Structure-Independent Conductance of Thiophene-Based Single-Stacking Junctions.

Intermolecular charge transport is crucial in π-conjugated materials but the experimental investigation remained challenging. Here, we show that charge transport through intermolecular and intramolecular paths in single-molecule and single-stacking thiophene junctions could be investigated using the mechanically controllable break junction (MCBJ) technique. We found that intermolecular charge transport ability through different single-stacking junctions is approximately independent of molecular structures, which contrasts with the strong length dependence of conductance in single-molecule junctions with the same building blocks, and the dominant charge transport path of molecules with two anchors transits from intramolecular to intermolecular paths when the conjugation pattern increased. The increase of conjugation further leads to higher binding probabilities due to the variation in binding energies supported by density functional theory (DFT) calculations. Our results demonstrate that intermolecular charge transport is not only the limiting step but also provides the efficient and dominate charge transport path at the single-molecule scale

Room-temperature quantum interference in single perovskite quantum dot junctions.

The studies of quantum interference effects through bulk perovskite materials at the Ångstrom scale still remain as a major challenge. Herein, we provide the observation of room-temperature quantum interference effects in metal halide perovskite quantum dots (QDs) using the mechanically controllable break junction technique. Single-QD conductance measurements reveal that there are multiple conductance peaks for the CH3NH3PbBr3 and CH3NH3PbBr2.15Cl0.85 QDs, whose displacement distributions match the lattice constant of QDs, suggesting that the gold electrodes slide through different lattice sites of the QD via Au-halogen coupling. We also observe a distinct conductance ’jump’ at the end of the sliding process, which is further evidence that quantum interference effects dominate charge transport in these single-QD junctions. This conductance ’jump’ is also confirmed by our theoretical calculations utilizing density functional theory combined with quantum transport theory. Our measurements and theory create a pathway to exploit quantum interference effects in quantum-controlled perovskite materials

Room-temperature quantum interference in single perovskite quantum dot junctions

钙钛矿材料由于其高量子产率、载流子迁移率和独特的光致发光特性而在光电材料领域存在诸多潜在的重要应用。研究钙钛矿材料在纳米尺度下电荷输运的独特尺寸效应对钙钛矿光电器件的设计和开发具有重要的指导意义。洪文晶教授课题组基于机械可控裂结技术自主研发了具有皮米级位移调控灵敏度和飞安级电学测量精度的精密科学仪器，对南开大学李跃龙副教授团队合成的钙钛矿量子点进行了深入表征，研究工作成功将量子干涉的研究体系拓展至在光电领域具有重要应用的钙钛矿材料领域，为未来制备基于量子干涉效应的新型钙钛矿器件提供了一种全新的思路。 这一跨学科国际合作研究工作是在化学化工学院洪文晶教授、英国Lancaster 大学物理系Colin J. Lambert教授以及南开大学电子信息与光电工程学院李跃龙副教授的共同指导下完成的。化工系硕士研究生郑海宁、Lancaster University大学Songjun Hou博士、南开大学硕士研究生辛晨光为论文第一作者。博士后林禄春，博士研究生谭志冰、郑珏婷，硕士研究生蒋枫、张珑漪，本科生何文翔、李庆民等参与了论文的研究工作。刘俊扬特任副研究员、师佳副教授和萨本栋微纳米研究院杨扬副教授也参与了部分指导工作。The studies of quantum interference effects through bulk perovskite materials at the Ångstrom scale still remain as a major challenge. Herein, we provide the observation of roomtemperature quantum interference effects in metal halide perovskite quantum dots (QDs) using the mechanically controllable break junction technique. Single-QD conductance measurements reveal that there are multiple conductance peaks for the CH3NH3PbBr3 and CH3NH3PbBr2.15Cl0.85 QDs, whose displacement distributions match the lattice constant of QDs, suggesting that the gold electrodes slide through different lattice sites of the QD via Auhalogen coupling. We also observe a distinct conductance ‘jump’ at the end of the sliding process, which is further evidence that quantum interference effects dominate charge transport in these single-QD junctions. This conductance ‘jump’ is also confirmed by our theoretical calculations utilizing density functional theory combined with quantum transport theory. Our measurements and theory create a pathway to exploit quantum interference effects in quantum-controlled perovskite materials.This work was supported by the National Key R&D Program of China (2017YFA0204902, 2014DFE60170, 2018YFB1500105), the National Natural Science Foundation of China (Nos. 21673195, 21503179, 21490573, 61674084, 61874167), the Open Fund of the Key Laboratory of Optical Information Science & Technology (Nankai University) of China, the Fundamental Research Funds for the Central Universities of China (63181321, 63191414, 96173224), and the 111 Project (B16027), the Tianjin Natural Science Foundation (17JCYBJC41400), FET Open project 767187—QuIET, the EU project BAC-TO-FUEL and the UK EPSRC projects EP/N017188/1, EP/M014452/1. 该工作得到国家重点研发计划课题（2017YFA0204902）、国家自然科学基金（21673195、21503179、21490573）、厦门大学“人工智能分析引擎”双一流重大专项等项目的资助，也得到了固体表面物理化学国家重点实验室、能源材料化学协同创新中心的支持

Room-temperature quantum interference in single perovskite quantum dot junctions

The studies of quantum interference effects through bulk perovskite materials at the Ångstrom scale still remain as a major challenge. Herein, we provide the observation of room-temperature quantum interference effects in metal halide perovskite quantum dots (QDs) using the mechanically controllable break junction technique. Single-QD conductance measurements reveal that there are multiple conductance peaks for the CH3NH3PbBr3 and CH3NH3PbBr2.15Cl0.85 QDs, whose displacement distributions match the lattice constant of QDs, suggesting that the gold electrodes slide through different lattice sites of the QD via Au-halogen coupling. We also observe a distinct conductance ‘jump’ at the end of the sliding process, which is further evidence that quantum interference effects dominate charge transport in these single-QD junctions. This conductance ‘jump’ is also confirmed by our theoretical calculations utilizing density functional theory combined with quantum transport theory. Our measurements and theory create a pathway to exploit quantum interference effects in quantum-controlled perovskite materials

