A hybrid composite of rGO/TiO2 as a double layer electrode with improved capacitance performance

Reduced graphene oxide (rGO) has unique properties that can revolutionize the performance of the functional devices. rGO hybrids can be designed with transition metal oxides for improved energy storage applications. Herein, a hybrid composite of conductive rGO with titanium dioxide, designed by a simple hydrothermal method, is reported to demonstrate a high double layer capacitance in aqueous electrolyte systems. The mesoporous structure of the composite provides short ion diffusion pathways and the resultant capacitance of the material is 334 F g⁻¹ with ~77% capacitance retention after 7000 charge-discharge cycles.     

In situ electrodeposition of nickel cobalt selenides on FTO as an efficient counter electrode for dye-sensitized solar cells

Construction of transition metal selenides with high electrocatalytic performance is of significant importance, but it is still a challenge to develop the corresponding counter electrodes (CEs) by an electrodeposition technique. In the present work, nickel cobalt selenide (Ni_xCo_ySe) films are prepared in situ on fluorine-doped tin oxide (FTO) glasses through a potential reversal electrodeposition technique. The morphology and electronic structure of Ni_xCo_ySe films can be tuned by controlling the Ni/Co molar ratio in electroplating solution. Specially, Ni_xCo_ySe-6 film (the Ni/Co molar ratio of 1:1) with the optimized interaction between the Ni and Co elements displays numerous particles composed of sheets attached with nanocrystals, resulting in the more electrocatalytic active sites. Benefiting from the unique morphology and optimized synergistic effect, Ni_xCo_ySe-6 CE exhibits superior electrocatalytic activity for the triiodide reduction. Then, the dye-sensitized solar cell (DSC) fabricated by Ni_xCo_ySe-6 CE has demonstrated a power conversion efficiency (PCE) over 7.40%, which is higher than that of platinum (Pt)-based device (6.32%). Furthermore, Ni_xCo_ySe-6 array CE is also prepared by using polystyrene array as template. The PCE of the DSC with Ni_xCo_ySe-6 array CE reaches its maximum value of 7.64% and 20.9% larger than that of Pt-based device.     

Low‐cost dye‐sensitized solar cells with ball‐milled tellurium‐doped graphene as counter electrodes and a natural sensitizer dye

This paper presents a facile and economic development of dye‐sensitized solar cells using a nonprecious counter electrode made from ball‐milled tellurium‐doped graphene (Te‐Gr) and a natural sensitizer extracted from Calotropis gigantea leaves. The prepared materials were characterized using various techniques, such as Raman spectroscopy, X‐ray diffraction (XRD), atomic force microscopy (AFM), impedance spectroscopy, and scanning electron microscopy with built‐in energy‐dispersive X‐ray spectroscopy (SEM with EDS). The electrochemical activity of the produced counter electrodes and the impedance of the fabricated cells were examined and discussed to devise plans for future enhancement of cell performance. A clear pattern of improvement was found when using cost‐effective Te‐Gr relative to the costly platinum counter electrodes, especially when compared with cells employing another natural sensitizer. The results show approximately 51% enhancement over chlorophyll‐based cells made from spinach, where the added advantage in our approach is the utilization of an abundant plant extract with little nutritional appeal.     

A spiral shaped regenerative microfluidic fuel cell with Ni‐C based porous electrodes

Microchannel geometry, electrode surface area, and better fuel utilization are important aspects of the performance of a microfluidic fuel cell (MFC). In this communication, a membraneless spiral‐shaped MFC fabricated with Ni as anode and C as a cathode supported over a porous filter paper substrate is presented. Vanadium oxychloride and dilute sulfuric acid solutions are used as fuel and electrolyte, respectively, in this fuel cell system. The device generates a maximum open‐circuit voltage of ~1.2 V, while the maximum energy density and current density generated from the fuel cell are ~10 mW cm^?2 and ~51 mA cm^?2, respectively. The cumulative energy density generated from the device after five cycles are measured as ~200 mW after regeneration of the fuel by applying external voltage. The spiral design of the fuel cell enables improved fuel utilization, rapid diffusive transport of ions, and in‐situ regeneration of the fuel. The present self‐standing spiral‐shaped MFC will eliminate the challenges associated with two inlet membrane‐less fuel cells and has the potential to scale up for commercial application in portable energy generation.     

