Fostering Charge Carrier Transport and Absorber Growth Properties in CZTSSe Thin Films with an ALD-SnO2 Capping Layer.

The present study demonstrates that precursor passivation is an effective approach for improving the crystallization process and controlling the detrimental defect density in high-efficiency Cu2ZnSn(S,Se)4 (CZTSSe) thin films. It is achieved by applying the atomic layer deposition (ALD) of the tin oxide (ALD-SnO2) capping layer onto the precursor (Cu-Zn-Sn) thin films. The ALD-SnO2 capping layer was observed to facilitate the homogeneous growth of crystalline grains and mitigate defects prior to sulfo-selenization in CZTSSe thin films. Particularly, the CuZn and SnZn defects and deep defects associated with Sn were effectively mitigated due to the reduction of Sn2+ and the increase in Sn4+ levels in the kesterite CZTSSe film after introducing ALD-SnO2 on the precursor films. Subsequently, devices integrating the ALD-SnO2 layer exhibited significantly reduced recombination and efficient charge transport at the heterojunction interface and within the bulk CZTSSe absorber bulk properties. Finally, the CZTSSe device showed improved power conversion efficiency (PCE) from 8.46% to 10.1%. The incorporation of ALD-SnO2 revealed reduced defect sites, grain boundaries, and surface roughness, improving the performance. This study offers a systematic examination of the correlation between the incorporation of the ALD-SnO2 layer and the improved PCE of CZTSSe thin film solar cells (TFSCs), in addition to innovative approaches for improving absorber quality and defect control to advance the performance of kesterite CZTSSe devices.

Electrochemical Detection of a Breast Cancer Biomarker with an Amine-Functionalized Nanocomposite Pt-Fe3O4-MWCNTs-NH2 as a Signal-Amplifying Label.

We report an ultrasensitive sandwich-type electrochemical immunosensor to detect the breast cancer biomarker CA 15-3. Amine-functionalized composite of reduced graphene oxide and Fe3O4 nanoparticles (MRGO-NH2) was used as an electrochemical sensing platform material to modify the electrodes. The nanocomposite comprising Pt and Fe3O4 nanoparticles (NPs) anchored on multiwalled carbon nanotubes (Pt-Fe3O4-MWCNTs-NH2) was utilized as a pseudoenzymatic signal-amplifying label. Compared to reduced graphene oxide, the composite MRGO-NH2 platform material demonstrated a higher electrochemical signal. In the Pt-Fe3O4-MWCNTs-NH2 label, multiwalled carbon nanotubes provided the substratum to anchor abundant catalytic Pt and Fe3O4 NPs. The nanocomposites were thoroughly characterized using transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, and X-ray photoelectron spectroscopy. An electroanalytical study and prevalidation of the immunosensor was carried out. The immunosensor exhibited exceptional capabilities in detecting CA 15-3, offering a wider linear range of 0.0005-100 U mL-1 and a lower detection limit of 0.00008 U mL-1. Moreover, the designed immunosensor showed good specificity, reproducibility, and acceptable stability. The sensor was successfully applied to analyze samples from breast cancer patients, yielding reliable results.

Improving the Device Performance of CZTSSe Thin-Film Solar Cells via Indium Doping.

Cation incorporation emerges as a promising approach for improving the performance of the kesterite Cu2ZnSn(S,Se)4 (CZTSSe) device. Herein, we report indium (In) doping using the chemical bath deposition (CBD) technique to enhance the optoelectronic properties of CZTSSe thin-film solar cells (TFSCs). To incorporate a small amount of the In element into the CZTSSe absorber thin films, an ultrathin (<10 nm) layer of In2S3 is deposited on soft-annealed precursor (Zn-Sn-Cu) thin films prior to the sulfo-selenization process. The successful doping of In improved crystal growth and promoted the formation of larger grains. Furthermore, the CZTSSe TFSCs fabricated with In doping exhibited improved device performance. In particular, the In-CZTSSe-2-based device showed an improved power conversion efficiency (PCE) of 9.53%, open-circuit voltage (Voc) of 486 mV, and fill factor (FF) of 61% compared to the undoped device. Moreover, the small amount of In incorporated into the CZTSSe absorber demonstrated reduced nonradiative recombination, improved carrier separation, and enhanced carrier transport properties. This study suggests a simple and effective way to incorporate In to achieve high efficiency and low Voc loss.

