Mo Metal Research Articles

Electronic interaction between d electron-poor and d electron-rich transition metal ions promoted the CO2 capture performance of calcium-based adsorbent

The investigation of intrinsic principles for the more precise design CaO adsorbent with excellent CO2 capture performance by doping metal oxides is of great significance, but has not yet been explored. Herein, we address the critical challenge by systematical evaluation on a series of magnetic bimetallic oxides doped calcium-based adsorbents from the perspective of electronic interaction between d electron-poor and d electron-rich transition metal ions promoting the CO2 capture performance. The Mn, Co, Mo and Ni metal ions with varied d-electron numbers are doped into calcium-based adsorbent, and the results show that the introduction of magnetic bimetallic oxides with d electron-poor and d electron-rich transition metal ions into CaO at the same time can significantly promote the stability of CO2 capture. Taking the (Mn-Co)-codoped samples as an example, the relationship of d electron-poor and d electron-rich transition metal ions synergistic interaction and promoted CO2 adsorption performance is elucidated. The loose flake nanostructures favor the diffusion of CO2 inside the particles, and the uniform distribution of each component effectively ensures the double-exchange interactions. The generation of more oxygen vacancies significantly improves the CO2 affinity for the calcium-based sample. Furthermore, the results of kinetic analysis reveal that the synergistic interaction can reduce the apparent activation energy of carbonation reaction. These insights into the systematical regulation of the double-exchange interaction are expected to provide guidance for the relatively more precise design of the calcium-based adsorbent with high performance of CO2 adsorption.

Comprehensive extraction of V, Ni and Mo from black shale via selective leaching oxidation process

Black shale is one of the most representative sources of vanadium, nickel and molybdenum in China. Due to the poor endowment of minerals in black shale, V, Ni, Mo and other metals complex co-associated endowment state, extraction is difficult and long-term unused, resulting in a significant waste of resources. In this paper, it is shown that V, Ni and Mo can be obtained from black shale by a stepwise oxidation leaching process. In a first leaching process, V and Ni are effectively leached simultaneously. Mo is left in the residue. The leaching efficiency of V, Ni and Mo was 86.81%, 89.19% and 5.80% respectively under the leaching conditions of 35wt.% H2SO4, 4wt.% CaF2, 1.2:1 liquid to solid ratio (L/kg), 95℃ and 8h. The residue was then leached twice. The leaching efficiency of molybdenum was 91.10% under the leaching conditions of 25wt.% H2SO4, 8wt.% NaClO3, 1.5:1 liquid to solid ratio (L/kg), 45℃ and 7h. V2O5 products have been successfully prepared, the purity of V2O5 reaches 98.34%. A stepwise oxidation leaching method has been proposed to separate the vanadium, nickel and molybdenum in the leaching process. Vanadium, nickel and molybdenum can be effectively extracted from the black shale by the stepwise oxidation leaching process to maximize the utilization of the resources.

Innovative Design of anode materials for Li-ion batteries: Bismuth oxide/sodium bismuth molybdate nanocomposites

Novel bismuth oxide/sodium bismuth molybdate nanocomposites (NCs), Bi2O3@NaBi(MoO4)2, were developed successfully via simple methods. Advanced analyses revealed that the NCs were composed of Bi2O3 and NaBi(MoO4)2 particles at the nanoscale, below 10 nm, in a combination of amorphous and crystalline forms. In this work, these NCs were utilized as lithium-ion battery anode materials for the first time, demonstrating exceptional electrochemical performances, including high capacity, superior capacity retention, high coulombic efficiency, excellent rate capacity, and pseudo-capacitance behavior. For instance, Bi2O3@NaBi(MoO4)2 NCs prepared at 1 h and 3 h of reaction time delivered a reversible charge capacity of 1052 and 1034 mAh g−1 after 200 cycles at current densities of 0.1 A g−1 with a capacity retention of 110 and 129 %, respectively. Notably, all the NCs anodes exhibited an excellent initial coulombic efficiency of above 80 %. Materials characterizations and electrochemical analysis revealed that the improved electrochemical properties of the NCs were attributed to their unique architectures, which featured nanostructures, molybdate components, and a small amount of amorphous phase. In addition, the significant capacity increase could be due to the electrochemical milling effect, the in situ formation of metallic particles, and the role of Mo metal in the NCs anodes as the catalysts for Li2O decomposition during cycling. It concluded that Bi2O3@NaBi(MoO4)2 NCs have great potential as advanced anodes for Li-ion storages.