Splashing-Assisted Femtosecond Laser-Activated Metal Deposition for Mold- and Mask-Free Fabrication of Robust Microstructured Electrodes for Flexible Pressure Sensors (Small 24/2023)

Flexible pressure sensors play an indispensable role in flexible electronics. Microstructures on flexible electrodes have been proven to be effective in improving the sensitivity of pressure sensors. However, it remains a challenge to develop such microstructured flexible electrodes in a convenient way. Inspired by splashed particles from laser processing, herein, a method for customizing microstructured flexible electrodes by femtosecond laser-activated metal deposition is proposed. It takes advantage of the catalyzing particles scattered during femtosecond laser ablation and is particularly suitable for moldless, maskless, and low-cost fabrication of microstructured metal layers on polydimethylsiloxane (PDMS). Robust bonding at the PDMS/Cu interface is evidenced by the scotch tape test and the duration test over 10 000 bending cycles. Benefiting from the firm interface, the developed flexible capacitive pressure sensor with microstructured electrodes presents several conspicuous features, including a sensitivity (0.22 kPa⁻¹) 73 times higher than the one using flat Cu electrodes, ultralow detection limit (<1 Pa), rapid response/recovery time (4.2/5.3 ms), and excellent stability. Moreover, the proposed method, inheriting the merits of laser direct writing, is capable of fabricating a pressure sensor array in a maskless manner for spatial pressure mapping.     

Hydroxyapatite-Derived Heterogeneous Ru-Ru2P Electrocatalyst and Environmentally-Friendly Membrane Electrode toward Efficient Alkaline Electrolyzer

Alkaline membrane water electrolysis is a promising production technology, and advanced electrocatalyst and membrane electrode design have always been the core technology. Herein, an ion-exchange method and an environmentally friendly in situ green phosphating strategy are successively employed to fabricate Ru-Ru₂P heterogeneous nanoparticles by using hydroxyapatite (HAP) as a phosphorus source, which is an exceptionally active electrocatalyst for hydrogen evolution reaction (HER). Density functional theory calculation results reveal that strong electronic redistribution occurs at the heterointerface of Ru-Ru₂P, which modulates the electronic structure to achieve an optimized hydrogen adsorption strength. The obtained Ru-Ru₂P possesses excellent HER performance (24 mV at 10 mA cm⁻²) and robust stability (1000 mA cm⁻² for 120 h) in alkaline media. Furthermore, an environmentally friendly membrane electrode with a sandwich structure is assembled by HAP nanowires as an alkaline membrane, Ru-Ru₂P as a cathodic catalyst, and NiFe-LDH as an anodic catalyst, respectively. The voltage of (−) Ru-Ru₂P || NiFe-LDH/CNTs (+) (1.53 V at 10 mA cm⁻²) is lower than that of (−) 20 wt% Pt/C || RuO₂ (+) (1.60 V at 10 mA cm⁻²) for overall water splitting. Overall, the studies not only design an efficient catalyst but also provide a new route to achieve a high-stability electrolyzer for industrial H₂ production.     

Pt‐Free Counter Electrode for Dye‐Sensitized Solar Cells with High Efficiency

Dye‐sensitized solar cells (DSSCs) have attracted widespread attention in recent years as potential cost‐effective alternatives to silicon‐based and thin‐film solar cells. Within typical DSSCs, the counter electrode (CE) is vital to collect electrons from the external circuit and catalyze the I₃^? reduction in the electrolyte. Careful design of the CEs can improve the catalytic activity and chemical stability associated with the liquid redox electrolyte used in most cells. In this Progress Report, advances made by our groups in the development of CEs for DSSCs are reviewed, highlighting important contributions that promise low‐cost, efficient, and robust DSSC systems. Specifically, we focus on the design of novel Pt‐free CE catalytic materials, including design ideas, fabrication approaches, characterization techniques, first‐principle density functional theory (DFT) calculations, ab‐initio Car‐Parrinello molecular dynamics (CPMD) simulations, and stability evaluations, that serve as practical alternatives to conventional noble metal Pt electrodes. We stress the merits and demerits of well‐designed Pt‐free CEs, such as carbon materials, conductive polymers, transition metal compounds (TMCs) and their corresponding hybrids. Also, the prospects and challenges of alternative Pt catalysts for their applications in new‐type DSSCs and other catalytic fields are discussed.