Tao Cai-Ping, Jiang Chen-Chen, Wang Ya-Hao, Zheng Ju-Fang, Shao Yong, Zhou Xiao-Shun
Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Institute of Physical Chemistry, Zhejiang Normal University, Jinhua 321004, China.
J Phys Chem Lett. 2020 Dec 3;11(23):10023-10028. doi: 10.1021/acs.jpclett.0c03010. Epub 2020 Nov 12.
Bronsted acid and base interactions are a cornerstone of chemistry describing a wide range of chemical phenomena. However, probing such interaction at the solid-liquid interface to extract the elementary and intrinsic information at a single-molecule level remains a big challenge. Herein, we employ an STM break junction (STM-BJ) technique to investigate the acid-base chemistry of carboxylic acid-based molecules at a Au (111) model surface and propose a prototype of a single-molecule pH sensor for the first time. The single-molecule measurements in different environmental conditions verify that the formation probability of molecular junctions is determined by the populations of deprotonated -COO form in a self-assembled monolayer. Furthermore, the variation of the intensity of the conductance peaks (i.e., junction-forming probability) with the pH of the bulk solution fits well to the Henderson-Hasselbalch type equation. From the equation, a good linear relation is found between the degree of dissociation of the immobilized -COOH group and the environmental pH, providing a feasible way to design chemicals and biosensors and a detector at the single-molecule scale.
布朗斯特酸碱相互作用是描述广泛化学现象的化学基石。然而,在固液界面探测这种相互作用以在单分子水平提取基本和内在信息仍然是一个巨大挑战。在此,我们采用扫描隧道显微镜断结(STM-BJ)技术研究基于羧酸的分子在金(111)模型表面的酸碱化学,并首次提出单分子pH传感器的原型。在不同环境条件下的单分子测量证实,分子结的形成概率由自组装单分子层中去质子化的-COO形式的数量决定。此外,电导峰强度(即结形成概率)随本体溶液pH值的变化与亨德森-哈塞尔巴尔赫型方程拟合良好。从该方程中发现,固定化的-COOH基团的解离度与环境pH值之间存在良好的线性关系,为在单分子尺度设计化学品、生物传感器和探测器提供了一种可行的方法。