 1027 m2 g−1) and (ii) the structurally less rigid polymer based on dimethyldiphenylmethane units (P2, BDMPM-TB, MW 100 kDa, BET surface area 47 m2g−1) are compared to highlight the benefits of the newly emerging PIM membrane materials in electrocatalysis and nanostructure formation. Binding sites and binding ability/capacity in aqueous environments are compared in films deposited onto glassy carbon electrodes for (i) indigo carmine dianion immobilisation (weakly binding from water–ethanol) and (ii) PdCl42− immobilisation (strongly binding from acidic media). Nano-lamella growth for Pd metal during electro-reduction of PdCl42− is observed. Electrocatalytic oxidation of formic acid (at pH 6) is investigated for P1 and P2 as a function of film thickness. The more rigid high BET surface area PIM material P1 exhibits “open-pore” characteristics with much more promising electrocatalytic activity at Pd lamella within polymer pores.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Chemistry Cardiff Catalysis Institute (CCI) |
Subjects: | Q Science > QD Chemistry |
Uncontrolled Keywords: | Microporosity; Nanostructure; Fuel cell; Formic acid; Electrocatalysis |
Publisher: | Elsevier |
ISSN: | 0013-4686 |
Funders: | EPSRC |
Last Modified: | 06 Jan 2024 04:56 |
URI: | https://orca.cardiff.ac.uk/id/eprint/59985 |
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