Liquid metal embrittlement and fracture behavior of three Mo metals in liquid lead-bismuth eutectic

In this work, liquid metal embrittlement (LME) and the related fracture behavior of Mo, TZM and Mo-14Re were assessed in oxygen-saturated and -depleted LBE at 350°C by means of slow strain rate tensile (SSRT) tests. Neither tensile mechanical property data nor fractographic micrographs show strong evidence of LME. Nevertheless, the observation of deep secondary cracking at the fiber-like grain boundaries of Mo and Mo-14Re tested in LBE suggests occurrence of grain boundary wetting (GBW). Moreover, oxidation-assisted crack initiation and propagation were also identified. Both fracture modes may be a concern when Mo metals with a fiber-like grain structure are used in high-oxygen LBE environment.

Influence of different metal-modified Beta zeolites on the liquid-phase isomerisation of xylene and reaction mechanisms

PX is a very important chemical raw material. There are few studies on the liquid-phase isomerisation of xylene. Here, a series of Beta catalysts with different metal modifications were prepared and tested for many characterisations. The reaction performance of the catalysts was evaluated in the liquid-phase MX isomerisation reaction. The results show that the loading of La, Ce, Mo,Fe and Mg metals decreases the specific surface area and acid content of Beta zeolite. Among them, Mo has a strong interaction with the skeleton Al atoms in Beta. The side reactions of MX isomerisation were inhibited by metal loading, and the selectivity of PX and OX was improved. The effect of Mo content on the liquid-phase isomerisation of MX was further investigated. The selectivity of PX can be improved by appropriate Mo content. This is related to the reaction mechanism of the liquid-phase isomerisation of MX at mainly low temperatures. The acidic site density of B and L acids on the catalyst surface was successfully modulated by Mo loading. At 260 °C, the conversion of MX over Mo/Beta catalyst was about 33 % and the PX yield was 12.83 %. In addition, based on the results of liquid-phase isomerisation of MX, OX and PX, the transformation relationship between the three isomers was investigated.

Reaction pathways for the formation of complex fluorides revealed by in situ synchrotron X-ray diffraction

This study investigated the reaction between LiF, Mo metal, and CuF2 as a solid-state fluorine source to form a complex fluoride, tetragonal trirutile (TR)-type Li2MoF6, in an Ni metal tube by in situ synchrotron X-ray diffraction (SXRD) experiments. As a result, two formation pathways of TR-type Li2MoF6 were identified: one involving a reaction among intermediate phases, i.e., MoF3, and an unknown Mo-containing fluoride, and the starting materials, i.e., LiF, Mo, and CuF2, the other involving a direct reaction between LiF, Mo, and CuF2. The combination of in situ SXRD with differential scanning calorimetry (DSC) revealed that the direct reaction was facilitated by the presence of the liquid phase of LiF-CuF2. Further, the first-order phase transition of Li2MoF6 with a great volume change of 21% was found to occur in the vicinity of 520 °C–550 °C reversibly. Finally, this study demonstrated that an in situ SXRD experiment supported by DSC measurement is a powerful tool for revealing the reaction routes and identifying new phases occurring in sample-loaded metal tubes.

Preparation of Ni/ZSM-5 and Mo/ZSM-5 catalysts for hydrotreating palm oil into biojet fuel

With the increasing demand for fuel for global usage and CO2 emissions, greener alternatives are needed, especially in biojet fuel production. Catalyst preparation involves the impregnation of Ni and Mo metals into H-ZSM-5 using a dry impregnation method with spray deposition, resulting in Ni/ZSM-5 and Mo/ZSM-5 catalysts. Catalyst characterization utilizes FT-IR, XRD, SAA, SEM-EDX, XRF, and NH3-TPD instruments. The activity and selectivity tests of the catalysts were conducted in the hydrotreating of palm oil using Ni/ZSM-5 monolayer, Ni/ZSM-5 bilayer, Mo/ZSM-5 monolayer, Mo/ZSM-5 bilayer, as well as Ni/ZSM-5 bottom-layer and Mo/ZSM-5 top-layer arrangements. The result showed double-layer Ni/ZSM-5 as the best catalyst in activity and selectivity in producing biojet fuel fractions with consecutive conversion, selectivity, and yield of 29.71%, 84.76%, and 24.34%, respectively. The layers of catalyst affected the catalytic activity and selectivity, resulting in a higher yield.

