Jialin Zhang

Gap States Assisted MoO3 Nanobelt Photodetector with Wide Spectrum Response

Molybdenum oxides have been widely investigated for their broad applications ranging from electronics to energy storage. Photodetectors based on molybdenum trioxide (MoO3), however, were seldom reported owing to their low conductivity and weak photoresponse. Herein we report a photodetector based on single MoO3 nanobelt with wide visible spectrum response by introducing substantial gap states via H2 annealing. The pristine MoO3 nanobelt possessed low electrical conductance and no photoresponse for nearly all visible lights. The H2 annealing can significantly improve the conductance of MoO3 nanobelt, and result in a good photodetector with wide visible spectrum response. Under illumination of 680 nm light, the photodetector exhibited high responsivity of ~56 A/W and external quantum efficiency of ~10200%. As corroborated by in situ ultraviolet photoelectron spectroscopy and X-ray photoelectron spectroscopy investigations, such strong wide spectrum photoresponse arises from the largely enriched gap states in the MoO3 nanobelt after H2 annealing.

Energy Level Realignment in Weakly Interacting Donor–Acceptor Binary Molecular Networks

Understanding the effect of intermolecular and molecule-substrate interactions on molecular electronic states is key to revealing the energy level alignment mechanism at organic-organic heterojunctions or organic-inorganic interfaces. In this paper, we investigate the energy level alignment mechanism in weakly interacting donor-acceptor binary molecular superstructures, comprising copper hexadecafluorophthalocyanine (F16CuPc) intermixed with copper phthalocyanine (CuPc), or manganese phthalocynine (MnPc) on graphite. The molecular electronic structures have been systematically studied by in situ ultraviolet photoelectron spectroscopy (UPS) and low-temperature scanning tunneling microscopy/spectroscopy (LT-STM/STS) experiments and corroborated by density functional theory (DFT) calculations. As demonstrated by the UPS and LT-STM/STS measurements, the observed unusual energy level realignment (i.e., a large downward shift in donor HOMO level and a corresponding small upward shift in acceptor HOMO level) in the CuPc-F16CuPc binary superstructures originates from the balance between intermolecular and molecule-substrate interactions. The enhanced intermolecular interactions through the hydrogen bonding between neighboring CuPc and F16CuPc can stabilize the binary superstructures and modify the local molecular electronic states. The obvious molecular energy level shift was explained by gap-state-mediated interfacial charge transfer.

Elementary Process for CVD Graphene on Cu(110): Size-selective Carbon Clusters

Revealing the graphene growth mechanism at the atomic-scale is of great importance for achieving high quality graphene. However, the lack of direct experimental observation and density functional theory (DFT) verification hinders a comprehensive understanding of the structure of the carbon clusters and evolution of the graphene growth on surface. Here, we report an in-situ low-temperature scanning tunneling microscopy (LT-STM) study of the elementary process of chemical vapor deposition (CVD) graphene growth via thermal decomposition of methane on Cu(110), including the formation of monodispersed carbon clusters at the initial stage, the graphene nucleation and the ripening of graphene islands to form continuous graphene film. STM measurement, supported by DFT calculations, suggests that the carbon clusters on the surface are C2H5. It is found that graphene layers can be joined by different domains, with a relative misorientation of 30°. These graphene layers can be decoupled from Cu(110) through low temperature thermal cycling.

Single molecule tunneling spectroscopy investigation of reversibly switched dipolar vanadyl phthalocyanine on graphite

We report a spatially resolved scanning tunneling spectroscopy (STS) investigation of reversibly switchable dipolar vanadyl phthalocyanine (VOPc) on graphite by using low temperature scanning tunneling microscopy. VOPc molecule can be switched between O-up and O-down configurations by changing the polarity of the pulse voltage applied to the tip, actuated by the inelastic tunneling electrons. The spatially resolved STS measurements allow the identification of the electronic structures of VOPc with different dipole orientation. The present approach provides geometry images and electronic characterization of a molecular switch on surface spontaneously.