Amorphous Phosphate Research Articles

Highly Stable Amorphous (Pyro)phosphate Aggregates: Pyrophosphate as a Carrier for Bioactive Ions and Drugs in Bone Repair Applications

Highly Stable Amorphous (Pyro)phosphate Aggregates: Pyrophosphate as a Carrier for Bioactive Ions and Drugs in Bone Repair Applications

Triphasic Ni2P-Ni12P5-Ru with Amorphous Interface Engineering Promoted by Co Nano-Surface for Efficient Water Splitting.

This research designs a triphasic Ni2P-Ni12P5-Ru heterostructure with amorphous interface engineering strongly coupled by a cobalt nano-surface (Co@NimPn-Ru) to form a hierarchical 3D interconnected architecture. The Co@NimPn-Ru material promotes unique reactivities toward hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in alkaline media. The material delivers an overpotential of 30mV for HER at 10mAcm-2 and 320mV for OER at 50 mAcm-2 in freshwater. The electrolyzer cell derived from Co@NimPn-Ru(+,-) requires a small cell voltage of only 1.43V in alkaline freshwater or 1.44V in natural seawater to produce 10mA cm-2 at a working temperature of 80°C, along with high performance retention after 76h. The solar energy-powered electrolyzer system also shows a prospective solar-to-hydrogen conversion efficiency and sufficient durability, confirming its good potential for economic and sustainable hydrogen production. The results are ascribed to the synergistic effects by an exclusive combination of multi-phasic crystalline Ni2P, Ni12P5, and Ru clusters in presence of amorphous phosphate interface attached onto cobalt nano-surface, thereby producing rich exposed active sites with optimized free energy and multi open channels for rapid charge transfer and ion diffusion to promote the reaction kinetics.

Different survival strategies of the phosphate-mineralizing bacterium Enterobacter sp. PMB-5 in response to cadmium stress: Biomineralization, biosorption, and bioaccumulation

The phosphate-mineralizing bacteria (PMBs) has shown great potential as a sustainable solution to support pollution remediation through its induced mineralization capacity. However, few studies have been conducted on the mechanism of cadmium (Cd) tolerance in PMBs. In this study, a PMB strain, Enterobacter sp. PMB-5, screened from Cd-contaminated rhizosphere soil, has high resistance to Cd (540 - 1220 mg/L) and solubilized phosphate (232.08 mg/L). The removal experiments showed that the strain PMB-5 removed 71.69–98.24% and 34.83–76.36% of Cd with and without biomineralization, respectively. The characterization result of SEM, EDS, TEM, XPS and XRD revealed that PMB-5 induced Cd to form amorphous phosphate precipitation through biomineralization and adopted different survival strategies, including biomineralization, bioaccumulation, and biosorption to resistance Cd in the microbial induced phosphate precipitation (MIPP) system and the non-MIPP system, respectively. Moreover, the results of whole genome sequencing and qRT-PCR indicated that phosphorus metabolism genes such as pst, pit, phn, ugp, ppk, etc. and heavy metal tolerance genes (including ion transport, ion efflux, redox, antioxidant stress), such as czcD, zntA, mgtA, mgtC, katE, SOD2, dsbA, cysM, etc. were molecular for the PMB-5 mineralization and Cd tolerance of PMB-5. Together, our findings suggested Enterobacter sp. PMB-5 is a potential target for developing more effective bioinoculants for Cd contamination remediation.

Reactivity of MSWI-fly ash in Mg-K-phosphate cement

In this study, the behaviour and reactivity of Municipal Solid Waste Incineration Fly Ash (MSWI-FA), introduced in the formulation of magnesium potassium phosphate cement (MKPC), was investigated by considering the waste either as fully inert or reactive. MSWI-FA induced structural and compositional modifications in MKPC as a consequence of dissolution/precipitation processes which involved many MSWI-FA elements (e.g., Ca, Mg, Al, Si, Zn) and led to the formation of mostly amorphous phosphate secondary products. The reaction path has been described in terms of the early fast dissolution of MSWI-FA, with precipitation of very low solubility phases, and subsequent late precipitation due to pH changes and water subtraction during MKPC gelification. The increase in amorphous content peaked to 50 wt.% and it has been related to the improved behaviour with respect to the leaching of heavy metals (reduced by 70-99%), pointing to this cement as an excellent matrix for their chemical stabilization. The obtained MKPC microstructure exhibited better mechanical performance, with an improvement of up to 60% in compressive strength. All in all, the results indicated that the incorporation in MKPC is a viable recycling opportunity for MSWI-FA, although, for an effective cement formulation, its reactivity must be taken into account.