Enhancing perhydrobenzyltoluene dehydrogenation performance with Co, Mo and Mn metal oxides: A comparative study with Pt/Al2O3 catalyst

In this study, the influence of incorporating Co, Mo and Mn oxides into Pt/Al2O3 catalyst on the dehydrogenation performance of Liquid organic Hydrogen Carrier (LOHCs) is investigated. A notable positive impact on the dehydrogenation process was observed, resulting in enhanced catalytic performance. This effect is associated with improved product desorption and a significant reduction in the by-product formation like methylfluorene. Particularly, the electron-acceptor effect exhibited by molybdenum, emerge as the key factor in enhancing catalytic performance. This effect allowed for the reduction of platinum content without compromising the productivity and selectivity and representing a significant advancement in catalyst design. These findings highlight the potential for Mo-based catalysts to serve as a promising alternatives to Pt-based catalysts in LOHC dehydrogenation processes.

Photocatalytic Removal of the Endocrine Disruptor Chlorpyrifos using a ZnO.MoO3 Composite Supported on Al2O3

AbstractChlorpyrifos is an endocrine disruptor pesticide that induces breast cancer cell proliferation through Estrogen receptor alpha pathway in humans. It also has toxic effects on some beneficial insects like bees, wasps, and arthropods, even low levels of CP can kill fish in water. Thus, it is important to efficiently remove this compound from wastewaters to get rid of its hazardous effects. Al2O3 supported ZnO.MoO3 composite was prepared as an efficient material for photo‐degradation of chlorpyrifos under UV irradiation and characterized by SEM‐EDX, XRD and TG techniques. The XRD analysis showed the orthorhombic structures with band gap of 2.86 eV for ZnO.MoO3/Al2O3 which was 2.96 eV for MoO3/Al2O3. The kinetics of degradation depicted that ZnO.MoO3/Al2O3 afforded a complete degradation of chlorpyrifos with half life of only 3 minutes which otherwise was 24 minutes in the presence of MoO3/Al2O3. The complete mineralization of chlorpyrifos was confirmed by GC/MS analysis, where no peaks of intermediates were recorded. The prepared material also exhibited good recyclability without any leaching of Zn and Mo metals. Thus, ZnO.MoO3/Al2O3 is an efficient and cost effective material for removal of chlorpyrifos. Its potential may also be explored for the removal of other hazardous organic pollutants.

Bi2Se3/ZnSe heterojunction on flexible Mo metal foil for photo electrolysis water splitting application

Abstract The green hydrogen generation by photoelectrochemical (PEC) process emerged as a viable approach to replace non-renewable energy sources, which is done by using semiconducting materials. Recently ZnSe-based heterostructure/junction promise a suitable approach to enhance the PEC performance of photoelectrode. Here we have grown Bi2Se3/ZnSe heterojunction on flexible Mo metal foil by using magnetron sputtering technique toward PEC water splitting application. The crystallinity, structural, and surface morphology of the deposited films were investigated by X-ray diffraction, Raman spectroscopy, and field emission scanning electron microscopy, respectively. The PEC measurements were performed under 100 mW/cm2 (AM = 1.5 G) simulated solar radiation in 0.5 M Na2SO4 aqueous electrolyte solution. The PEC measurements show that Bi2Se3/ZnSe photoelectrode performs better as a photocatalyst, with a photocurrent density of ∼96.4 μA/cm2 (at 0.4 V vs Ag/AgCl), which was found to be three times higher than pristine ZnSe film (∼32.4 μA/cm2). This work suggests the importance of heterojunction towards efficient photoelectrodes for green hydrogen generation.

Synthesis and Mechanism Study of Carbon Nanowires, Carbon Nanotubes, and Carbon Pompons on Single-Crystal Diamonds

Carbon nanomaterials are in high demand owing to their exceptional physical and chemical properties. This study employed a mixture of CH4, H2, and N2 to create carbon nanostructures on a single-crystal diamond using microwave plasma chemical vapor deposition (MPCVD) under high-power conditions. By controlling the substrate surface and nitrogen flow rate, carbon nanowires, carbon nanotubes, and carbon pompons could be selectively deposited. The results obtained from OES, SEM, TEM, and Raman spectroscopy revealed that the nitrogen flow rate and substrate surface conditions were crucial for the growth of carbon nanostructures. The changes in the plasma shape enhanced the etching effect, promoting the growth of carbon pompons. The CN and C2 groups play vital catalytic roles in the formation of carbon nanotubes and nanowires, guiding the precipitation and composite growth of carbon atoms at the interface between the Mo metal catalysts and diamond. This study demonstrated that heterostructures of diamond–carbon nanomaterials could be produced under high-power conditions, offering a new approach to integrating diamond and carbon nanomaterials.

