Decomposition Of Water Research Articles

Synergistic dual built-in electric fields in 1T-MoS2/Ni3S2/LDH for efficient electrocatalytic overall water splitting reactions

Designing cost-effective electrocatalysts for water decomposition is crucial for achieving environmental-friendly hydrogen production. A transition metal sulfide/hydroxide electrocatalyst (1T-MoS2/Ni3S2/LDH) with double heterogeneous interfaces was developed through a two-step hydrothermal assisted electrodeposition method. The presence of the two built-in electric fields not only accelerated the charge transfer at the interface, but also enhanced the adsorption of the reactants and intermediate groups, and therefore improved the reaction rate and overall catalytic performance. The results suggest that the 1T-MoS2/Ni3S2/LDH catalysts display exceptional electrocatalytic reactivity. Under alkaline conditions, the overpotential of the electrocatalyst was 187 (η50) mV for OER and 104 (η10) mV for HER. Furthermore, the two-electrode system assembled by the electrocatalyst needs only a voltage of 1.55 V to deliver a current density of 10 mA cm−2. Our result provides a simple and effective methodical approach to the design of dual heterogeneous interfacial electrocatalysts.

Hydrogen production and stainless steel corrosion during water decomposition under gamma radiation

The hydrogen production during radiation-thermal processes of water and stainless steel systems at different temperatures was studied. As a result of the energy transfer of ionizing radiation and the interaction of active intermediates with the initial components, the formation of molecular hydrogen occurred. With an augment in temperature from 300 to 673 K, an increase in hydrogen yield was reported. It has been established that at a temperature of 673 K, a chain mode of transformation of the primary products of stainless steel radiolysis into molecular hydrogen was obtained. The values of G(H2) were 2.50, 3.95, 5.0, 7.11 and 10.5 at 300, 373, 473, 573 and 673 K temperature. On the other hand, these values were 5.11, 9.15, 11.0, 12.5, 16.5 and 25.5 molecules/100eV at 80, 160, 240, 320, 400 and 480 Gy, respectively. At 473 K, an oxidative layer was formed on the surface of stainless steel, while at 523 K, insoluble surface oxidizing products were formed. The main radiation corrosion was observed at T ≥ 573K. At 300–673K temperature ranges, the corrosion rate of stainless steel increased by 4–5 times during radiation-heterogeneous procedures. As a result of these processes, an oxide film was formed on the surface, which prevented further oxidation of the metal. This work is important for hydrogen production and stainless steel corrosion. This paper will be highly useful for hydrogen production and the use of stainless steel in nuclear reactors.

The Temperature of Pretreatment on Microstructure Change of Lump Ore and Improvement of Metallurgical Properties

Goethite is one of the most common minerals in iron ore, and is the main source of internal crystal water generated during the heating process of lump ore. To address this challenge, three measures are proposed: first, minimizing the decomposition of crystalline water upon the introduction of lump ores into the furnace; second, reducing the heat absorption of water vapor within the furnace; and third, increasing the proportion of lump ores being introduced into the furnace. With this in mind, the lump ore preheating treatment technology is introduced. By preheating the lumps at different temperatures, the influence of pretreatment on the reduction and soft melting of the lumps is studied. The results show that at different preheating temperatures, due to the transformation of FeOOH to Fe2O3, the natural goethite gradually changes from natural granular to spherical at higher preheating temperatures. When the preheating temperature is 400–700 °C, the coexisting phase of goethite and hematite in the pores changes obviously. The metallurgical properties of lump ore change dramatically. When the temperature is lower than 400 °C or higher than 700 °C, almost all goethite in lump ore is transformed into hematite, and the morphology does not change.

Enhanced visible light-driven hydrogen evolution in non-precious metal Ni2P/CdIn2S4 S-type heterojunction via rapid interfacial charge transfer