Pure Amorphous and Ultrathin Phosphate Layer with Superior Ionic Conduction for Zinc Anode Protection.

Fast and uniform ion transport within the solid electrolyte interphase (SEI) is considered a crucial factor for ensuring the long-term stability of metal electrodes. In this study, we present the fabrication of ultrathin artificial interphases consisting of a zinc phosphate nanofilm with pure amorphous characteristics and a surfactant overlayer. The thickness of the interphases can be precisely controlled within the range of a few tens of nanometers. We explore the impact of artificial SEI structure, including thickness and crystallinity, on its protective capabilities. The pure amorphous phosphate layer with optimized nanoscale thickness is found to provide an abundance of short and isotropic ion migration pathways and a low diffusion energy barrier. These features facilitate rapid and homogeneous Zn2+ transportation, resulting in compact and planar zinc deposition. Meanwhile, the hydrophobic alkyl moieties of the overlayer prevent disassociation of water at the interface. As a result, this nanofilm endures ultralong cycling stability with a low overpotential and enables high Zn plating/stripping reversibility. The Zn||MnO2 full cell shows a stable cycle life for 700 cycles under practical conditions of lean electrolyte, high areal capacity cathode, and limited Zn excess. These findings provide insights into the design and optimization of SEI layers for protection of metal anodes.

Surface Adsorption of Amorphous Phosphate on RuNi-Doped Molybdate for the Hydrogen Evolution Reaction.

Developing highly active and cost-effective electrocatalysts is critical for enhancing the intrinsic performance of electrocatalytic water splitting. Oxoanion-based compounds, such as phosphates and molybdates, have emerged as promising electrocatalysts owing to their advantageous properties of nontoxicity, low price, and strong water adsorption ability. However, their relatively inferior activity has impeded extensive investigation into electrochemical applications. Herein, an amorphous phosphate-adsorbed and RuNi-doped molybdate (RuNiMo-P) composite is synthesized on nickel foam (NF) support by using a simple two-step method. Significantly, an acidic solution of phosphomolybdic acid (PMo12), containing a low concentration of Ru, can etch the NF, contributing to the in situ growth of the RuNi-doped molybdate precursor. Subsequent phosphating ensures the surface formation of the amorphous phosphate layer due to abundant oxygen in the precursor. The strong structural interaction between RuNi-doped molybdate and amorphous phosphate in RuNiMo-P prompts an enhanced hydrogen evolution reaction (HER) performance, delivering an overpotential of 38 mV at a current density of -10 mA cm-2, a Tafel slope of 53 mV dec-1, and good stability in an alkaline medium. Characterizations after HER reveal that RuNi doping, partial dissolution of phosphate and molybdate species, and newly formed NiOOH nanosheets can expose active sites, facilitate charge transfer, and modify electronic structures, thereby improving the HER performance effectively.

Unexpected Cu and Zn speciation patterns in the broiler feed-animal-excreta system revealed by XAS spectroscopy

Trace minerals such as copper (Cu) and zinc (Zn) are animal nutrition supplements necessary for livestock health and breeding performance, yet they also have environmental impacts via animal excretion. Here we investigated changes in Cu and Zn speciation from the feed additive to the broiler excreta stages. The aim of this study was to assess whether different Cu and Zn feed additives induce different Cu and Zn speciation patterns, and to determine the extent to which this speciation is preserved throughout the feed-animal-excreta system. Synchrotron-based X-ray absorption spectroscopy (XAS) was used for this investigation. The principal findings were: (i) in feed, Cu and Zn speciation changed rapidly from the feed additive signature (Cu and Zn oxides or Cu and Zn sulfates) to Cu and Zn organic complexes (Cu phytate and Zn phytate). (ii) in the digestive tract, we showed that Cu and Zn phytate were major Cu and Zn species; Cu sulfide and Zn amorphous phosphate species were detected but remained minor species. (iii) in fresh excreta, Cu sulfide and Zn amorphous phosphate were major species. These results should help to: (i) enhance the design of future research studies comparing different feed additive performances; (ii) assess Cu and Zn bioavailability in the digestive tract; (iii) gain further insight into the fate of Cu and Zn in cultivated soils when poultry manure is used as fertilizer.