Insights into Dopant-Mediated Tuning of Silica-Supported Mo Metal Centers for Enhanced Olefin Metathesis

Insights into Dopant-Mediated Tuning of Silica-Supported Mo Metal Centers for Enhanced Olefin Metathesis

Performance of sulfided NiMo catalyst supported on pillared bentonite Al and Ti under hydrodeoxygenation reaction of guaiacol

Bio-crude oil is known to be sustainable, eco-environmentally, and an alternative energy source produced by biomass pyrolysis. However, its quality remains relatively low due to a higher oxygen concentration compared to liquid fuels from fossils. Therefore, an upgrading process is necessary through the catalytic hydrodeoxygenation (HDO) process. This work synthesized pillared bentonite using Al and Ti metals as the pillaring agent to produce Al-PILC and Ti-PILC as catalyst support for sulfided NiMo. Their catalytic activity in HDO reaction using guaiacol as a model compound of bio-crude oil were also evaluated. Characterization of the bentonite-pillared materials, including Al-PILC, Mo/Al-PILC, NiMo/Al-PILC, Ti-PILC, Mo/Ti-PILC, and NiMo/Ti-PILC, was performed using Surface Area Analyzer, X-ray Diffractometer (XRD), Temperature-Programmed Desorption of ammonia (NH3-TPD), X-Ray Fluorescence (XRF), and Scanning Electron Microscope (SEM) techniques. The characterization results confirm the pillarization process of bentonite using Al and Ti metals as the pillaring agent, and the preparation of the NiMo catalyst using the stepwise impregnation method was successfully prepared. The NiMo/Ti-PILC catalyst performs a superior conversion value on the HDO guaiacol reaction than other catalysts. A well dispersion of Mo and Ni metals on the surface support (NiMo/Ti-PILC), thus creating numerous active sites of the catalyst after the sulfidation. Variations in time and temperature during the HDO guaiacol reaction significantly affected the conversion.

Coke formation on different metal-modified (Co, Mo and Zr) ZSM-5 in the catalytic pyrolysis of cellulose to light aromatics

Catalytic pyrolysis of biomass is regarded as a promising method for preparing value-added products. However, the main factors limiting the development of the process at present are the low yield of value-added products and poor selectivity, especially for rapid catalyst deactivation due to coke deposition. The present study focuses on the catalytic pyrolysis of cellulose over metal Co-, Mo-, and Zr-loaded catalysts using a falling fixed bed at 600 °C to evaluate the type of coking of the catalysts as well as the effect of the different metal active sites on the formation of coke deposits. The introduction of Co and Mo metal sites increased the light aromatics yield of ZSM-5 from 128.9 mg/g to 147.2 mg/g and 143.0 mg/g. And the yield of coke deposits decreased from 8.3 to 6.8 and 5.1 wt%. The stability evaluation of the catalyst showed that the deactivation degree of ZSM-5 of the supported metal Co was lower than that of commercial ZSM-5, while the ZSM-5 of the supported metal Mo was rapidly deactivated. The deactivation of the catalysts depended more on the morphology or location of the accumulated coke than on the total amount deposited. The clogging of metal and acidic sites on the surface of the zeolite and the pore channels by the amorphous encapsulating coke was the main cause of catalyst deactivation. The metal Mo active sites promoted dehydrogenation coupling and hydrogen transfer during coke formation, forming a more highly disordered multiring structure, and the metal Co active sites were more capable of decomposing macromolecular compounds, olefins and alkanes, and promoted the formation of graphite-like structural carbon.