Strong light absorption capacity and effective separation of photogenerated charge are the keys to photocatalytic water decomposition, which is usually solved by constructing heterojunction methods. In this work, a novel n-n interwoven Ni2P/CdIn2S4 S-type heterojunction photocatalyst was prepared by hydrothermal method for efficient photocatalytic hydrogen evolution. After a series of characterization and performance tests, under simulated sunlight irradiation at 6 °C (λ > 420 nm), the hydrogen production of Ni2P/CdIn2S4 composite with the best performance can reach 6 mmol/g/h, which is not only 48 times that of pure CdIn2S4, but also 17.2 times that of the expensive metal Pt (CIS–1Pt). By changing the temperature, the hydrogen production of Ni2P/CdIn2S4 reached 8.7 mmol/g/h at 27.5 °C, while its AQY reached 7.7 % and 6.6 % at 420 nm and 475 nm, respectively. In addition, the possible photocatalytic mechanism was analyzed by band structure and XPS diagram, and it was confirmed that the internal electric field of the S-type heterojunction accelerated the photogenerated charge transition and enhanced the hydrogen evolution ability. This effectively compensated for the limitations of severe carrier recombination and low active sites in CdIn2S4 photocatalysts. Therefore, this work provides some help for the construction of non-precious metal S-type heterojunctions for photocatalytic hydrogen production.

Rechargeable zinc-water battery for sustainable hydrogen generation

Metal-water primary batteries hold promise for distributed hydrogen production but suffer from limited renewability of metal electrodes in aqueous electrolytes. Here, we introduce a novel concept of a rechargeable zinc-water battery featuring a reversible zinc anode paired with a bifunctional water electrolysis electrode, realized in a specially designed aqueous electrolyte-a mild zinc triflate aqueous electrolyte with the addition of ethylenediaminetetraacetic acid disodium (EDTANa2). The system enables high-purity hydrogen production during discharge and high-purity oxygen production during charge in a membrane-free setup. In the zinc-water battery, EDTANa2 enhances the water-splitting electrode's performance by replacing hydrophobic OTF- anions, ensuring optimal water activity. Additionally, EDTANa2 enhances Zn electrode reversibility by chelating Zn2+, preventing solvated water decomposition during zinc deposition. This integrated battery continuously undergoes charge-discharge cycles for over 55 h at a current density of 6 mA cm-2. Moreover, it achieves a high hydrogen evolution rate of 12.5 mL cm-2 h-1, enabling cost-effective, high-purity hydrogen production without expensive membranes. These findings open new avenues for sustainable hydrogen generation and energy storage in nano energy systems.

High transmittance BiVO4 thin-film photoanodes by reactive magnetron sputtering for a photovoltaic-photoelectrocatalysis water splitting system

As the system with the highest solar hydrogen conversion efficiency, the further improvement of photovoltaic-photoelectrocatalysis (PV-PEC) efficiency is dependent on the light transmittance, activity and stability of the photoanode. Here, a highly permeable BiVO4 thin film was fabricated through controlled magnetron sputtering. The thickness of the thin film was merely 345 nm, while its transmittance in the visible light range reached as high as 70%. Moreover, large-scale production of such films could be achieved. By incorporating NiFeOx oxygen extraction cocatalyst, under AM 1.5G illumination, the photocurrent density at 1.23 V on reversible hydrogen electrode (RHE) increased to 4.2 mA cm−2 and the incident photon-current conversion efficiency reached 70%. A PV-PEC system was designed to efficiently harness sunlight by integrating the photoanode with a solar photovoltaic panel. Upon connection with the solar photovoltaic panel (with an efficiency of only 7%), spontaneous water decomposition could be achieved, resulting in a solar-to-hydrogen conversion efficiency (ηSTH) of 4.2% for the series system. This study contributes to the realization of cost-effective and highly efficient PV-PEC hydrogen production.

C3N5 nanosheets decorated with Cu–Pt alloy nanoparticles toward efficient photocatalytic hydrogen evolution

The construction of highly efficient photocatalysts for generating high-purity hydrogen (H2) through a sustainable water decomposition system is a feasible option to replace conventional non-renewable energy resources. Here, we report a simple chemical reduction approach to embed Cu–Pt alloy nanocrystals on the C3N5 (CN) matrix, creating a Schottky heterojunction. The structural morphology, crystal phase, light-harvesting capacity, and photo-electrochemical properties of as-prepared heterostructures were investigated. The uniformly anchored Cu–Pt alloy nanocrystals improve the photocatalytic H2 evolution (PHE) activity by promoting the separation and transfer of photogenerated carriers and inhibiting recombination. Meanwhile, the alloyed nanocrystals strengthen the absorption of incident light energy, inducing photothermal energy. This improves the charge carrier separation and promotes the surface reaction kinetics. The PHE performance of as-developed catalysts could be adjusted by optimizing the molar ratio of Cu/Pt ions. Among them, the optimal Cu1Pt3/CN photocatalyst yields a higher PHE performance (672.85 μmol g−1 h−1). Notably, the Cu1Pt3/CN catalyst also reveals an enhanced photocatalytic activity for H2 evolution in natural seawater. The possible PHE mechanism in CuPt/CN heterostructures is discussed toward the role of CuPt alloy deposition in boosting photocatalytic efficiency.