Construction of NiCoP-NiCoO/NiCo–POx heterostructure by controllable phosphating effect for high-performance hybrid supercapacitors and alkaline zinc batteries

Heterostructures are enriched with interfacial effects from the separated materials with different chemical properties and crystal phases, which can be used to design advanced materials with novel properties. Besides, high-performance electroactive materials are still urgently needed for both hybrid supercapacitors (HSCs) and alkaline zinc batteries (AZBs), while single phase materials cannot meet comprehensive performance requirements of high-capacity, high-rate performance, and long-term cycling stability. Here, NiCoP-NiCoO2/NiCo−POx heterostructure is designed to achieve enriched interfacial effect between crystallized phosphides and amorphous phosphates. Our heterostructure is transformed from Ni1.5Co1.5O4 which is phosphatized using NaH2PO2·H2O, while this conversion method creates a great amounts of high-crystallized NiCoP nanoparticles which distributed in an amorphous NiCo−POx matrix. The heterostructure exhibits a high capacity of 177.0 mA h g–1 at 1 A g–1 and a high capacity retention of 125.0 mA h g–1 at 50 A g–1, combined with 78.7 % of capacity retention after 10,000 cycles. More significantly, NiCoP-NiCoO2/NiCo−POx heterostructure can be used as the cathode material for both HSCs and AZBs, and its excellent performance results in both high-energy and high-power performances in above two-type devices. Our investigations demonstrate excellent performance from the interfacial effect of our heterostructure, and give some insights to design advanced materials for energy storage applications.

Phosphate-based geopolymer: Influence of municipal solid waste fly ash introduction on structure and compressive strength

Materials resulting from incorporation of solid waste incineration fly ash into phosphate-based geopolymers, to partially replace metakaolin (up to 50% wt), were studied. X-ray diffraction, scanning electron microscopy, solid-state nuclear magnetic resonance spectroscopy and infrared spectroscopy were adopted to describe the mineralogical changes and the structural modifications of the geopolymer networks which impacted on the mechanical performance (compressive strength) of the materials. The results indicated that fly ash displays a different reactivity compared with metakaolin, behaving preferentially as a source of alkali that compete with the aluminosilicate metakaolin fraction by precipitating crystalline and amorphous phosphates. At 10 wt% of metakaolin substitution with fly ash, the extent and reticulation of the amorphous geopolymer matrix is preserved, and the mechanical properties are retained. At higher waste content (30–50% wt), the fast kinetics of the acid-base reactions involving the fly ash reactive phases prevail over the metakaolin dealumination, and the nature of the material shifts to an alkali-phosphate cement/phosphate-geopolymer composite. This behaviour, together with the development of porosity and presence of low-strength phases in the ash, led to a decline in the mechanical performance with increasing amount of substitution. All in all, this work provides fundamental information in the direction of a sustainable employment of phosphate-based geopolymers, which is limited by the relatively high cost of both metakaolin and phosphoric acid. Moreover, it indicates a recycling opportunity for this type of fly ash.

Optimization of Mn-Al-P Chemical Conversion Coating for a Process Sequence Adjusted Low Sn-Coated Steel

In recent years, in the field of tinplate production, it has become a trend to use lower tin coating mass to lower production costs. However, the preparation of low Sn-coated steel must face two significant problems: toxic chromate post-treatment and low corrosion resistance. In this work, we developed an Mn-Al-P chemical conversion coating using a process sequence-adjusted tinplate of 0.5 g/m2 tin coating mass as an alternative to the chromate treatment. Meanwhile, by adjusting the subsequence of the reflowing process and the post-treatment process, the wash water and electricity consumption were effectively reduced. The influence of reflowing time on the microstructural appearance, phase composition, surface element distribution, and corrosion resistance of this new brand tinplate was studied. Moreover, the composition was determined by x-ray photoelectron spectroscopy, and further discuss the formation mechanism of this coating. The results show that this mutielement coating could effectively fill tin-free zones on the surface of the tinplate and improve the corrosion resistance when the reflowing time is properly set up to 3.5 s after the process adjustment. However, continually extending the reflowing time would cause the phosphate coating to fall off, leading to the corrosion resistance deterioration. The coating was mainly made up of a series of amorphous phosphate compounds and metal oxides, which was suitable for a tinplate with low tin coating mass.