Role of cooperative effect by Mo and Pd mixed micellar assemblies for displaying the Pt/C like hydrogen evolution reaction

Cooperative effect as well as interfacial engineering are crucial factors for the development of electrochemical hydrogen evolution reaction (HER). Keeping this aspect in mind, a novel mixed micellar film using dodecylamine molybdenum (III) trichloride (MoDDA(I)) and dodecylamine palladium (II) dichloride (PdDDA(I)) was fabricated for electrochemical HER. The mixed micellar film was characterized by various instrumentation techniques to explore its structure and composition i.e. FESEM, AFM, FTIR. In addition, XPS was inserted to understand the underlying mechanism before and after electrolysis. The fabricated surface of mixed micelles was found to be hydrophobic. The efficiency of mix-metallomicelles as an electrocatalyst was checked in acidic media for electrochemical HER. The prepared reverse micellar film was activated by polarization cycles due to the in-situ reduction of metallic components. These metallic cores act as active centers for electrocatalytic HER. The HER activity of Mo-PdDDA(I) was found to be superior as compared with Pt/C. The prepared mixed micelles displayed 29.2 mV dec−1 Tafel slope. First, Mo and Pd based mixed micelles were prepared using a one-pot method. Benefiting from the role of organic media, MoDDA(I) and PdDDA(I) were able to orient in the form of reverse micelles. Wherein, Mo and Pd metal ions are present in the core of the micelles. The excellent activity exhibited by the formation of mix-metallomicelles, a synergic effect between metal ions, and interfacial engineering introduced by the surfactant moiety, which in turn facilitates the adsorption and activation of hydrogen ions on the electrode surface. Additionally, the mixed micelles provide a high surface area for the electrochemical reaction and enhance the conductivity of the electrode.

Unlocking Syngas Synthesis from the Catalytic Gasification of Lignocellulose Pinewood: Catalytic and Pressure Insights.

Modern technologies transform biomass into commodity chemicals, biofuels, and solid charcoal, making it appear as a renewable resource rather than organic waste. The effectiveness of Mo, Fe, Co, and Ni metal catalysts was investigated during the gasification of lignocellulosic pinewood. The primary goal was to compare the performance of iron and nickel catalysts in the low- and high-pressure production of syngas from pinewood. This is the first study that has reported high-pressure gasification of pinewood without the use of an external gasifying agent, producing syngas containing hydrogen, carbon monoxide, and carbon dioxide along with considerable amounts of methane with or without a catalyst. Also, the same gasification at low pressures was compared. In this study, the iron catalyst produces syngas more efficiently at higher pressure and 800 °C, and contains 43 mol % H2, 22 mol % CO2, 26 mol % CH4, and 8 mol % CO in comparison to the nickel catalyst. High pressure produces a large amount of methane too. The nickel catalyst produces higher syngas at low pressure and 850 °C, and contains 55 mol % H2, 9 mol % CO2, 5 mol % CH4, and 30 mol % CO. Low-pressure gasification produces less amounts of CH4 and CO2. Also, the H2/CO ratio is ∼1.81 using the nickel catalyst at low pressures, which is good for utilizing syngas as a feedstock. These results highlight the importance of catalyst selection, reactor configuration, and operating circumstances in adjusting gasification product composition. The study's findings provide information about optimizing syngas production from pinewood, which is critical for the development of sustainable and efficient energy conversion technologies.

Hydrocracking Rubber Seeds Oil for Biofuel Production Using Bifunctional Sarulla‐Derived Natural Zeolite–Ni and Ni–Mo/SNZ Catalyst

Rubber seeds, due to their rich vegetable oil content, emerge as a promising substrate for biofuel production. Harnessing the progressive catalytic hydrocracking methodology, this research delves into the activation of Sarulla‐derived natural zeolite followed by Ni and Ni–Mo metal impregnation, subsequently subjecting rubber seed oil to hydrocracking at 400, 450, and 500 °C under atmospheric pressure at 0.1 MPa. Zeolite characteristics undergo notable transformations postmetal impregnation. Importantly, at 500 °C, gasoline fraction selectivity exhibits superior efficacy, with the Ni/SNZ‐A catalyst demonstrating consistently high selectivity (>85%) across varied temperatures. Posthydrocracking reveals an amplification in n‐paraffin, aromatic, olefin, and methyl ester profiles to 19.6%, 7.3%, 25.7%, and 17.7%, respectively, contrasting the diminution of cycloparaffin, carboxylic acid, and ketones to 3.6%, 0.2%, and 2.5%, respectively. The aforementioned discoveries hold significant importance in the realm of further investigation into the generation of gasoline fractions through the utilization of natural zeolite catalysts and the incorporation of metals with lower mass, all conducted under atmospheric pressure conditions with the ultimate objective of mitigating production expenses.