In Situ Fabrication of Nickel-Iron Oxalate Catalysts for Electrochemical Water Oxidation at High Current Densities.

Ni-Fe-based electrode materials are promising candidates for the oxygen evolution reaction (OER). The synergy between Fe and Ni atoms is crucial in modulating the electronic structure of the active site to enhance electrochemical performance. Herein, a simple chemical immersion technique was used to grow Ni-Fe oxalate nanowires directly on a porous nickel foam substrate. The as-prepared Ni-Fe oxalate electrode exhibited an excellent electrochemical performance of the OER with ultralow overpotentials of 210 and 230 mV to reach 50 and 100 mA cm-2 current densities, respectively, in a 1 M KOH aqueous solution. The excellent OER performance of this Ni-Fe oxalate electrode can be attributed to its bimetallic composition and nanowire structure, which leads to an efficient ionic diffusion, high electronic conductivity, and fast electron transfer. The overall analysis indicates a suitable approach for designing electrocatalysts applicable in energy conversion.

A Facile Process for Partial Ag Substitution in Kesterite Cu2ZnSn(S,Se)4 Solar Cells Enabling a Device Efficiency of over 12.

A cation substitution in Cu2ZnSn(S,Se)4 (CZTSSe) offers a viable strategy to reduce the open-circuit voltage (Voc)-deficit by altering the characteristics of band-tail states, antisite defects, and related defect clusters. Herein, we report a facile single process, i.e., simply introducing a thin Ag layer on a metallic precursor, to effectively improve the device characteristics and performances in kesterite (Agx,Cu1-x)2ZnSn(Sy,Se1-y)4 (ACZTSSe) solar cells. Probing into the relationship between the external quantum efficiency derivative (dEQE/dλ) and device performances revealed the Voc-deficit characteristics in the ACZTSSe solar cells as a function of Cu and Ag contents. The fabricated champion ACZTSSe solar cell device showed an efficiency of 12.07% and a record low Voc-deficit of 561 mV. Thorough investigations into the mechanism underpinning the improved performance in the ACZTSSe device further revealed the improved band-tailing characteristic, effective minority carrier lifetime, and diode factors as well as reduced antisite defects and related defect clusters as compared to the CZTSSe device. This study demonstrates the feasibility of effectively suppressing antisite defects, related defect clusters, and band-tailing characteristics by simply introducing a thin Ag layer on a metallic precursor in the kesterite solar cells, which in turn effectively reduces the Voc-deficit.

Achieving Low VOC-deficit Characteristics in Cu2ZnSn(S,Se)4 Solar Cells through Improved Carrier Separation.

Kesterite-based thin-film solar cells (TFSCs) have recently gained significant attention in the photovoltaic (PV) sector for their elemental earth abundance and low toxicity. An inclusive study from the past reveals basic knowledge about the grain boundary (GB) and grain interior (GI) interface. However, the compositional dependency of the surface potential within GBs and GIs remains unclear. The present work provides insights into the surface potential of the bulk and GB interfaces. The tin (Sn) composition is sensitive to the absorber morphology, and therefore, it significantly impacts absorber and device properties. The absorber morphology improves with the formation of larger grains as the Sn content increases. Additionally, the presence of Sn(S,Se)2 and increased [ZnCu + VCu] A-type defect cluster density are observed, validated through Raman analysis. The secondary ion mass spectroscopy analysis reveals the altered distribution of sulfur (S) and sodium (Na) with higher near-surface accumulation. The synergistic outcome of the increased density of defects and the accumulation of S near the interface provides a larger GB and GI difference and expedites carrier separation improvement. Consequently, at an optimum compositional ratio of Cu/(Zn+Sn) = ∼0.6, the power conversion efficiency (PCE) is significantly improved from 6.42 to 11.04% with a record open-circuit voltage (VOC) deficit of 537 mV.