Differences of Enamel Microhardness Post External Bleaching After Application with Casein Phosphopeptide Amorphous Phosphate (CPP-ACP) and 5% Sodium Fluoride (NAF)

Background: Bleaching is an effort to lighten the color of teeth through the application of chemicals. One of the side effects of bleaching is that it causes demineralization so that the hardness of the enamel will decrease. The hardness of the enamel can be returned back through the mineral laying process, namely remineralization. Objective: The purpose of this study was to determine whether there were differences in post-bleaching enamel hardness after Casein Phosphopeptide Amorphous Phosphate (CPP-ACP) or 5% sodium fluoride (NaF) application. Methods: In this in-vitro research, bleaching was applied to 30 lower premolars that were divided into three groups, the first group without remineralization, the second group remineralization with CPP-ACP, and the third group remineralization with NAF. Enamel microhardness was measured using Vickers Hardness Tester Machine before bleaching, immediately after bleaching, after application of remineralization pastes, and after 7 days. The teeth were bleached with 40% hydrogen peroxide and underwent remineralization for 7 days. Results: The results showed differences in enamel microhardness after using CPP-ACP or 5% sodium fluoride (NaF) application, and the highest post-bleaching enamel hardness was after 5% NaF application. The data were analyzed and tested using ANOVA to measure the differences in hardness between more than 2 groups, and using the post hoc student t-test to measure the differences in violence between the 2 groups. Natural remineralization can occur with saliva but not optimally; therefore, additional remineralizing agents are needed. Conclusion: The conclusion of this study was that 5% NaF used as a remineralization agent after in-vitro bleaching could increase enamel microhardness more than CPP-ACP after 7 days of application.

Synergetic modulation on structure and interface enables bimetallic phosphide nanoarrays for advanced aqueous zinc batteries

Aqueous zinc batteries characterized by low-cost, high-capacity and high-safety are exciting for the energy storage sector, and the high-performance cathode plays a vital role for the commercialization. Herein, an in situ interfacial modification strategy is presented to construct high-performance cathode (N-NCP@POx) with ultrathin amorphous phosphate interfacial coating for alkaline zinc batteries. The in situ amorphous phosphate layers are beneficial to the adsorption and deprotonation of OH– confirmed by first-principles calculations, and are superior interfacial layers to protect the active species from passivation. This elaborate design enables the interface and structures synergistic effect endowing the electrode of N-NCP@POx with remarkable energy storage capability and electrochemical stability. As results, the full cell of N-NCP@POx//Zn alkaline zinc batteries deliver outstanding specific capacity (358.3 mAh/g at 1 A/g), rate performance (132.2 mAh/g at 20 A/g) and cyclic stability (94% retention after 6000 cycles at 10 A/g). This study will stimulate further development of transition metal phosphides with amorphous interface layers as high performance cathode for energy storage devices.

Differences of Enamel Microhardness Post External Bleaching After Application with Casein Phosphopeptide Amorphous Phosphate (CPP-ACP) and 5% Sodium Fluoride (NAF)

Background Bleaching is an effort to lighten the color of teeth through application of chemicals. One of the side effects of bleaching is that it cause demineralization so that the hardness of the enamel will decrease. The hardness of the enamel can be returned back through mineral laying process, namely remineralization. Objective: The purpose of this study was to determine whether there were differences in post-bleaching enamel hardness after Casein Phosphopeptide Amorphous Phosphate (CPP-ACP) or 5% sodium fluoride (NaF) application. Method: In this in-vitro research bleaching was applied to 30 lower premolars that were divided into three groups, the first group without remineralization, the second group remineralization with CPP-ACP, and the third group remineralization with NAF. Enamel microhardness was measured using Vickers Hardness Tester Machine before bleaching, immediately after bleaching, after application of remineralization pastes, and after 7 days. The teeth were bleached with 40% hydrogen peroxide and underwent remineralization for 7 days. Results: The results showed differences in enamel microhardness after using CPP-ACP or 5% sodium fluoride (NaF) application and the highest post-bleaching enamel hardness was after 5% NaF application. The data were analyzed and tested using ANOVA to measure the differences in hardness between more than 2 groups, and using the post hoc student t-test to measure the differences in violence between the 2 groups. Natural remineralization can occur with saliva but not optimally; therefore, additional remineralizing agents are needed. Conclusion: The conclusion of this study was that 5% NaF used as remineralization agent after in-vitro bleaching could increase enamel microhardness more than CPP-ACP, after 7 days of application.

Ornithogenesis and soil-landscape interplays at northern Harmony Point, Nelson Island, Maritime Antarctica.