Two-Dimensional Sc2CCl2/XSe2(X=Mo, Pt) van der Waals Heterojunctions: Promising Photocatalytic Hydrogen Evolution Materials.

In the field of photocatalysis, new heterojunction materials are increasingly explored to achieve efficient energy conversion and environmental catalysis under visible light and sunlight. This paper presents a study on two newly constructed two-dimensional van der Waals heterojunctions, Sc2CCl2/MoSe2 and Sc2CCl2/PtSe2, using density-functional theory. The study includes a systematic investigation of their geometrical structure, electronic properties, and optical properties. The results indicate that both heterojunctions are thermodynamically, kinetically, and mechanically stable. Additionally, Bader charge analysis reveals that both heterojunctions exhibit typical type II band properties. However, the band gap of the Sc2CCl2/MoSe2 heterojunction is only 1.18 eV, which is insufficient to completely cross the reduction and oxidation (REDOX) potential of 1.23 eV, whereas the band gap of Sc2CCl2/PtSe2 heterojunction is 1.49 eV, which is theoretically capable for water decomposition. The subsequent calculation of the Sc2CCl2/PtSe2 heterojunction demonstrate excellent hole carrier mobility and high efficiency light absorption in the visible light range, facilitating the separation of photogenerated electrons and holes. More importantly, Sc2CCl2/PtSe2 vdW type II heterojunction can achieve full water decomposition from pH 1 to pH 4, and its thermodynamic feasibility is confirmed by Gibbs free energy results. The aim of this study is to develop materials and analyses that will result in optoelectronic devices that are more efficient, stable, and sustainable.

Bimetallic electrocatalysts based on polyoxometalate for hydrogen evolution and urea oxidation reaction

Electrochemical water decomposition is an efficient and environmentally friendly method for producing hydrogen. Because of the high voltage required for water electrolysis, using anodic urea oxidation process (UOR) to replace the oxygen evolution reaction can significantly cut energy usage. In this paper, hydrogen evolution reaction (HER) and urea oxidation process (UOR) electrocatalysts were synthesized by one-step carbonization using giant polyoxomolybdate cluster Mo132 and triethylamine at different temperatures. Ni/MoN@NC obtained at 800 °C shows good HER effect in the acidic electrolyte, an overpotential of 94 mV can provide the current density of 10 mA cm−2. Ni/NiO@NC obtained by calcination at 400 °C exhibits good UOR performance, in which the potential is 1.41 V when the current density is 10 mA cm−2. Efficient HER performance depends on the synergy of Ni and MoN. The highly efficient UOR is derived from the hierarchical structure of Ni and NiO. Furthermore, the porous structure also enhances the full contact between electrolyte and active sites, the catalytic performance of the catalyst was improved benefit to improve the catalytic activity. This work affords a general approach to simply synthesize efficient hydrogen producing materials for HER and small molecules oxidation fields.

GeC/SnSe2 van der waals heterostructure: A promising direct Z-scheme photocatalyst for overall water splitting with strong optical absorption, high solar-to-hydrogen energy conversion efficiency and superior catalytic activity

To alleviate the energy crisis and achieve green energy conversion, the heterojunctions that can be applied to the photocatalytic decomposition of water have attracted attention. In this paper, we design a novel two-dimensional GeC/SnSe2 heterostructure and investigate in detail the structural stability, electronic characteristics, photocatalytic activity and optical behavior as well as the effects due to the applied strain based on the first-principles. Firstly, the most stable γ-stacking mode is determined by combining energy comparison, thermodynamic and dynamic studies. Second, the analysis of electronic properties demonstrates that the GeC/SnSe2 heterostructure exhibits a type-II energy band arrangement and a direct Z-scheme photocatalytic mechanism. This pivotal aspect enhances the separation of photogenerated carriers at the interface and facilitates the active participation of the most proficient materials in oxidation-reduction processes during photocatalytic hydrolysis reactions. The hydrolysis reaction's Gibbs free energy shift demonstrates the GeC/SnSe2 heterostructure's superior photocatalytic activity in neutral and alkaline environments and can spontaneously carry out the overall hydrolysis reaction, and this outstanding ability is not affected by the −4% to 4% strain range. In addition, the GeC/SnSe2 heterostructure has outstanding solar-to-hydrogen efficiency (58.18%) and excellent light absorption capability (up to 4×105cm−1) within visible light. The implications of these discoveries point towards the direct Z-scheme GeC/SnSe2 heterostructure holds promise as an excellent candidate for photocatalytic water splitting applications.

