Platinum-decorated carbon nanotubes for hydrogen oxidation and proton reduction in solid acid electrochemical cells† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c4sc03003f
نویسندگان
چکیده
Pt-decorated carbon nanotubes (Pt-CNTs) were used to enhance proton reduction and hydrogen evolution in solid acid electrochemical cells based on the proton-conducting electrolyte CsH2PO4. The carbon nanotubes served as interconnects to the current collector and as a platform for interaction between the Pt and CsH2PO4, ensuring minimal catalyst isolation and a large number density of active sites. Particle size matching was achieved by using electrospray deposition to form sub-micron to nanometric CsH2PO4. A porous composite electrode was fabricated from electrospray deposition of a solution of Pt-CNTs and CsH2PO4. Using AC impedance spectroscopy and cyclic voltammetry, the total electrode overpotential corresponding to proton reduction and hydrogen oxidation of the most active electrodes containing just 0.014 mg cm 1 of Pt was found to be 0.1 V (or 0.05 V per electrode) at a current density of 42 mA cm 2 for a measurement temperature of 240 C and a hydrogen-steam atmosphere. The zero bias electrode impedance was 1.2 U cm, corresponding to a Pt utilization of 61 S mg , a 3-fold improvement over state-of-the-art electrodes with a 50 decrease in Pt loading.
منابع مشابه
Platinum-decorated carbon nanotubes for hydrogen oxidation and proton reduction in solid acid electrochemical cells.
Pt-decorated carbon nanotubes (Pt-CNTs) were used to enhance proton reduction and hydrogen evolution in solid acid electrochemical cells based on the proton-conducting electrolyte CsH2PO4. The carbon nanotubes served as interconnects to the current collector and as a platform for interaction between the Pt and CsH2PO4, ensuring minimal catalyst isolation and a large number density of active sit...
متن کاملTandem redox mediator/Ni(ii) trihalide complex photocycle for hydrogen evolution from HCl† †Electronic supplementary information (ESI) available: Experimental procedures and time-dependent photochemical data; transient absorption spectroscopy and electrochemical experimental details. CCDC 992218–992221. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c4sc02357a Click here for additional data file. Click here for additional data file.
متن کامل
Metal-free electrocatalytic hydrogen oxidation using frustrated Lewis pairs and carbon-based Lewis acids† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c5sc04564a Click here for additional data file.
Whilst hydrogen is a potentially clean fuel for energy storage and utilisation technologies, its conversion to electricity comes at a high energetic cost. This demands the use of rare and expensive precious metal electrocatalysts. Electrochemical-frustrated Lewis pairs offer a metal-free, CO tolerant pathway to the electrocatalysis of hydrogen oxidation. They function by combining the hydrogen-...
متن کاملLaser-induced pinpoint hydrogen evolution from benzene and water using metal free single-walled carbon nanotubes with high quantum yields† †Electronic supplementary information (ESI) available: GC and HPLC analyses for products characterisation (Fig. S1–S3 and S5), time course data of H2 evolution in various solvents (S4), IR (S6), TG (S7) and experimental details (S8). See DOI: 10.1039/c4sc02269f Click here for additional data file.
متن کامل