TY - JOUR
T1 - Tunable Chemical Coupling in Two-Dimensional van der Waals Electrostatic Heterostructures
AU - Taniguchi, Takaaki
AU - Li, Shisheng
AU - Nurdiwijayanto, Leanddas
AU - Kobayashi, Yu
AU - Saito, Tetsuki
AU - Miyata, Yasumitsu
AU - Obata, Seiji
AU - Saiki, Koichiro
AU - Yokoi, Hiroyuki
AU - Watanabe, Kenji
AU - Taniguchi, Takashi
AU - Tsukagoshi, Kazuhito
AU - Ebina, Yasuo
AU - Sasaki, Takayoshi
AU - Osada, Minoru
N1 - Funding Information:
This work was supported by JSPS KAKENHI Grant No. JP15H05411, Creation of Life Innovation Materials for Interdisciplinary and International Researcher Development Satellite - MEXT, and Joint Research Program of the Institute of Materials and Systems for Sustainability (IMaSS) - Nagoya University.
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/10/22
Y1 - 2019/10/22
N2 - Heterostructures of two-dimensional (2D) atomic crystals provide fascinating molecular-scale design elements for emergent physical phenomena and functional materials, as integrating distinct monolayers into vertical heterostructures can afford coupling between disparate properties. However, the available examples have been limited to either van der Waals (vdW) or electrostatic (ES) heterostructures that are solely composed of noncharged and charged monolayers, respectively. Here, we propose a "vdW-ES heterostructure" chemical design in which charge-neutral and charged monolayer-building blocks with highly disparate chemical and physical properties are conjugated vertically through asymmetrically charged interfaces. We demonstrate vdW-ES heteroassembly of semiconducting MoS2 and dielectric Ca2Nb3O10 - (CNO) monolayers using an amphipathic molecular starch, resulting in the emergence of trion luminescence observed at the lowest energy among MoS2-related materials, probably due to interfacial confinement effects given by vdW-ES dual interactions. In addition, interface engineering leads to tailored exciton of the vdW/ES heterostructures owing to the pronounced dielectric proximity effects, bringing an intriguing interlayer chemistry to modify 2D materials. Furthermore, the current approach was successfully extended to create a graphene/CNO heterostructure, which verifies the versatility of the preparative method.
AB - Heterostructures of two-dimensional (2D) atomic crystals provide fascinating molecular-scale design elements for emergent physical phenomena and functional materials, as integrating distinct monolayers into vertical heterostructures can afford coupling between disparate properties. However, the available examples have been limited to either van der Waals (vdW) or electrostatic (ES) heterostructures that are solely composed of noncharged and charged monolayers, respectively. Here, we propose a "vdW-ES heterostructure" chemical design in which charge-neutral and charged monolayer-building blocks with highly disparate chemical and physical properties are conjugated vertically through asymmetrically charged interfaces. We demonstrate vdW-ES heteroassembly of semiconducting MoS2 and dielectric Ca2Nb3O10 - (CNO) monolayers using an amphipathic molecular starch, resulting in the emergence of trion luminescence observed at the lowest energy among MoS2-related materials, probably due to interfacial confinement effects given by vdW-ES dual interactions. In addition, interface engineering leads to tailored exciton of the vdW/ES heterostructures owing to the pronounced dielectric proximity effects, bringing an intriguing interlayer chemistry to modify 2D materials. Furthermore, the current approach was successfully extended to create a graphene/CNO heterostructure, which verifies the versatility of the preparative method.
KW - MoS
KW - graphene
KW - heterostructure
KW - interface
KW - metal oxide
KW - nanosheets
KW - two-dimensional materials
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U2 - 10.1021/acsnano.9b04256
DO - 10.1021/acsnano.9b04256
M3 - Article
C2 - 31580052
AN - SCOPUS:85073165637
SN - 1936-0851
VL - 13
SP - 11214
EP - 11223
JO - ACS Nano
JF - ACS Nano
IS - 10
ER -