Efficient visible light photocatalytic green hydrogen production from Dy2O3 combined with nitrogen-deficient g-C3N4

The efficient construction of heterojunction photocatalysts has a crucial significance in achieving the decomposition of water for hydrogen generation. This work successfully prepared nitrogen-deficient g-C3N4 (ND-g-C3N4) and combined it with dysprosium oxide (Dy2O3) through high-temperature calcination to create a type II heterojunction photocatalyst (Dy2O3/ND-g-C3N4). Notably, under visible light, the Dy2O3/ND-g-C3N4 photocatalyst demonstrated impressive hydrogen production rates in both ethylene glycol and glucose solutions. Specifically, the photocatalyst achieved H2 generation rates of 463.256 and 510.305 μmol⋅g−1⋅h−1 in ethylene glycol and glucose solutions, respectively. And the quantum yield could be up to 21.76% and 23.96%, respectively. Furthermore, the photocatalytic reforming of glucose for H2 production yielded valuable intermediate products. The f-shell layer in the Dy2O3 had a significant function in enhancing photocatalytic hydrogen production efficiency. This improvement was attributed to the ability of the f-shell layer to capture excited electrons, thereby decreasing the rate of recombination of exciton pairs.

Spontaneous enhanced photocatalytic overall water splitting on AlO/WSi2N4 vdW heterojunction

Completely achieving spontaneous water splitting without sacrificing co-catalysts poses a significant challenge, as factors such as electrical, optical, and catalytic activity can limit the conversion efficiency of solar energy to hydrogen. Herein, we propose a type-II van der Waals heterostructure composed of vertically stacked AlO and WSi2N4, and systematically investigate its mechanism and potential for catalyzing water splitting. Photon-induced photocatalytic water splitting takes advantage of the staggered energy bands of the heterojunction, effectively promoting the separation of photogenerated carriers and thus enhancing catalytic efficiency. In neutral water environment, the band edge position of AlO/WSi2N4 aligns with the redox potential required for water decomposition. Thermodynamic analysis of the oxygen and hydrogen evolution reactions indicates that the external potential provided by photogenerated carriers is expected to trigger spontaneous water decomposition. Moreover, with its high electron mobility (4800.62 cm2/Vs) and a solar-to-hydrogen energy conversion efficiency of up to 19.98 %, the AlO/WSi2N4 heterojunction demonstrates substantial potential as a photoelectric catalyst. This research introduces a promising avenue for efficient photocatalytic production of clean energy.

The research progress on photocatalytic performance of graphene-based nanocomposites

As soon as nanomaterials were discovered, they attracted a lot of attention because of their unique and excellent properties and became major hot research. They are regarded as the most promising materials in the 21st century. With the growth of industrial production, photocatalytic technology has been pursued as an efficient, green, and economical way of industrial production and treatment of pollution. However, the low light energy utilization of traditional semiconductor materials is a drawback that cannot be ignored. Graphene, as one of the most common and widely used 2D nanomaterials, has a special structure and characteristics that can effectively solve this problem. The paper briefly introduces the structure, properties, preparation method, and basic principle of photocatalysis of graphene. At the same time, a review is provided on the application of graphene-based composite materials in the field of photocatalysis, including dye degradation, photocatalytic treatment of other emerging pollutants, photocatalytic treatment of air pollutants, and water decomposition. By summarizing and integrating the photocatalytic properties of several graphene-based composites, this article lays the foundation and helps to discover new graphene composites.

Ru-Doped NiFe-MIL-53 with Facilitated Reconstruction and Active Hydrogen Supplement for Enhanced Nitrate Reduction.