Understanding the influence of soil-forming factors and processes in ornithogenic soils is important to predict impacts of climate change on Antarctic ecosystems. Herein, we analyzed the soil-landscape interplays and development of ornithogenic soils at Harmony Point (HP), Nelson Island. We collected, described, and classified 24 soil profiles, combined with vegetation and landforms descriptions. Geoprocessing techniques were employed for mapping. Soil physical, chemical, geochemical, and mineralogical analyses were applied. Patterned ground, "Ornithogenic"/Typic Gelorthent, and moss carpets were the dominant landform, soil and vegetation classes, respectively. Soils from rocky outcrops were more structured, acidic, with higher organic carbon, organometallic complexes, and secondary phosphate minerals, due to former bird influence. Soils from cryoplanated platforms presented higher water pH, base saturation, clay content, and secondary silicate minerals. Soils from marine terraces presented high exchangeable bases, phosphorous, and amorphous phosphate minerals. Soil chemical weathering is enhanced by ornithogenesis and widespread in HP. Besides ornithogenesis, organic matter accumulation, cryoturbation, and cryoclastic processes are also important to pedogenesis of ornithogenic soils. The soils of the cryoplanated platforms exhibited a gradient of pedogenetic development corresponding to increasing biota influence and distance from glacier. In contrast, soils of rocky outcrops were more developed even close to the glacier, due to ornithogenesis.

Phosphate induced formation of core-shell tin pyrophosphate via an acid method for proton conduction at elevated temperatures

Tin pyrophosphate is a feasible solid-state proton conductor as electrolyte and ionomers for applications in fuel cells and sensors, etc. Nevertheless, the morphology and proton conductivity of the SnP2O7 varies vigorously due to different fabrication methods, molar ratios of phosphorous to tin and sintering temperature. In this work, a core-shell SnP2O7 (c-SnP2O7) has been fabricated via a conventional acid method between SnO2 nanoparticles and various phosphoric acids including H3PO4, H4P2O7, (HPO3)x and P2O5 under temperature as low as 200 °C. The transformation of SnO2 to c-SnP2O7 in these phosphoric acids follows dissolving and reprecipitation mechanism where Sn(HPO4)2 is the intermediate species. In addition, the dominated factor for the transformation is the presence of P2O74− due to the condensation or hydration of various phosphoric acids. The as-synthesized c-SnP2O7 contains crystalline SnP2O7 inner core, an amorphous phosphate intermediate layer and an outer-layer with gel-like phosphorous-rich species. Furthermore, the phosphorous-rich gel layer contributes to outstanding proton conductivity of c-SnP2O7 up to 8.0 × 10−2 S cm−1 at 260 °C and excellent durability of 115 h at 240 °C and anhydrous conditions. Overall, the core-shell SnP2O7 is a promising proton conductor to be used in elevated temperature fuel cells.

Nanocrystalline Iron Pyrophosphate-Regulated Amorphous Phosphate Overlayer for Enhancing Solar Water Oxidation

HighlightsInducing a localized crystalline iron pyrophosphate in amorphous iron phosphate overlayer.Enhanced photoelectrochemical water oxidation activity with long-term durability.The heterogeneous hybrid structure overcoming the energy barrier in water oxidation.

Vascular calcification maladaptively participates in acute phosphate homeostasis.

Non-renal extravasation of phosphate from the circulation and transient accumulation into tissues and extracellular fluid is a regulated process of acute phosphate homeostasis that is not well understood. This process is especially relevant in the setting of chronic kidney disease (CKD), where exposure to increased phosphate is prolonged due to inefficient kidney excretion. Furthermore, CKD-associated mineral dysregulation induces pathological accumulation of phosphate causing vascular calcification (VC). Our objective was to determine whether the systemic response to acute phosphate challenges is altered by VC. After bolus phosphate administration, circulating and tissue deposition of this challenge was assessed in two rat models of VC using a radiolabelled phosphate tracer. In an adenine-induced model of CKD (N = 70), animals with VC had a blunted elevation of circulating 33PO4 following oral phosphate administration (P < 0.01), and the discordant deposition could be traced to the calcified arteries (11.4 [7.5-13.1] vs.43.0 [35.5-53.7] pmol/ng tissue, P < 0.001). In a non-CKD model of VC, calcification was induced with 0.5 ug/kg calcitriol and then withdrawn (N = 24). New phosphate uptake by the calcified vasculature correlated to the pre-existing burden of calcification (r = 38, P < 0.001) and was substantially attenuated in the absence of calcification stimulus (P < 0.01). Phosphate accrual was stimulated by the phosphate challenge and not present to the same degree during passive disposition of circulating phosphate. Further, the form of phosphate that deposited to the vasculature was predominately amorphous inorganic phosphate and not that which was bound in matured calciprotein particles. In the process of calcification, arteries acutely deposit substantial amorphous phosphate while blunting the elevation in the circulation, thereby altering the systemic disposition of phosphate and identifying VC as a participatory mineral homeostatic organ. This study demonstrates the negative vascular consequence of acute fluctuations in circulating phosphate, and supports the importance of phosphate bioavailability and diet management in CKD patients as a mediator of cardiovascular risk.

