Hongqian Sang

Motivated by the quest for experimental procedures capable of controlled manipulation of single atoms on surfaces, we set up a computational strategy that explores the cyclical vertical manipulation of a broad set of single atoms on the GaAs(110) surface. First-principles simulations of atomic force microscope tip–sample interactions were performed considering families of GaAs and Au-terminated tip apexes with varying crystalline termination. We identified a subset of tips capable of both picking up and depositing an adatom (Ga, As, Al, and Au) any number of times via a modify–restore cycle that “resets” the apex of the scanning probe to its original structure at the end of each cycle. Manipulation becomes successful within a certain window of lateral and vertical tip distances that are observed to be different for extracting and depositing each atom. A practical experimental protocol of special utility for potential cyclical manipulation of single atoms on a nonmetallic surface is proposed.

Planar-type perovskite solar cells (p-PSCs) based on SnO₂ have garnered further attention due to their simple and low-temperature fabrication. Improving the critical properties of the electron transport layer (ETL) is an effective way to enhance the performance of p-PSC devices. Here, a brand-new method is developed to relieve the contact recombination caused by the rough fluorine-doped tin oxide (FTO) surface and further boosts the electrical concentration of the ETL. A SnO₂–ethylene diamine tetraacetic acid (EDTA) acylamide compound (SEAC) with hydrogen bond-induced adjustable cluster size is reported for the first time. The rational choice of the SEAC cluster size is the key for obtaining the smooth interfacial morphology of the ETL on the rugged FTO substrate. In addition, the energy band gap decreases with the increasing cluster size, and consequently, results in improved electrical conductivity of the SEAC. The upshifted Fermi energy level leads to higher electron concentration, which is an important physical quantity of the ETL. The PSC devices based on the optimized SEAC achieve an improved power conversion efficiency of 21.29% with negligible J–V hysteresis due to significantly enhanced electron transport and reduced contact charge recombination at the ETL/perovskite interface. In general, this paper comes up with a unique strategy to improve the quality of the SnO₂-based ETL.

The redox states of oxygen species on the surface of TiO₂ can be altered by electron tunneling by varying the applied bias voltage of an atomic force microscope tip. However, tunneling is stochastic in nature and typically requires ultra-low temperatures to obtain statistically significant data. Here, we use a highly sensitive fast atomic force microscopy setup to study redox transitions of oxygen atoms on a TiO₂ surface, in the form of reactive oxygen species and single-atom quantum dots, at 78 K. The fast and highly sensitive nature of our experimental setup enables a statistically necessary amount of data to be collected without having to resort to ultra-low temperatures. This enabled us to study multiple dots and provide insight into the electronic structure and correlation between the oxygen species, which are inaccessible by standard atomic force microscopy. We show that single-atom quantum dots exist in two charge states with drastically different conductance, with one being conducting and the other non-conducting.

Transition and dissociation of adsorbed O ₂ with three different configurations are directly observed at 78 K by atomic force microscopy.

Recent advances in scanning probe microscopy on surface enable not only direct observation of molecular structures but also local probe reactions, in which unstable short‐lived products have been synthesized and analyzed. Now, an endergonic reaction to synthesize a single Sondheimer–Wong diyne from 6,13‐dibromopentaleno[1,2‐b:4,5‐b′]dinaphthalene by local probe chemistry on a ultra‐thin film of NaCl formed on a Cu(111) surface at 4.3 K is presented. The structures of the precursor, two intermediates, and the final product were directly identified by the differential conductance imaging with a CO functionalized tip. DFT calculations revealed that the multiple‐step reaction, being endergonic overall, is facilitated by temporal charging and discharging of the molecule placed in the nanometric junction between the Cu tip and the Cu substrate underneath the ultra‐thin NaCl film. This local probe reaction expands possibilities to synthesize nanocarbon materials in a bottom‐up manner.

Recent advances in scanning probe microscopy on surface enable not only direct observation of molecular structures but also local probe reactions, in which unstable short‐lived products have been synthesized and analyzed. Now, an endergonic reaction to synthesize a single Sondheimer–Wong diyne from 6,13‐dibromopentaleno[1,2‐b:4,5‐b′]dinaphthalene by local probe chemistry on a ultra‐thin film of NaCl formed on a Cu(111) surface at 4.3 K is presented. The structures of the precursor, two intermediates, and the final product were directly identified by the differential conductance imaging with a CO functionalized tip. DFT calculations revealed that the multiple‐step reaction, being endergonic overall, is facilitated by temporal charging and discharging of the molecule placed in the nanometric junction between the Cu tip and the Cu substrate underneath the ultra‐thin NaCl film. This local probe reaction expands possibilities to synthesize nanocarbon materials in a bottom‐up manner.

The long time dynamics of molecular ratchets on a 1D periodic potential energy surface (PES) subjected to an external stimulus is studied using the rate equation method. The PES consisting of repeated waveforms made of two peaks is considered as an example of a spatially symmetric or asymmetric PES. This PES may, for example, correspond to diffusion of a bipedal molecule that moves along an atomic track via an inchworm walk mechanism [Raval et al., Angew. Chem., Int. Ed., 2015, 54, 7101]. Generalisation to a PES consisting of an arbitrary number of peaks of various heights is straightforward. Assuming the validity of the transition state theory (TST) for the calculation of the transition rates between neighbouring potential wells, the probability of occupying each type of potential well on the PES is obtained analytically, and then the net current for the molecules to move preferentially in a particular direction under application of external fields over a long time is derived. Note that different to methods based on solving numerically the corresponding Fokker–Plank equation, our method is entirely analytical in the limit of weak external fields. The results of the analytical calculations are compared with the exact numerical solution of the derived rate equations. The following external stimuli are considered: constant, sinusoidal and shifted sinusoidal fields due to either a spatially uniform thermal gradient or an electrostatic field. The possible applications of the method for extracting energy from the Brownian motion under load and separating molecules of different chiralities on the surface are also discussed.