Source-oriented risk assessment of heavy metal(loid)s in agricultural soils around a multimetal smelting area near the Yellow River, China.

Heavy metal(loid) (HM) contamination in agricultural soils, particularly in areas severely impacted by smelting industries, has attracted worldwide attention. In this study, agricultural soils were collected in a flourishing multimetal smelting area near the Yellow River in central China. By an integrated approach encompassing the positive matrix factorization model, ordinary kriging interpolation and hierarchical clustering analysis (PMF-OK-HC), a total of four major sources and their mass contributions were identified, namely, soil parent material (56.6%), industrial waste and Mo smelting (24.0%), metal smelting and traffic emissions (12.8%), and coal combustion (6.7%). On this basis, the health risk of HMs was evaluated by Monte Carlo simulations and showed that a higher risk, with a higher proportion of exceeding-thresholds risk, was observed for children than for adults in terms of both noncarcinogenic and carcinogenic risks. Exposure pathways of oral ingestion in children could result in a higher attributed risk than other pathways. Furthermore, source-oriented risk assessment (SORA) revealed that the sources of coal combustion, industrial waste and Mo smelting had the highest contributions to noncarcinogenic and carcinogenic risks. Overall, for effective environmental management in agricultural soil, the framework of SORA was verified as an effective tool in the identification of the priority control of HMs and their sources.

Characteristics of Ore-Forming Fluids and Genesis of the First Mining Area and Eastern Ore Section of the Pulang Porphyry Copper Deposit, Southeastern China: A Comparative Study

The Pulang copper deposit, formed in the Late Triassic, is the largest porphyry Cu-Mo-Au deposit in the eastern Tethys, and its genetic type and mineralization potential have received widespread attention. Identifying the characteristics of ore-forming fluids and the sources of ore-forming materials in the deep and peripheral ore bodies of Pulang is particularly important for constructing a complete porphyry copper mineralization system. Based on detailed core logging and geological observations, this article provides extensive petrographic, fluid inclusion micro-thermometry, laser Raman spectroscopy, and H-O-S isotope data on the veins of the main mineralization stage (B veins) in the first mining area and eastern ore section of the Pulang porphyry copper deposit. The genetic correlation between the eastern ore section and the first mining area is clarified, and their mineralization potential is inferred. The results indicate that the deep vein bodies in the first mining area exhibit multi-stage characteristics, and the fluid in B veins exhibits both high-temperature and salinity characteristics. The magma-derived early ore-forming fluids underwent processes such as boiling and experienced immiscibility during meteoric water mixing, which could be the primary mechanism of the precipitation of Cu, Mo, Au, and other metals. The outer eastern ore section is located in a medium-to-low-temperature hydrothermal mineralization zone far from the mineralization center. This outer eastern ore section is a distant part of the magmatic–hydrothermal system of the first mining area.

Eliminating surface cracks in metal film-polymer substrate for reliable flexible piezoelectric devices

In a flexible piezoelectric-metal-polymer device, the occurrence of surface cracks in metal-polymer interface may cause unstable metal connections, unreliable piezoelectric yield, poor passivation behaviour and metal electrode delamination. In this study, the properties of polydimethylsiloxane (PDMS) polymer substrate are optimised, and the sputter-deposition of aluminium (Al) and molybdenum (Mo) metal film layer is controlled to eradicate cracks and promote only surface wrinkles on large area metal-polymer interface. The PDMS substrate thickness of ∼123.8 µm, 20:1 prepolymer base to curing agent weight ratio, 50 °C PDMS curing temperature and 30 min of Al sputtering time have been discovered to produce crack-free wrinkle-only Al thin film layer on PDMS substrate. The Al thin film is 100 % conductive over large area and adhere well on PDMS with 0 % of Al removal. The grown zinc oxide (ZnO) and aluminium nitride (AlN) piezoelectric layer on the improved Al-PDMS are of good crystal quality, generating low leakage current and decent piezoelectric voltage. The attained crack-free wrinkled-only metal film-polymer substrate interface is vital for flexible piezoelectric-metal-polymer device to perform well as an acoustic sensor, energy harvester, or even as an insulation/buffer layer in stretchable electronics.