The Electrochemical reduction of nitrate to ammonia (NH3) is a process of great significance to energy utilization and environmental protection. However, it suffers from sluggish multielectron/proton-involved steps involving coupling reactions between different reaction intermediates and active hydrogen species (Hads) produced by water decomposition. In this study, a Ru-doped NiFe-MIL-53 (NiFeRu-MIL-53) supported on Ni foam (NF) has been designed for the nitrate reduction reaction (NO3RR). The NiFeRu-MIL-53 exhibits excellent NO3RR activity with a maximum Faradaic efficiency (FE) of 100% at -0.4 V vs. RHE for NH3 and a maximum NH3 yield of 62.39 mg h-1 cm-2 at -0.7 V vs. RHE in alkaline media. This excellent performance for the NO3RR is attributed to a strong synergistic effect between Ru and reconstructed NiFe(OH)2. Additionally, the doped Ru facilitates water dissociation, leading to an appropriate supply of Hads required for N species hydrogenation during NO3RR, thereby further enhancing its performance. Furthermore, in situ Raman analysis reveals that incorporating Ru facilitates the reconstruction of MOFs and promotes the formation of hydroxide active species during the NO3RR process. This work provides a valuable strategy for designing electrocatalysts to improve the efficiency of the reduction of electrochemical nitrate to ammonia.

Enhanced hydrogen production through cracking of ammonia water using liquid plasma on titanate-based perovskite catalysts

In this study, a mass production of hydrogen was studied through cracking of ammonia water using liquid plasma. A new FexNi1-xTiO3 perovskite composite with significantly improved visible-light sensitivity was synthesized to further improve the photochemical reaction activity. It is applied to hydrogen production from the decomposition of ammonia water using liquid plasma. In this reaction, a large amount of hydrogen is produced with a small amount of nitrogen gas; moreover, oxygen is produced by liquid plasma discharge and no CO2 byproduct is produced. Titanate-based perovskite catalysts have also been used in decomposition reactions. Titanate-based perovskite catalysts exhibiting high rates of hydrogen production during decomposition were obtained for the plasma and photocatalytic decomposition of aqueous ammonia. FexNi1-xTiO3, which is a newly synthesized ABTiO3-type titanate, showed a higher rate of hydrogen production (approximately 140 L/(g·h)) than other titanate-based perovskites. Furthermore, the FexNi1-xTiO3 exhibited the highest sensitivity to UV and visible light. Its high photosensitivity helped improve the photocatalytic activity in the decomposition of ammonia in water using plasma.

Unique ping-pong daisy-like catalysts: Efficient overall hydrolysis catalysis driven by vanadium-doped Fe2P and Co3(PO4)2 nanosheet composites

Balancing catalytic activity and durability remains a challenge in the development of high performance, inexpensive and durable electrocatalysts. In this study, fully hydrolyzed composite catalyst V–Fe2P@Co3(PO4)2/NF with ping-pong daisy-like morphology was synthesized using conventional hydrothermal and chemical vapor deposition (CVD) processes. In alkaline electrolyte, V–Fe2P@Co3(PO4)2/NF showed excellent electrochemical performance, achieving a current density of 10 mA cm−2 when the driving overpotentials for the hydrogen production reaction (HER) and oxidation reaction (OER) were 56 mV and 178 mV, respectively. Meanwhile, V–Fe2P@Co3(PO4)2/NF demonstrated good durability in terms of both HER and OER stability. Furthermore, the driving voltage required for the electrolyser assembled with V–Fe2P@Co3(PO4)2/NF as the electrode is lower than that of the RuO2/NF||Pt/C/NF electrode, both of which have driving voltages of 1.503 and 1.562 V (10 mA cm−2), respectively. Meanwhile, it achieves a Faraday efficiency of 95%. This study offers a feasible solution towards synthesizing and applying bifunctional water decomposition electrocatalysts.