Evaluation of the Efficacy of CPP-ACP Remineralizing Mousse in MIH White and Yellow Opacities-In Vitro Vickers Microhardness Analysis.

Remineralization of tooth enamel can be partially achieved by the application of a casein phosphopeptides and amorphous phosphate (CPP-ACP) complex. However, evidence to support its effectiveness in Molar-incisor-hypomineralization (MIH)-affected teeth is scarce. The study’s aim is to evaluate the efficacy of CPP-ACP mousse in remineralizing MIH-affected enamel using a Vickers microhardness test. Two groups of enamel opacities of hypomineralized permanent teeth, white (group A) and yellow (group B) lesions (n = 14), went through a 28-day treatment protocol with GC Tooth Mousse. Before and after treatment, microhardness was measured in three different areas of each tooth (hypomineralized, transition, and outside the hypomineralized area). Data were analyzed using parametric and non-parametric tests with a significance of p < 0.05. The mean microhardness values increased in the hypomineralized and transition areas in both groups after the treatment protocol (in group A, 105.38 ± 11.70 to 158.26 ± 37.34; 123.04 ± 22.84 to 156.33 ± 35.70; in group B, 108.63 ± 14.66 to 143.06 ± 22.81; 132.55 ± 20.66 to 146.00 ± 12.88) and the differences pre/post-treatment were statistically significant within each group (p < 0.001 for both groups). Between groups, there was a statistically significant difference in the same areas (hypomineralized: p = 0.003; transition: p = 0.008) with a higher improvement in enamel hardness in group A. Topical application of CPP-ACP showed an increase in the physical strength of the hypomineralized and transition areas of MIH-affected enamel, likely due to an increase in mineral content.

In-vitro corrosion behaviors of extruded Mg–Ga alloys in alpha minimum essential medium

The in-vitro corrosion behaviors of extruded Mg–xGa (x = 1, 3, 5) alloys in alpha minimum essential medium (α-MEM) were investigated. The bilayer corrosion film was composed of an outer layer dominated by amorphous phosphates–carbonates and an inner layer dominated by MgO–Mg(OH)2. Pure Mg and Mg–1Ga exhibited low corrosion rates and homogeneous corrosion behaviors owing to the protection from the compact corrosion films. By contrast, Mg–3Ga and Mg–5Ga exhibited high corrosion rates and inhomogeneous corrosion behaviors owing to the bulky micro-galvanic corrosion caused by Mg5Ga2. Based on these results, possible corrosion models were developed.

Study on the mechanism of rapid formation of ultra-thick tribofilm by CeO2 nano additive and ZDDP

CeO2 nanoparticles are potential anti-wear additives because of their outstanding anti-wear and load-bearing capacity. However, the shear-sintering tribo-film formation mechanism of oxide nanoparticles limits the tribo-film formation rate and thickness greatly. In this study, by compounding with zinc dioctyl dithiophosphate (ZDDP), ultra-fine CeO2 nanoparticles modified with oleylamine (OM) can quickly form 2 µm ultra-thick tribo-film, which is 10–15 times thicker than that of ZDDP and CeO2, respectively. The ultra-thick tribo-film presents a nanocomposite structure with amorphous phosphate as binder and nano-CeO2 as filling phase, which leads to the highest loading capacity of composite additives. The results of adsorption experiments tested by dissipative quartz crystal microbalance (QCM-D) showed that the PB value of additive has nothing to do with its equilibrium adsorption mass, but is directly proportional to its adsorption rate in 10 s. The compound additive of CeO2 and ZDDP presented the co-deposition mode of ZDDP monolayer rigid adsorption and CeO2 viscoelastic adsorption on the metal surface, which showed the highest adsorption rate in 10 s. It is found that the tribo-film must have high film forming rate and wear resistance at the same time in order to achieve super thickness. Cerium phosphate was formed from ZDDP and CeO2 through tribochemistry reaction, which promotes the formation of an ultra-thick tribo-film with nanocomposite structure, which not only maintains the low friction characteristics of CeO2, but also realizes high PB and high load-carrying capacity.