Unleashing the Full Potential of Electrochromic Heterostructured Nickel-Cobalt Phosphate for Optically Active High-Performance Asymmetric Quasi-Solid-State Supercapacitor Devices.

The rational design of hybrid systems that combine capacitor and battery merits is crucial to enable the fabrication of high energy and power density devices. However, the development of such systems remains a significant barrier to overcome. Herein, we report the design of a Ni-Co phosphate (Ni3-xCox(PO4)2·8H2O) nanoplatelet-based system via a facile coprecipitation method at ambient conditions. The nanoplatelets exhibit multicomponent synergy, exceptional charge storage capabilities, rich redox active sites (ameliorating the redox reaction activity), and high ionic diffusion rate/electron transfer kinetics. The designed Ni3-xCox(PO4)2·8H2O offered a respectable gravimetric specific capacity and marvelous capability rate (966 and 595 C g-1 at 1 and 15 A g-1) over the Ni3(PO4)2·8H2O (327.3 C g-1) and Co3(PO4)2·8H2O (68 C g-1) counterparts. Additionally, the nanoplatelets showed enhanced photoactive storage performance with a 9.7% increase in the recorded photocurrent density. Upon integration of Ni3-xCox(PO4)2·8H2O as a positive pole and commercial activated carbon as a negative pole, the constructed hybrid supercapacitor device with PVA@KOH quasi-gel electrolyte exhibits great energy and power densities of 77.7 Wh kg-1 and 15998.54 W kg-1 with remarkable cycling stability of 6000 charging/discharging cycles and prominent Coulombic efficiency of 100%. Interestingly, two assembled devices are capable of glowing a red LED bulb for nearly 180 s. This research paves the way to design and fabricate electroactive species via a facile approach for boosting the design of a plethora of supercapattery devices.

A mesoporous ternary transition metal oxide nanoparticle composite for high-performance asymmetric supercapacitor devices with high specific energy.

We report on the optimized fabrication and electrochemical properties of ternary metal oxide (Ti-Mo-Ni-O) nanoparticles as electrochemical supercapacitor electrode materials. The structural, morphological, and elemental composition of the fabricated Ti-Mo-Ni-O via rapid breakdown anodization are elucidated by field emission scanning electron microscopy, Raman, and photoelectron spectroscopy analyses. The Ti-Mo-Ni-O nanoparticles reveal pseudocapacitive behavior with a specific capacitance of 255.4 F g-1. Moreover, the supercapacitor device Ti-Mo-Ni-O NPs//mesoporous doped-carbon (TMN NPs//MPDC) device exhibited a superior specific energy of 68.47 W h kg-1 with a corresponding power density of 2058 W kg-1. The supercapacitor device shows 100% coulombic efficiency with 96.8% capacitance retention over 11 000 prolonged charge/discharge cycles at 10 A g-1.

Selective electrochemical reduction of CO2 on compositionally variant bimetallic Cu-Zn electrocatalysts derived from scrap brass alloys.

The electrocatalytic reduction of carbon dioxide (CO2RR) into value-added fuels is a promising initiative to overcome the adverse effects of CO2 on climate change. Most electrocatalysts studied, however, overlook the harmful mining practices used to extract these catalysts in pursuit of achieving high-performance. Repurposing scrap metals to use as alternative electrocatalysts would thus hold high privilege even at the compromise of high performance. In this work, we demonstrated the repurposing of scrap brass alloys with different Zn content for the conversion of CO2 into carbon monoxide and formate. The scrap alloys were activated towards CO2RR via simple annealing in air and made more selective towards CO production through galvanic replacement with Ag. Upon galvanic replacement with Ag, the scrap brass-based electrocatalysts showed enhanced current density for CO production with better selectivity towards the formation of CO. The density functional theory (DFT) calculations were used to elucidate the potential mechanism and selectivity of the scrap brass catalysts towards CO2RR. The d-band center in the different brass samples with different Zn content was elucidated.

Innovative nanocomposite formulations for enhancing biogas and biofertilizers production from anaerobic digestion of organic waste.

Herein, the design of nanocomposite (NC) formulations that consist of metal enzyme cofactors, highly conductive carbon materials, DIET activators, to boost AD biogas production from anaerobically incubated cattle manure are investigated and discussed. Three different NC formulations were designed and synthesized: zinc ferrite (ZnFe), ZnFe with 10% carbon nanotubes (ZFCNTs), and zinc ferrite with 10% C76 fullerene (ZFC76). The structure and morphology of the nano-additives were investigated via x-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy dispersive x-ray (EDX), and transmission electron microscopy (TEM). NCs were supplemented to lab-scale biodigesters containing organic slurry. Biogas production was monitored daily and compared to blank biodigesters for 50 days. The maximum methane enhancement was obtained for ZnFe, which promoted methane production to 185.3%. ZFCNTs and ZFC76 showed a positive impact on the hydraulic retention time and enhanced methane production to 162% and 145.9%, respectively compared to the blank reactors.