Achieving deep intratumoral penetration and multimodal combined therapy for tumor through algal photosynthesis

BackgroundElevated interstitial fluid pressure within tumors, resulting from impaired lymphatic drainage, constitutes a critical barrier to effective drug penetration and therapeutic outcomes.ResultsIn this study, based on the photosynthetic characteristics of algae, an active drug carrier (CP@ICG) derived from Chlorella pyrenoidosa (CP) was designed and constructed. Leveraging the hypoxia tropism and phototropism exhibited by CP, we achieved targeted transport of the carrier to tumor sites. Additionally, dual near-infrared (NIR) irradiation at the tumor site facilitated photosynthesis in CP, enabling the breakdown of excessive intratumoral interstitial fluid by generating oxygen from water decomposition. This process effectively reduced the interstitial pressure, thereby promoting enhanced perfusion of blood into the tumor, significantly improving deep-seated penetration of chemotherapeutic agents, and alleviating tumor hypoxia.ConclusionsCP@ICG demonstrated a combined effect of photothermal/photodynamic/starvation therapy, exhibiting excellent in vitro/in vivo anti-tumor efficacy and favorable biocompatibility. This work provides a scientific foundation for the application of microbial-enhanced intratumoral drug delivery and tumor therapy.Graphical

Preparation of nanoporous TiOx powder and its enhanced photocatalytic N2 to NH3 conversion by solar-driven interfacial water evaporation

At present, the limited efficiency in ammonia generation poses significant challenge to the widespread practical implementation of photocatalytic nitrogen reduction to ammonia (PNRN). In this study, we synthesized a nanoporous TiOx powder (Alloy-RTO) by rapid breakdown anodization of TA13 alloy and subsequent magnesiothermic reduction. The Alloy-RTO exhibited superior photothermal and photocatalytic properties owing to its multicomponent and interconnective nanoporous structure, and the electronic band structure is suitable for efficient PNRN. Notably, through synergistic integration of PNRN with solar-driven interfacial water evaporation technology (SDIWE), the ammonia production rate was further enhanced, and a multifaceted role of SDIWE in enhancing PNRN was proposed: (1) increasing temperature of Alloy-RTO to promote PNRN; (2) raising temperature to accelerate ammonia water decomposition and facilitate PNRN; and (3) generating plenty of gaseous water to accelerate PNRN. This study presents an effective strategy for preparing nanoporous TiOx and highlights the pivotal role of SDIWE in promoting PNRN.

Lability of sedimentary organic nitrogen estimated from amino acids in a reservoir on land reclaimed from Isahaya Bay, Kyushu, Japan

In 1997, the inner part of Isahaya Bay on the west coast of the Ariake Sea was separated from the sea by dikes, leading to the formation of a freshwater reservoir. Since the Isahaya Reclamation Project began in the 1990s, red tides have become more common in the bay. Studies suggested that a non-negligible amount of NH4+ was regenerated from organic matter decomposition in the turbid water drained from the reservoir into the bay, and this drainage water might be an important source of NH4+ for red tides in the bay. Although labile organic matter in the turbid water might also originate from resuspended sediments in the reservoir induced by the drainage process, the potential for the resuspended sedimentary organic matter to serve as an NH4+ source has never been evaluated. In this study, we found that sediments near the drainage gates on the dike in the reservoir contained high levels of amino acids and NH4+. In addition, the NH4+ concentrations were positively correlated with amino acids concentrations. This result can be explained by increasing NH4+ production according to labile organic nitrogen accumulation in the sediments near the dike. The result of our study suggests that the sediment resuspension near the dike induced by drainage might be a source of bioavailable nitrogen for Isahaya Bay.

Photon-counting detector step-wedge calibration enabling water and iodine material decomposition

Photon-counting detector computed tomography (PCD-CT) has demonstrated improvements in conventional image quality compared to energy integrating detector (EID) CT. PCD-CT has the advantage of being able to operate in conventional and spectral mode simultaneously by sorting photons according to selected energy thresholds. However, to reconstruct spectral images PCD-CT requires extensive calibration and specifically fine-tuning a spectral response. This response is then used to perform material decomposition (MD). We propose a step-wedge phantom made of water and iodine to calibrate a prototype PCD-CT system. Four methods were tested and compared based on calibration accuracy and CT image quality. The exhaustive PCD response was not well calibrated, but a reduced model was defined that was able to perform accurate water/iodine MD and to reduce the ring artifact intensity. The impact of the number of energy bins (from two to seven) was also studied. The number of bins did not affect the spectral accuracy. However, compared to the two energy bin configuration, the seven bin configuration decreased the noise by 10% and 15% in the water and iodine maps, respectively. The model was tested on ex-vivo tissue samples injected with iodine to demonstrate the results of the water/iodine MD on biological materials.