Wafer scale WS2based ultrafast photosensing and memory computing devices for neuromorphic computing.

Integration of optical sensors with memristors can establish the bridge between photosensing and memory devices for Internet of Things (IoT) based applications. This paper presents the realization of integrated sensing and computing memory (ISCM) devices using tungsten disulfide (WS2) and their application for neuromorphic computing. The ISCM device fabrication process is scalable as microfabrication steps followed on 2″ wafer, ISCM device testing and image classification for neuromorphic computing. The photosensing/memory tests were conducted using electrical and optical stimulations (broadband spectrum). The fabricated photosensing device offers a higher responsivity (8 A W-1), higher detectivity (2.85 × 1011Jones) and fast response speed (80.2/78.3µs) at 950 nm. The memory device has shown a set/reset time of 51.6/73.5µs respectively. Further, the repeatability, stability and reproducibility tests were conducted by stimulating the device with different modulating frequencies. The frequency modulation tests confirm that the ISCM devices are stable and perfect candidate for real-time IoT applications. Moreover, the device's potentiation and depression results were used for image classification with the accuracy of 98.27%. These demonstrated device's test results provide possibilities to fabricate the smart sensors with integrated functionalities.

Nickel(II) complexes with tetra- and pentadentate aminopyridine ligands: synthesis, structure, electrochemistry, and reduction to nickel(I) species.

A series of nickel(II) complexes with polydentate aminopyridine ligands N,N,N'-tris-[2-(2'-pyridyl)ethyl]ethane-1,2-diamine (L1), N,N,N'-tris-[2-(2'-pyridyl)ethyl]-N'-methylethane-1,2-diamine (L2), and N,N'-bis-[2-(2'-pyridyl)ethyl]-N,N'-dimethylethane-1,2-diamine (L3) were synthesized and characterized by elemental analysis and spectroscopic methods. Single-crystal X-ray diffraction studies showed that the Ni(II) ions have five-coordinate square-pyramidal geometry in [NiL2](ClO(4))(2), similar to that previously found in [NiL1](ClO(4))(2) x CH(3)NO(2) (Hoskins, B. F.; Whillans, F. D.J. Chem. Soc., Dalton Trans. 1975, 657), and square-planar geometry in [NiL3](ClO(4))(2). All three nickel(II) complexes are reduced by sodium borohydride or sodium amalgam in organic solvents to nickel(I) species, which were identified by highly anisotropic EPR spectra at 100 K: g(1) = 2.239, g(2) = 2.199, and g(3) = 2.025 for [NiL1](+); g(axially) = 2.324 and g(radially) = 2.079 for [NiL2](+) and [NiL3](+). Cyclic voltammetry of the nickel(II) complexes in acetonitrile exhibited reversible reduction waves at -1.01 V for [NiL1](2+), -0.91 V for [NiL2](2+), and -0.83 V for [NiL3](2+) versus SCE, potentials which are significantly less negative than those of most previously characterized Ni(II) complexes with nitrogen-only donor atoms. Complexes [NiL1](2+) and [NiL2](2+) showed high catalytic activity in the electroreduction of 1,2-trans-dibromocyclohexane to cyclohexene.