TY - JOUR
T1 - Light-assisted electrochemical water-splitting at very low bias voltage using metal-free polythiophene as photocathode at high pH in a full-cell setup
AU - Oka, Kouki
AU - Tsujimura, Orie
AU - Suga, Takeo
AU - Nishide, Hiroyuki
AU - Winther-Jensen, Bjorn
N1 - Funding Information:
This work was partially supported by Grants-in-Aids for Scientific Research (16K05922 and 18H03921) and by the Top Global University Project from MEXT, Japan and the Research Institute for Science and Engineering, Waseda University. T. S. acknowledges the Grants-in-Aids for Scientific Research on Innovative Areas (New Polymeric Materials Based on Element Blocks, 15H00766 and 25102541). K. O. acknowledges the Leading Graduate Program in Science and Engineering, Waseda University, from MEXT, Japan.
Publisher Copyright:
© 2018 The Royal Society of Chemistry.
PY - 2018/5
Y1 - 2018/5
N2 - We report the use of polyterthiophenes (PTTh) as a rare, combined light-harvester and catalyst for the hydrogen evolution reaction at high pH. Illuminated PTTh in combination with a MnOx anode in a two-electrode setup exhibited stable water-splitting at a bias-potential of only 0.3 V at pH 12. This confirms that PTTh used as photocathode can produce photovoltages of at least 900 mV for the hydrogen evolution reaction at high pH and is therefore a suitable match for traditional water-oxidation catalysts such as MnOx, CoOx, and RuOx. Films of PTTh were fabricated using a novel, metal-free method where iodine vapor is used as oxidant; thus, previously observed interference from metal residuals was omitted and thereby a gravimetric photo electrocatalytic conversion rate of 330 mmol(H2) h-1 g-1 was achieved in phosphate buffer (pH 7) at 0 V vs. RHE. A striking property of this new strand of polythiophene was an "inverse" correlation (compared to that predicted using the Nernstian relationship) between the onset potential for the light-assisted water reduction reaction and pH: the potential (vs. RHE) required for a given current was more positive at higher pH, which is not observed for other (photo-) electrocatalytic materials, and indicates that the charge neutralization of PTTh (rather than the pH) guides the onset potential.
AB - We report the use of polyterthiophenes (PTTh) as a rare, combined light-harvester and catalyst for the hydrogen evolution reaction at high pH. Illuminated PTTh in combination with a MnOx anode in a two-electrode setup exhibited stable water-splitting at a bias-potential of only 0.3 V at pH 12. This confirms that PTTh used as photocathode can produce photovoltages of at least 900 mV for the hydrogen evolution reaction at high pH and is therefore a suitable match for traditional water-oxidation catalysts such as MnOx, CoOx, and RuOx. Films of PTTh were fabricated using a novel, metal-free method where iodine vapor is used as oxidant; thus, previously observed interference from metal residuals was omitted and thereby a gravimetric photo electrocatalytic conversion rate of 330 mmol(H2) h-1 g-1 was achieved in phosphate buffer (pH 7) at 0 V vs. RHE. A striking property of this new strand of polythiophene was an "inverse" correlation (compared to that predicted using the Nernstian relationship) between the onset potential for the light-assisted water reduction reaction and pH: the potential (vs. RHE) required for a given current was more positive at higher pH, which is not observed for other (photo-) electrocatalytic materials, and indicates that the charge neutralization of PTTh (rather than the pH) guides the onset potential.
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U2 - 10.1039/c7ee03669h
DO - 10.1039/c7ee03669h
M3 - Article
AN - SCOPUS:85047612479
SN - 1754-5692
VL - 11
SP - 1335
EP - 1342
JO - Energy and Environmental Science
JF - Energy and Environmental Science
IS - 5
ER -