Abstract:Due to the efficient photocarrier separation and collection coming from their distinctive band structures, superlattice nanowires (NWs) have great potential as active materials for high-performance optoelectronic devices. In this work, InGaZnO NWs with superlattice structure and controllable stoichiometry are obtained by ambient-pressure chemical vapor deposition. Along the NW axial direction, perfect alternately stacking of InGaO(ZnO) 4 + blocks and InO 2 − layers is observed to form a periodic layered struct… Show more
“…As shown in Figure h,i, the I – t (current–time) curve, with the UV light of 1.25 mW cm –2 switching on and off every 10 s, the stoichiometric GaS shows very stable and consistent performance with a sharp edge, indicating instant response. The response time is less than 66 ms (Figure S6, Supporting Information), which is two to three orders less than other visible‐light blind UV photodetectors (Table S1, Supporting Information) . However, the photocurrent of GaS 0.87 decreased drastically as soon as the light was on, and continued with every switching on of the light, dropping to only half of its starting values after only a total of 110 s exposure.…”
A chemical vapor deposition method is developed for thickness‐controlled (one to four layers), uniform, and continuous films of both defective gallium(II) sulfide (GaS): GaS0.87 and stoichiometric GaS. The unique degradation mechanism of GaS0.87 with X‐ray photoelectron spectroscopy and annular dark‐field scanning transmission electron microscopy is studied, and it is found that the poor stability and weak optical signal from GaS are strongly related to photo‐induced oxidation at defects. An enhanced stability of the stoichiometric GaS is demonstrated under laser and strong UV light, and by controlling defects in GaS, the photoresponse range can be changed from vis‐to‐UV to UV‐discriminating. The stoichiometric GaS is suitable for large‐scale, UV‐sensitive, high‐performance photodetector arrays for information encoding under large vis‐light noise, with short response time (<66 ms), excellent UV photoresponsivity (4.7 A W–1 for trilayer GaS), and 26‐times increase of signal‐to‐noise ratio compared with small‐bandgap 2D semiconductors. By comprehensive characterizations from atomic‐scale structures to large‐scale device performances in 2D semiconductors, the study provides insights into the role of defects, the importance of neglected material‐quality control, and how to enhance device performance, and both layer‐controlled defective GaS0.87 and stoichiometric GaS prove to be promising platforms for study of novel phenomena and new applications.
“…As shown in Figure h,i, the I – t (current–time) curve, with the UV light of 1.25 mW cm –2 switching on and off every 10 s, the stoichiometric GaS shows very stable and consistent performance with a sharp edge, indicating instant response. The response time is less than 66 ms (Figure S6, Supporting Information), which is two to three orders less than other visible‐light blind UV photodetectors (Table S1, Supporting Information) . However, the photocurrent of GaS 0.87 decreased drastically as soon as the light was on, and continued with every switching on of the light, dropping to only half of its starting values after only a total of 110 s exposure.…”
A chemical vapor deposition method is developed for thickness‐controlled (one to four layers), uniform, and continuous films of both defective gallium(II) sulfide (GaS): GaS0.87 and stoichiometric GaS. The unique degradation mechanism of GaS0.87 with X‐ray photoelectron spectroscopy and annular dark‐field scanning transmission electron microscopy is studied, and it is found that the poor stability and weak optical signal from GaS are strongly related to photo‐induced oxidation at defects. An enhanced stability of the stoichiometric GaS is demonstrated under laser and strong UV light, and by controlling defects in GaS, the photoresponse range can be changed from vis‐to‐UV to UV‐discriminating. The stoichiometric GaS is suitable for large‐scale, UV‐sensitive, high‐performance photodetector arrays for information encoding under large vis‐light noise, with short response time (<66 ms), excellent UV photoresponsivity (4.7 A W–1 for trilayer GaS), and 26‐times increase of signal‐to‐noise ratio compared with small‐bandgap 2D semiconductors. By comprehensive characterizations from atomic‐scale structures to large‐scale device performances in 2D semiconductors, the study provides insights into the role of defects, the importance of neglected material‐quality control, and how to enhance device performance, and both layer‐controlled defective GaS0.87 and stoichiometric GaS prove to be promising platforms for study of novel phenomena and new applications.
“…2,5 Other noteworthy features of this system and, in particular, in the case of In 2-x Ga x O 3 (ZnO) m nanowires, are the improvement of the thermoelectric figure of merit by 2.5 orders of magnitude, in comparison to undoped ZnO nanowires, and the excellent sensitivity to ultraviolet light irradiation as photodetectors. [21][22][23] In the case of Al 3+ doping, Košir et al 24 reported the improvement of the thermoelectric properties caused by the small addition of Al 3+ in Zn 5 In 2 O 8 ceramics. On the other hand, only few studies about the influence of In 3+ substitution in the luminescent properties of IMZOs (M=Ga, Al) performed on microwires have been reported so far.…”
The
effect of In3+ substitution by Ga3+ or
Al3+ on the structure and luminescent properties of Zn7In2–x
M
x
O10 (M = Ga or Al; 0 ≤ x ≤ 1) oxides has been investigated by means of high spatial
resolution X-ray spectroscopy and high-angle annular dark-field images,
combined with magic angle spinning nuclear magnetic resonance spectroscopy.
Local structural variations have been identified for the Al- and Ga-doped
samples through the analysis of atomically resolved chemical maps
and the identification of their structural environment within the
wurtzite lattice. In3+ is distributed in a zig-zag modulation,
while Al3+ and Ga3+ are located in a flat distribution
at the center of the wurtzite block. Density functional theory calculations
provide unambiguous evidence for the preferential flat location of
Ga3+ and Al3+ associated with the different
strains introduced in the structure as a result of their ionic radii.
The characterization of the photoluminescence response reveals the
appearance of new radiative recombination pathways for the doped materials
because of the presence of new defect levels in the band gap of the
Zn7In2O10 structure.
“…[50] In these cases, the interaction of simultaneous light pulses with adsorbed and bulk oxygen in the surface depletion region play a key role in regulating the NW conductance, that is, the synaptic weight. [9,51] In a recent work, both volatile and non-volatile resistive switching have been achieved in Ag-contacted ZnO nanowire devices, mainly enabled by the atomic Ag diffusion along the NW (Figure 2f,g), which well emulate the ion migration dynamics in biological synapses. [35] With detailed investigation of the memristive mechanism in the Ag-ZnO system, the underlying electrochemical fundamentals of filament formation/dissolution highlight the Ag + /Ag redox reactions and transport characteristics on the crystalline NW surface.…”
Section: D Quantum Materials For Artificial Synapsesmentioning
Neuromorphic in-memory computing systems, comprising artificial synapses and neurons, can overcome the energy inefficiency and throughput limitation of today's von Neumann computing architecture. Recently, powered by the unique properties of quantum materials, for example, high mobility, outstanding sensitivity, and strong quantum effect, researchers have built quantum artificial synapses to mimic the biological ones. These quantum electronic/photonic synapses can precisely define their conductance state (or synaptic weight) for emulating synaptic behaviors, which shows bionic performance unreachable by other conventional materials. In this review, the significant achievements in quantum artificial synapses are summarized. First, potential quantum materials used in artificial synapses are discussed with particular attention to quantum dots, nanowires, layered materials, and quasi-2DEG interfaces. Then, the major quantum effects that are utilized in quantum artificial synapses, for example, Josephson effect, quantum tunneling, and spin memory, are reviewed. In addition to the discussion on a single synaptic device, the macroscale integration into artificial visual systems and artificial nerve networks are also highlighted. Finally, the associated future research trends and target applications are also discussed.
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