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Bimetallic Au@Ag nano-sea urchins (Au@Ag NSUs) functionalized with methimazole were synthesized and combined with paper tips as efficient surface-enhanced Raman scattering (SERS) substrates for ultrasensitive Cr(VI) detection. The redox reaction between methimazole and Cr(VI) ensured the reliability of quantitative Cr(VI) analysis. When droplets were continuously dropped on the tip of the paper, based on the gravity effect, the nanoparticles achieved enrichment at the front end of the tip, which further improved the sensitivity of detection. The detection limit is as low as 0.956 ng L−1, demonstrating its excellent performance in ultrarace Cr(VI) detection. Additionally, the SERS sensor was successfully applied to the detection of Cr(VI) in real water samples, such as lake water and tap water, indicating its wide application potential in environmental monitoring. This study not only provides an efficient and reliable new method for detecting Cr(VI) but also shows the great prospect of paper-based SERS sensors in practical applications. [ABSTRACT FROM AUTHOR]

Water splitting is an energy conversion process of vital importance. The oxygen evolution reaction (OER), as the half-reaction of water splitting, has very slow kinetics due to the complex quaternary electron transfer process involved, which greatly impedes the efficiency of energy conversion. The rational construction and modification of metal–organic frameworks (MOFs) offer a novel alternative for developing efficient OER electrocatalysts. In this study, MOF-74-PA15 with abundant surface defects and high hydrophilicity was successfully in situ constructed by etching MOFs for different reaction times using phytic acid (PA). The etching of PA increases the active area, and improves the hydrophilicity, allowing tighter contact between the material and the electrolyte. As a result, MOF-74-PA15 exhibits the most optimal OER catalytic performance in all the samples. The overpotential is 250 mV in 1 M KOH at 100 mA cm−2, with the lowest Tafel slope (35.59 mV dec−1). Furthermore, MOF-74-PA15 exhibits excellent stability. It maintains stability for 72 hours at a current density of 50 mA cm−2. This study presents a novel and feasible solution for modifying MOFs as electrocatalytic water splitting catalysts. [ABSTRACT FROM AUTHOR]

To address the shortage of fossil energy, the development of affordable and efficient non-precious metal catalysts for oxygen evolution reaction (OER) from electrocatalytic water splitting is still a crucial challenge. Herein, the bimetallic NiFe metal–organic frameworks (MOFs) are synthesized by hydrothermal and electro-deposition. Benefiting from the synergistic effect of Fe and Ni, the catalyst demonstrates extraordinary activity, which exhibits favorable OER catalytic activity in 1 M KOH solution with an overpotential of 206 mV at 10 mA cm−2. Meanwhile, the obtained NiFe-NDC presents promising stability in the 20 h test at 50 mA cm−2. [ABSTRACT FROM AUTHOR]

The efficiency and reproducibility of perovskite solar cells (PSCs) are significantly influenced by the purity of lead iodide (PbI2) in the raw materials used. Pb(OH)I has been identified as the primary impurity generated from PbI2 in water-based synthesis. Consequently, a comprehensive investigation into the impact of Pb(OH)I impurities on film and device performance is essential. In this study, PbI2, with varying stoichiometries, was synthesized to examine the effects of different Pb(OH)I levels on perovskite device performance. The characterization results revealed that even trace amounts of Pb(OH)I impede the formation of precursor prenucleation clusters. These impurities also increase the energy barrier of the α-phase and facilitate the transition of the intermediate phase to the δ-phase. These effects result in poor perovskite film morphology and sub-optimal photovoltaic device performance. To address these issues, a cost-effective method for preparing high-stoichiometry PbI2 was developed. The formation of Pb(OH)I was effectively inhibited through several strategies: adjusting solution pH and temperature, modifying material addition order, simplifying the precipitation–recrystallization process, and introducing H3PO2 as an additive. These modifications enabled the one-step synthesis of high-purity PbI2. PSCs prepared using this newly synthesized high-stoichiometry PbI2 demonstrated photovoltaic performance comparable to those fabricated with commercial PbI2 (purity ≥ 99.999%). Our novel method offers a cost-effective alternative for synthesizing high-stoichiometry PbI2, thereby providing a viable option for the production of high-performance PSCs. [ABSTRACT FROM AUTHOR]

Developing efficient and economical catalysts is essential for water splitting. The application of MOF catalysts in water splitting is limited by poor conductivity; however, the introduction of conductive TMS could enhance their activity. Herein, novel composite Fe9S10/Fe-MOF/NF-2 was constructed by introducing dendritic Fe9S10 onto the surface of a 2D ultrathin Fe-MOF. Composite catalysts elaborately utilize the structural and chemical advantages of MOF and TMS while improving the deficiencies of monomers through the combination. Owing to the optimal structure, the hybrid catalyst Fe9S10/Fe-MOF/NF-2 displayed better catalytic performance than bare Fe-MOFs and Fe9S10, with low overpotentials of 202 and 216 mV at 10 mA cm−2 in alkaline solution and simulated seawater, respectively. This work provides an innovative approach to modify MOFs as electrocatalysts for OER. [ABSTRACT FROM AUTHOR]

