TY - JOUR
T1 - Control of Shell Morphology in p–n Heterostructured Water-Processable Semiconductor Colloids
T2 - Toward Extremely Efficient Charge Separation
AU - Kim, Yu Jin
AU - Schaller, Richard D.
AU - Fry, Harry Christopher
N1 - Funding Information:
This work was performed at the Center for Nanoscale Materials, a U.S. Department of Energy Office (DOE) of Science User Facility and supported by the U.S. Department of Energy, Office of Science, under Contract No. DE-AC02-06CH11357. This research also used resources of the Advanced Photon Source with same project number. Y.J.K. acknowledges support from the Maria Goeppert Mayer Named Fellowship at Argonne National Laboratory. The authors thank Dr. Xiaobing Zuo for fruitful discussions and help with the SAXS analysis.
Publisher Copyright:
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2019/1/11
Y1 - 2019/1/11
N2 - This article describes p–n heterostructured water-borne semiconductor naonoparticles (NPs) with unique surface structures via control of shell morphology. The shell particles, comprising PC60–[6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) composite, having n-type semiconductor characteristics, notably influence the charge carrier behavior in the core–shell NPs. A one- or two-phase methodology based on a PC60 surfactant-water phase and PC61BM n-type semiconductor-organic phase provides highly specific control over the shell structure of the NPs, which promote their superior charge separation ability when combined with poly-3-hexyl-thiophene (P3HT). Moreover, the resulting water-borne NP exhibits shell morphology-dependent carrier quenching and stability, which is characterized via luminescence studies paired with structural analysis. Corresponding to the results, outstanding performances of photovoltaic cells with over 5% efficiency are achieved. The results suggest that the surrounding shell environments, such as the shell structure, and its electronic charge density, are crucial in determining the overall activity of the core–shell p–n heterostructured NPs. Thus, this work provides a new protocol in the current fields of water-based organic semiconductor colloids.
AB - This article describes p–n heterostructured water-borne semiconductor naonoparticles (NPs) with unique surface structures via control of shell morphology. The shell particles, comprising PC60–[6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) composite, having n-type semiconductor characteristics, notably influence the charge carrier behavior in the core–shell NPs. A one- or two-phase methodology based on a PC60 surfactant-water phase and PC61BM n-type semiconductor-organic phase provides highly specific control over the shell structure of the NPs, which promote their superior charge separation ability when combined with poly-3-hexyl-thiophene (P3HT). Moreover, the resulting water-borne NP exhibits shell morphology-dependent carrier quenching and stability, which is characterized via luminescence studies paired with structural analysis. Corresponding to the results, outstanding performances of photovoltaic cells with over 5% efficiency are achieved. The results suggest that the surrounding shell environments, such as the shell structure, and its electronic charge density, are crucial in determining the overall activity of the core–shell p–n heterostructured NPs. Thus, this work provides a new protocol in the current fields of water-based organic semiconductor colloids.
KW - charge separation
KW - organic semiconducting nanoparticles
KW - p–n heterostructure
KW - water-borne colloids
KW - water-processable nanoparticles
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U2 - 10.1002/smll.201803563
DO - 10.1002/smll.201803563
M3 - Article
C2 - 30427577
AN - SCOPUS:85056453684
SN - 1613-6810
VL - 15
JO - Small
JF - Small
IS - 2
M1 - 1803563
ER -