TY - JOUR
T1 - Poly(1,4-Diethynylbenzene) Gradient Homojunction with Enhanced Charge Carrier Separation for Photoelectrochemical Water Reduction
AU - Sun, Hanjun
AU - Neumann, Christof
AU - Zhang, Tao
AU - Löffler, Markus
AU - Wolf, André
AU - Hou, Yang
AU - Turchanin, Andrey
AU - Zhang, Jian
AU - Feng, Xinliang
N1 - Publisher Copyright:
© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2019/5/10
Y1 - 2019/5/10
N2 - As appealing photoelectrode materials for photoeletrochemical hydrogen evolution reaction (PEC HER), conjugated polymers still show poor PEC HER performance as a result of their serious recombination of photogenerated electrons and holes. Herein, a novel design of gradient homojunction is demonstrated by controlled copolymerization of 1,4-diethynylbenzene (DEB) and 1,3,5-triethynylbenzene (TEB). The as-built gradient distribution of TEB monomer in poly(1,4-diethynylbenzene) (pDEB) leads to continuous band bending engineering, which constitutes a gradient homojunction. Under AM 1.5G irradiation and in 0.1 m Na 2 SO 4 aqueous solution, the as-fabricated pDEB gradient homojunction exhibits a charge separation efficiency of 0.27% at 0.3 V versus reversible hydrogen electrode (RHE), which is 3.4 and 1.7 times higher than those for pure pDEB and the traditionally designed pDEB homojunction. As a result, the photocurrent of the pDEB gradient homojunction unprecedentedly reaches 55 µA cm −2 at 0.3 V versus RHE, which is much higher than 19 µA cm −2 for pure pDEB, 32 µA cm −2 for the pDEB homojunction, and state-of-the-art organic photocathodes, e.g., g-C 3 N 4 (≈1−32 µA cm −2 ). This work opens up a new window for the design of gradient homojunctions and will advance the exploration of high-performance organic photoelectrodes.
AB - As appealing photoelectrode materials for photoeletrochemical hydrogen evolution reaction (PEC HER), conjugated polymers still show poor PEC HER performance as a result of their serious recombination of photogenerated electrons and holes. Herein, a novel design of gradient homojunction is demonstrated by controlled copolymerization of 1,4-diethynylbenzene (DEB) and 1,3,5-triethynylbenzene (TEB). The as-built gradient distribution of TEB monomer in poly(1,4-diethynylbenzene) (pDEB) leads to continuous band bending engineering, which constitutes a gradient homojunction. Under AM 1.5G irradiation and in 0.1 m Na 2 SO 4 aqueous solution, the as-fabricated pDEB gradient homojunction exhibits a charge separation efficiency of 0.27% at 0.3 V versus reversible hydrogen electrode (RHE), which is 3.4 and 1.7 times higher than those for pure pDEB and the traditionally designed pDEB homojunction. As a result, the photocurrent of the pDEB gradient homojunction unprecedentedly reaches 55 µA cm −2 at 0.3 V versus RHE, which is much higher than 19 µA cm −2 for pure pDEB, 32 µA cm −2 for the pDEB homojunction, and state-of-the-art organic photocathodes, e.g., g-C 3 N 4 (≈1−32 µA cm −2 ). This work opens up a new window for the design of gradient homojunctions and will advance the exploration of high-performance organic photoelectrodes.
KW - conjugated polymers
KW - Glaser polycondensation
KW - gradient homojunctions
KW - hydrogen evolution
KW - photocathodes
UR - http://www.scopus.com/inward/record.url?scp=85063593537&partnerID=8YFLogxK
U2 - 10.1002/adma.201900961
DO - 10.1002/adma.201900961
M3 - 文章
C2 - 30919520
AN - SCOPUS:85063593537
SN - 0935-9648
VL - 31
JO - Advanced Materials
JF - Advanced Materials
IS - 19
M1 - 1900961
ER -