TY  - JOUR
AU  - Xiang, Guolei
AU  - Tang, Yan
AU  - Liu, Zigeng
AU  - Zhu, Wei
AU  - Liu, Haitao
AU  - Wang, Jiaou
AU  - Zhong, Guiming
AU  - Li, Jun
AU  - Wang, Xun
TI  - Probing Ligand-Induced Cooperative Orbital Redistribution That Dominates Nanoscale Molecule–Surface Interactions with One-Unit-Thin TiO 2 Nanosheets
JO  - Nano letters
VL  - 18
IS  - 12
SN  - 1530-6992
CY  - Washington, DC
PB  - ACS Publ.
M1  - FZJ-2018-06541
SP  - 7809-7815
PY  - 2018
AB  - Understanding the general electronic principles underlying molecule–surface interactions at the nanoscale is crucial for revealing the processes based on chemisorption, like catalysis, surface ligation, surface fluorescence, etc. However, the electronic mechanisms of how surface states affect and even dominate the properties of nanomaterials have long remained unclear. Here, using one-unit-thin TiO2 nanosheet as a model surface platform, we find that surface ligands can competitively polarize and confine the valence 3d orbitals of surface Ti atoms from delocalized energy band states to localized chemisorption bonds, through probing the surface chemical interaction at the orbital level with near-edge X-ray absorption fine structure (NEXAFS). Such ligand-induced orbital redistributions, which are revealed by combining experimental discoveries, quantum calculations, and theoretical analysis, are cooperative with ligand coverages and can enhance the strength of chemisorption and ligation-induced surface effects on nanomaterials. The model and concept of nanoscale cooperative chemisorption reveal the general physical principle that drives the coverage-dependent ligand-induced surface effects on regulating the electronic structures, surface activity, optical properties, and chemisorption strength of nanomaterials.
LB  - PUB:(DE-HGF)16
C6  - pmid:30407013
UR  - <Go to ISI:>//WOS:000453488800051
DO  - DOI:10.1021/acs.nanolett.8b03572
UR  - https://juser.fz-juelich.de/record/857550
ER  -