作者：

Nianyue Zhang^1#, Shuilong Kang^1#, Meng Zhang¹, Sifan You¹, Xiang Hu¹, Guangyuan Feng², Kunal S. Mali², Steven De Feyter², Oleksandr Ivasenko¹*, Lifeng Chi¹*, and Yuan Fang¹*

单位：

¹State Key Laboratory of Bioinspired Interfacial Materials Science, Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, Suzhou 215123, P. R. China

²Department of Chemistry, Division of Molecular Imaging and Photonics, KU Leuven, B-3001 Leuven, Belgium

摘要：

Reversible transitions of surface-adsorbed molecules under external stimuli hold great promise for advancing nanotechnology. Electric fields, in particular, can provide highly localized and tunable forces, enabling on-demand manipulation of molecular assembly and reactivity. However, despite extensive studies, the mechanism governing bias-induced phase transitions in surface-confined systems, particularly those involving neutral molecules like boronic acids, remains ambiguous. Addressing this gap is crucial for the rational design of tunable molecular assemblies. Here, we employ a competitive adsorption strategy to investigate the electric field-mediated switching of multicomponent systems comprising boronic acids and an inert reference compound at the liquid–solid interface. Using scanning tunneling microscopy (STM), we uncovered distinct bias-dependent behaviors, including reversible dynamic exchange and phase transitions. Our findings identify partial ionization as a key mechanism driving the dynamic exchange and structural transformations of boronic acids.

影响因子：

15.8

分区情况：

一区

链接：

https://doi.org/10.1021/acsnano.5c03607