The use of photocatalysts based on semiconductor heterostructures for hydrogen evolution is a prospective tactic for converting solar energy. Herein, visible-light-responsive three-dimensional core–shell CoSe2/ZnIn2S4 heterostructures were successfully fabricated via in situ growth of ZnIn2S4 ultrathin nanosheets on spherical CoSe2. Without any noble metal co-catalysts, the as-prepared CoSe2/ZnIn2S4 composite achieved attractive photocatalytic hydrogen evolution activity under visible light illumination. Optimal CoSe2/ZnIn2S4 achieved a hydrogen evolution rate of 2199 μmol g−1 h−1, which was 7 times higher than that of pristine ZnIn2S4 and even exceeded that of ZnIn2S4 loaded with platinum. In this distinctive core–shell heterostructure, the presence of CoSe2 could considerably improve the ability to harvest light, quicken the charge transfer kinetics, and avoid the agglomeration of ZnIn2S4 nanosheets. Meanwhile, the experimental results demonstrated that the strong interaction between CoSe2 and ZnIn2S4 at the compact interface could appropriately boost the photogenerated electron–hole pair migration and relieve charge recombination, thus improving photocatalytic hydrogen evolution activity. This work has bright prospects in constructing noble-metal-free core–shell heterostructures for solar energy conversion. [ABSTRACT FROM AUTHOR]

Chemical mechanism (CM)-related surface-enhanced Raman spectroscopy (SERS) has received tremendous interest due to its exceptional stability and excellent uniformity. Nevertheless, there remains a demand for ingenious methodologies for promoting effective charge transfer (CT) to improve SERS sensitivity further. Herein, a band structure engineered W18O49/g-C3N4 heterostructure (WCN) was first employed as a CM-based SERS substrate with remarkable enhancement and sensitivity. To investigate the Raman enhancement properties of the substrate, malachite green (MG) was employed as the Raman probe with the excitation of a 633 nm laser. The WCN substrate exhibits a Raman enhancement factor (EF) of 2.6 × 107, achieving a limit of detection (LOD) of 1.9 × 10−10 M for MG. The outstanding Raman amplification behavior can be attributed to the heterojunction-induced efficient CT process, energy band matching resonance due to minor doping with g-C3N4 serving as a band gap modifier, and improved photo-induced charge transfer (PICT) efficiency via the oxygen vacancies in the W18O49 units. Additionally, a flexible SERS substrate based on WCN was constructed using a vacuum filtration method and utilized to detect prohibited pharmaceutical residues on fish skin. The integration of this WCN and a nylon membrane not only preserves the Raman activity of the WCN for sensitive detection but also endows the Raman substrate with high flexibility and good mechanical durability, making it a potential candidate for in situ detection in particular environments. [ABSTRACT FROM AUTHOR]

High-performance SERS chips via self-assembled hollow Ag octahedra on PDMS were employed to achieve the sensitive identification and detection of antibiotic residues. The developed SERS chips were successfully applied in the detection of ciprofloxacin (CIP), amoxicillin (AMX) and cefazolin (CZL) in wastewater and tap water samples, as well as enrofloxacin (ENR) in milk, demonstrating the sensitive determination of antibiotics in the real environment. From this perspective, these SERS chips are expected to expand the on spot sensitive detection and identification field of antibiotic residues. [ABSTRACT FROM AUTHOR]

It is widely acknowledged that interface engineering strategies can significantly enhance the activity of catalysts. In this study, we developed a CoMoP nanoarray directly grown in situ on a nickel foam (NF) substrate, with the interface structure formed through the electrodeposition of MnOxHy. The resulting heterostructure MnOxHy/CoMoP/NF exhibited remarkable hydrogen evolution reaction (HER) activity, achieving overpotentials as low as 61 and 138 mV at 10 and 100 mA cm−2, respectively. Moreover, MnOxHy/CoMoP/NF demonstrated efficient oxygen evolution reaction (OER) activity with an overpotential of 330 mV at 100 mA cm−2. Remarkably, MnOxHy/CoMoP/NF maintained its catalytic properties and structural integrity even after working continuously for 20 h facilitating the HER at 10 mA cm−2 and the OER at 100 mA cm−2. The Tafel slopes of the HER and OER were determined to be as small as 14 and 55 mV dec−1, respectively, confirming that the coupled interface conferred fast reaction kinetics on the catalyst. When applied in overall water splitting, MnOxHy/CoMoP/NF delivered a voltage of 1.91 V at 100 mA cm−2 with excellent stability. This study demonstrated the feasibility of utilizing a simple electrodeposition technique to fabricate a heterogeneous structure with bifunctional catalytic activity, establishing a solid foundation for diverse industrial applications. [ABSTRACT FROM AUTHOR]