TY - JOUR
T1 - Composites of platinum particles embedded into poly(6-cyanoindole)/poly(styrenesulfonic acid) for methanol oxidation
AU - Kuo, Chung Wen
AU - Lu, Chih Wei
AU - Chang, Jeng Kuei
AU - Chen, Ho Rei
AU - Wu, Tzi Yi
N1 - Publisher Copyright:
© 2020 Hydrogen Energy Publications LLC
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020
Y1 - 2020
N2 - Poly(6-cyanoindole) (P(CnId)) is blended with poly(styrenesulfonic acid) via doping periods of 1, 10, 20, and 30 s to obtain P(CnId)–1PSS, P(CnId)–10PSS, P(CnId)–20PSS, and P(CnId)–30PSS electrodes, respectively. FT-IR studies have revealed that P(CnId) is doped with PSS. Pt particles can be doped into P(CnId)–1PSS, P(CnId)–10PSS, P(CnId)–20PSS, and P(CnId)–30PSS by chronocoulometry (0.15 C) using electrodeposition to acquire P(CnId)–1PSS–Pt, P(CnId)–10PSS–Pt, P(CnId)–20PSS–Pt, and P(CnId)–30PSS–Pt films, respectively. For comparative purposes, in this study, Pt particles were deposited into P(CnId) under the same conditions. Scanning electron microscopy (SEM) characterization revealed that platinum distributes more uniformly into the as-prepared P(CnId)–10PSS films. The anodic peak currents could be clearly observed to reach the saturation point at a methanol concentration larger than 0.8 M. A large electrocatalytic current towards methanol oxidation (27 mA cm−2 mg−1) was noticed in P(CnId)–10PSS–Pt electrodes in comparison to P(CnId)–Pt without PSS (6.3 mA cm−2 mg−1) at +0.86 V (vs. RHE), indicating that the P(CnId)–10PSS–Pt electrode reveals potential applicability as an electrocatalyst support.
AB - Poly(6-cyanoindole) (P(CnId)) is blended with poly(styrenesulfonic acid) via doping periods of 1, 10, 20, and 30 s to obtain P(CnId)–1PSS, P(CnId)–10PSS, P(CnId)–20PSS, and P(CnId)–30PSS electrodes, respectively. FT-IR studies have revealed that P(CnId) is doped with PSS. Pt particles can be doped into P(CnId)–1PSS, P(CnId)–10PSS, P(CnId)–20PSS, and P(CnId)–30PSS by chronocoulometry (0.15 C) using electrodeposition to acquire P(CnId)–1PSS–Pt, P(CnId)–10PSS–Pt, P(CnId)–20PSS–Pt, and P(CnId)–30PSS–Pt films, respectively. For comparative purposes, in this study, Pt particles were deposited into P(CnId) under the same conditions. Scanning electron microscopy (SEM) characterization revealed that platinum distributes more uniformly into the as-prepared P(CnId)–10PSS films. The anodic peak currents could be clearly observed to reach the saturation point at a methanol concentration larger than 0.8 M. A large electrocatalytic current towards methanol oxidation (27 mA cm−2 mg−1) was noticed in P(CnId)–10PSS–Pt electrodes in comparison to P(CnId)–Pt without PSS (6.3 mA cm−2 mg−1) at +0.86 V (vs. RHE), indicating that the P(CnId)–10PSS–Pt electrode reveals potential applicability as an electrocatalyst support.
KW - Electrocatalyst
KW - Platinum
KW - Poly(6-cyanoindole)
KW - Poly(styrenesulfonic acid)
KW - Support material
UR - http://www.scopus.com/inward/record.url?scp=85095737210&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2020.10.131
DO - 10.1016/j.ijhydene.2020.10.131
M3 - Article
AN - SCOPUS:85095737210
SN - 0360-3199
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
ER -