Cost-effective and efficient water and urea oxidation catalysis using nickel-iron oxyhydroxide nanosheets synthesized by an ultrafast method.

The synthesis of earth-abundant, low-cost, and stable electrocatalysts with high efficiency in the oxygen evolution reaction (OER) is a necessary requirement for improving the effectiveness of electrochemical water splitting approach. To date, expensive electrode materials and time-consuming synthesis procedures have generally been used for the electrocatalysts applied in water splitting, which limits their efficiency. Herein, nickel-iron oxyhydroxide nanosheets are fabricated by a scalable and ultrafast (requiring only 5 s) wet chemical strategy on a nickel foam substrate. The experimental results indicate that compared to recently reported catalysts, the prepared nickel-iron oxyhydroxide electrode has a high number of active sites and low reaction barrier, enabling efficient OER catalysis in an alkaline electrolyte. In particular, the prepared nickel-iron oxyhydroxide electrode requires an ultralow overpotential of 230 mV to reach a current density of 50 mA cm-2, with excellent long-term stability for 75 h. Moreover, the nickel-iron oxyhydroxide also performs well towards the electrocatalytic urea oxidation reaction (UEOR), with a very low potential of 1.38 and 1.41 V vs RHE (reversible hydrogen electrode) to reach 50 and 100 mA cm-2 current density in 1 M KOH with 0.33 M urea electrolyte. This ultrafast synthesis approach can be extended to prepare electrocatalysts used for other electrochemical reactions.

Trifunctional layered electrodeposited nickel iron hydroxide electrocatalyst with enhanced performance towards the oxidation of water, urea and hydrazine.

In recent years, low-cost, non-noble metal-based and stable catalysts have gained attention for the development of clean energy devices. Additionally, the synthesis of materials that can exhibit more than one electrocatalytic reaction is notable. In this work, stepwise electrodeposited nickel-iron hydroxide nanoarrays are investigated as anode electrocatalysts with enhanced performance towards the oxidation of water, urea, and hydrazine. The stepwise electrodeposited nickel-iron hydroxide (NiFe(OH)2-SD/NF) electrodes show excellent electrocatalytic activity and stability for the oxygen evolution reaction (OER) with a low potential of 1.45 V (vs RHE) at a current density of 10 mA cm-2. These electrodes further display excellent catalytic activity towards the urea oxidation reaction (UOR) and hydrazine oxidation reaction (HzOR) with potentials lower than 1.32 V (vs RHE) and 0.06 V (vs RHE), respectively. Owing to synergistic effects, a porous structure for mass transport leads to excellent electrocatalytic performance. This non-precious-metal nickel-iron hydroxide, prepared by a simple synthesis approach, is promising for hybrid water electrolysis applications and the development of environmentally friendly clean energy reactions.

Towards highly efficient and low-cost oxygen evolution reaction electrocatalysts: An effective method of electronic waste management by utilizing waste Cu cable wires.

Currently, electronic waste (e-waste) is the world's most challenging and rapidly growing problem in the waste stream. To develop an alternative way to use e-waste (waste copper (Cu) wires) to accelerate the oxygen evolution reaction (OER) of water electrolysis, the waste Cu wires are used as a low-cost current collector. We demonstrate a simple electrodeposition process to deposit nickel-iron hydroxide (NiFe LDH) nanosheets on self-supported copper hydroxide (Cu(OH)2/Cu) nanowires grown via chemical-oxidation on waste Cu wire. Benefiting from the efficient electron transport, high mass activity, and surface area this electrocatalyst exhibits an efficient OER performance with a low overpotential of 275 mV and 390 mV at 20 and 100 mA cm-2 respectively, with excellent stability. This work provides a promising pathway to recycle e-waste into value-added resources in various energy conversion applications.