To utilize continuous ultralow intensity signals from oxide synaptic transistors as artificial synapses that mimic human visual perception, we propose strategic oxide channels that optimally utilize their advantageous functions by stacking two oxide semiconductors with different conductivities. The bottom amorphous indium–gallium–zinc oxide (a-IGZO) layer with a relatively low conductivity was designed for an extremely low initial postsynaptic current (PSCi) by achieving full depletion at a low negative gate voltage, and the stacked top amorphous indium–zinc oxide (a-IZO) layer improved the amplitude of the synaptic current and memory retention owing to the enhancement in the persistent photoconductivity characteristics. We demonstrated an excellent photonic synapse thin-film transistor (TFT) with a precise synaptic weight change even in the range of ultralow light intensity by adapting this stacking IGZO/IZO channel. The proposed device exhibited distinct ∆PSC values of 3.1 and 18.1 nA under ultralow ultraviolet light (350 nm, 50 ms) of 1.6 and 8.0 μW/cm2. In addition, while the lowest light input exhibited short-term plasticity characteristics similar to the “volatile-like” behavior of the human brain with a current recovery close to the initial value, the increase in light intensity caused long-term plasticity characteristics, thus achieving synaptic memory transition in the IGZO/IZO TFTs.

Applications of abundant seawater in electrochemical energy conversion are constrained due to the sluggish oxygen evolution reaction and the corrosive chlorine oxidation reaction. Hence, it is imperative to develop an efficient anodic reaction alternative suitable for coupling with the cathodic counterpart. Due to a low thermodynamic oxidation potential, hydrazine oxidation reaction (HzOR) offers a unique pathway to overcome these challenges. Herein, spontaneously in situ reduced atomic scale Pd surface‐confined to electrochemically prepared layered Co(OH)2 on carbon cloth is synthesized. This study reveals the hydrazine and Pd‐dependent morphological evolution of Co(OH)2 and its Pd hybrids into nanoparticulate form. Unlike various layered double hydroxides, Pd integrated Co(OH)2 benefits from the contribution of Co(OH)2 as an active HzOR catalyst and the reductive support to host Pd, resulting in synergistically improved performances. Mass activities of Pd in alkaline and alkaline saline electrolyte are 11.24 and 9.83 A mgPd−1 at 200 mV, respectively, corresponding to the highest HzOR activities among noble metals. The optimized Pd hybrid demonstrates ≈6.5 times the current density relative to PtC (14.91 mA cm−2 at 200 mV) in alkaline saline water with hydrazine. These findings would be beneficial to realize high overpotential anodic alternatives and reduce over‐dependence on freshwater for electrocatalysis.

Hydrazine Electrooxidation In article number 2300639, Swagotom Sarker, Ji Hoon Choi, Hyung Koun Cho, and co‐workers reveal the hydrazine and Pd‐dependent morphological evolution of Co(OH)2 and its Pd hybrids into nanoparticulate form. They uncover that the ultra‐low scale Pd confined on the Co(OH)2 surface is a competent catalyst to synergistically enhance hydrazine oxidation reaction (HzOR) in both alkaline and alkaline saline electrolytes as an alternative to the conventional oxygen evolution reaction (OER) and the corrosive chlorine oxidation reaction (ClOR).