Static-Errorless Rotor Position Estimation Method Based on Linear Extended State Observer for IPMSM Sensorless Drives

This article presents a static-errorless rotor position estimation method based on the linear extended state observer (LESO) for interior permanent magnet synchronous motor (IPMSM) drives. Two second-order LESOs are utilized to estimate the α-β axis back-EMFs. A third-order LESO is incorporated into the quadrature phase-locked loop (QPLL) to achieve a high robustness of position tracking against external disturbance. In addition, considering that the nonideal back-EMF will bring DC and harmonic fluctuation errors to the estimated position, an enhanced LESO-based QPLL with static-errorless rotor position estimation is proposed. On the one hand, the DC position esti mation error caused by the phase lag of the back-EMF estimator is analyzed and compensated. On the other hand, to suppress the position harmonic fluctuations induced from the nonsinusoidal back-EMFs, a second-order generalize integrator (SOGI) is embedded in the feedforward path of the LESO-based QPLL. The experimental results on the 1.0 kW IPMSM drive platform show that, compared to the conventional method, the proposed method can achieve better position estimation performance both in steady-state operation and in transient-state operation

Improved Linear Active Disturbance Rejection Control for IPMSM Drives Considering Load Inertia Mismatch

This article presents an improved linear active disturbance rejection control (LADRC) method for interior permanent magnet synchronous motor (IPMSM) drives. The proposed method adopts a dual LADRC structure. The outer LADRC-based speed regulator adopts position feedback instead of speed feedback so that the low-pass filter for speed calculation can be eliminated. The inner LADRC-based current regulator incorporates a maximum torque per ampere (MTPA) operation scheme to improve the torque output capacity and the efficiency of the motor. In addition, considering the variation of load inertia in real applications, a systematic modelling and analysis on the effect of inertia mismatch is presented. To enhance the robustness of the drive system to inertia mismatch, an inertia identification method is proposed, in which the inertia information is extracted from the estimated disturbance of speed loop LESO. Finally, the effectiveness of the proposed method is verified on a 1.0-kW IPMSM drive platform

Community Participation and Residents’ Support for Tourism Development in Ancient Villages: The Mediating Role of Perceptions of Conflicts in the Tourism Community

As increasing numbers of tourists have begun to visit ancient villages, conflicts between tourism development and residents have become one of the main challenges to the sustainable development of the tourism community. This research explores the relationship between community participation and residents’ support for tourism development in an ancient village. This study surveyed 249 indigenous residents living in Whampoa Village, Guangzhou, China. The findings show that community participation in tourism development has a positive influence on residents’ support for tourism development, and this relationship is mediated by the perceptions of conflicts in the tourism community. This study contributes a new theoretical perspective and practical implications for the sustainable development of ancient villages

Single-Molecule Charge Transport Modulation Induced by Steric Effects of Side Alkyl Chains

Experimental investigation of the side chain effects on intramolecular charge transport in π-conjugated molecules is essential, but remains challenging. Herein, the dependence of intra-molecular conductance on the nature of branching alkyl chains is investigated through a combination of the scanning tunneling microscope break junction (STM-BJ) technique and density functional theory. Three thiophene-flanked diketopyrrolopyrrole (DPP) derivatives with different branching alkyl chains (isopentane, 3-methylheptane , and 9-methylnonadecane) are used with phenylthiomethyl groups as the anchoring groups. The results of single-molecule conductance measurements show that as the alkyl chain becomes longer, the torsional angles between the aromatic rings increase due to steric crowding, and therefore, the molecular conductance of DPP decreases due to reduction in conjugation. Both theoretical simulations and 1 H NMR spectra demonstrate that the planarity of the DPPs is directly reduced after introducing longer branching alkyl chains, which leads to the reduced conductance. This work indicates that the effect of insulating side chain on single-molecule conductance cannot be neglected, which should be considered for the design of future organic semiconducting materials

Enhanced π–π Stacking between Dipole-Bearing Single Molecules Revealed by Conductance Measurement

Dipoles are widely involved in π-π interactions and are central to many chemical and biological functions, but their influence on the strength of π-π interactions remains unclear. Here, we report a study of π-π interaction between azulene-based, polar single molecules and between naphthalene-based, nonpolar single molecules. By performing scanning tunneling microscopy break junction measurements of single-molecule conductance, we show that the π-stacked dimers formed by the azulene-based, polar aromatic structures feature higher electrical conductivity and mechanical stability than those formed by the naphthalene-based, nonpolar molecules. Mechanical control of π-π interactions in both rotational and translational motion reveals a sensitive dependence of the stacking strength on relative alignment between the dipoles. The antiparallel alignment of the dipoles was found to be the optimal stacking configuration that underpins the observed enhancement of π-π stacking between azulene-based single molecules. Density functional theory calculations further explained the observed enhancement of stacking strength and the corresponding charge transport efficiency. Our experimental and theoretical results show that the antiparallel alignment of the dipole moments significantly enhances the electronic coupling and mechanical stability of π-π stacking. In addition, in the formation of single-molecule junctions, the azulene group was experimentally and theoretically proved to form a Au−π contact with electrodes with high charge transport efficiency. This paper provides evidence and interpretation of the role of dipoles in π-π interactions at the single-molecule level and offers new insights into potential applications in supramolecular devices