Phosphide Nanoparticles Research Articles

Impact of Pre-Silica-Coating on the Luminescence Properties of Silica-Coated Indium Phosphide Nanoparticles

This study examined the impact of silica-coating on the luminescence characteristics of indium phosphide (InP) nanoparticles. Silica-coated InP nanoparticles were prepared using three different techniques. The first method utilized tetraethoxysilane (TEOS) as the silica source, resulting in the encapsulation of multiple InP nanoparticles within silica spheres. This approach caused a red-shift in the luminescence peak wavelength of the InP colloidal solution post-TEOS coating, compared to the original InP colloidal solution. Conversely, the second method employed tetramethoxysilane (TMOS), resulting in the formation of irregularly shaped silica-coatings on multiple InP nanoparticles, which reduced the red-shift in the luminescence peak wavelength of the silica-coated InP colloidal solution. The third method involved pre-coating InP nanoparticles with TMOS, followed by thickening the silica shells using TEOS. This technique successfully encapsulated multiple InP nanoparticles within silica spheres, maintaining the luminescence peak wavelength of the InP colloid solution post-coating with TMOS and TEOS nearly identical to that of the original solution. This method merged the advantageous outcomes of the first two methods. Additionally, silica spheres containing InP nanoparticles synthesized using both TMOS and TEOS exhibited the highest luminescence intensity. In summary, this study introduces a novel approach in nanoparticle engineering, enhancing the functional properties of InP nanoparticles and expanding their potential applications in optoelectronic devices.

Reinforcing the Efficiency of Plastic Upgrading through Full-Spectrum Photothermal Effect Integration of Heat Isolator.

Photoreforming of polyethylene terephthalate (PET) to H2 is practically attractive strategy for upgrading waste plastics. The major challenge is to utilize the infrared energy in the solar spectrum to improve the efficiency for photoreforming of PET to H2. Herein, through the ingenious integration of tungsten phosphide nanoparticles and tungsten single atoms (WP/W SAs) with carbon nitride (g-C3N4), the constructed hybrid inherits both the desirable properties and structural merits of the respective building blocks. Specifically, the photothermal effect of WP/W SAs couples with the "heat isolator" role of g-C3N4 due to its low thermal conductivity, thereby forming localized high-temperature regions, reducing the activation energy and improving the kinetics in the photoreforming of PET to H2. Additionally, the green pretreatment of PET using alkali-free hydrothermal strategy is reported, achieving direct separation of the ethylene glycol and terephthalic acid. This work not only provides an alkali-free hydrothermal pretreatment for PET, but also integrates the photothermal effect with the thermal insulation and opens a new avenue for harnessing solar energy into to convert plastics into H2.

Iron phosphide nanoparticles anchored on 3D nitrogen-doped graphene as an efficient electrocatalysts for hydrogen evolution reaction in alkaline media

Electrocatalysts play a crucial role in hydrogen evolution reaction (HER), facilitating a clean and sustainable generation of hydrogen energy. To promote the HER process, it is imperative to employ highly efficient, stable, and cost-effective electrocatalysts. This research focuses on the design of iron phosphide nanoparticles anchored onto a porous three-dimensional nitrogen-doped graphene (FeP@3DNG). The porous framework of 3DNG serves a multifaceted purpose: it prevents the aggregation of FeP nanoparticles during phosphidation, safeguards the FeP electrocatalyst from oxidation during the HER, and simultaneously enhances electrical conductivity and stability. Notably, the FeP@3DNG nanocomposite demonstrated the efficient activity and highest HER activity with an overpotential of 76 mV to achieve 10 mA cm−2 and a small Tafel slope of 40.2 mV dec−1 as well as good long-term durability for 20 h in 1.0 M KOH solution. The high performance of the FeP@3DNG nanocomposite can be primarily corresponded to the synergistic effects of the highly active of FeP nanoparticles and advantages of porous three-dimensional graphene with excellent electrocatalytic activity, high specific surface area, and chemical stability, thus, resulting in the improvement the overall electrocatalytic activity.

Hierarchical nickel phosphide/carbon nanofibers for high performance pseudocapacitors

Nickel phosphide (Ni3P)/Carbon nanofibers (CNFs) with controllable sizes and morphologies are synthesized using micro arc oxidation method combined with thermochemical vapor deposition, with adjustment of different annealing temperatures to control the dimension of CNFs. In this study, we report the in situ formation of transition metal phosphide nanoparticles through the conversion of 1D Ni5TiO7 nanowires. This fabrication strategy ensures the high growth density of CNFs. The initially formed Ni3P nanoparticles boost the catalytic growth of CNFs, which feature a high specific surface area and excellent conductivity. Together with redox electrolyte, the specific capacitance of Ni3P/CNFs based pseudocapacitor (PC) is 114.6 mF cm−2 at a scan rate of 10 mV s−1 and maintains 95.0 % of initial capacity after 10,000 cyclic charging/discharging test. Moreover, such composite based symmetric PCs offer an energy density of as high as 31.6 Wh kg−1 accompanied with a power density of 10.3 kW kg−1. The performance of formed PC devices is comparable to market-available (Li-/Na-) batteries. Therefore, Ni3P/CNFs composite film is a suitable capacitor electrode material for constructing high performance symmetric carbon material based PCs.

Dual modification of cobalt silicate nanobelts by Co3O4 nanoparticles and phosphorization boosting oxygen evolution reaction properties

Oxygen evolution reaction (OER) process is the “bottleneck” of water splitting, and the low-cost and high-efficient OER catalysts are of great importance and attractive but they are still challenging. Herein, a dual modification strategy is developed to tune and enrich the structure of cobalt silicate (Co2SiO4) showing boosted OER properties. Cobalt oxide (Co3O4) decorated Co2SiO4 nanobelts, denoted as CS, is firstly prepared using a Co-based precursor by a facile hydrothermal reaction. Then, cobalt phosphide (CoP) nanoparticles are in-situ grown on CS (denoted as CS-P) by the phosphorization process, which provide many active sites and boost the surface reactivity. The experimental results and density function theory (DFT) calculations both reveal that the CoP on CS can improve the conductivity and ensure fast kinetics, thus leading to boost the OER properties of Co2SiO4. When the phosphorization temperature is at 400 °C (CS-P400), it gains the lowest overpotential of 297 mV, which is much lower than CS (340 mV) and Co2SiO4 (409 mV) at 10 mA·cm−2, and even superior to the state-of-the-art transition metal silicates. CS-P400 also achieves high electrochemical active surface area (ECSA) and small Tafel slope owing to its porous structures with large specific surface area and nanosheet-like structures which are good for exposing many active sites and favorable to the fast kinetics. This work not only provides a dual modification route to boost catalytic activity of Co2SiO4 (CS-P400), but also sheds light on a new avenue for developing highly dispersed CoP on silicates to boost OER performances.

Synthesis of Amorphous and Various Phase-Pure Nanoparticles of Nickel Phosphide with Uniform Sizes via a Trioctylphosphine-Mediated Pathway.

Nickel phosphides are of particular interest because they are highly active and stable catalysts for petroleum/biorefinery and hydrogen production. Despite their significant catalytic potential, synthesizing various phase-pure nickel phosphide nanoparticles of uniform size remains a challenge. In this work, we develop a robust trioctylphosphine (TOP)-mediated route to make highly uniform phase-pure Ni12P5, Ni2P, and Ni5P4 nanoparticles. The synthetic route forms amorphous Ni70P30 nanoparticle intermediates. The reactions can be stopped at the amorphous stage when amorphous particles are desired. The amount of P incorporation can be controlled by varying the ratio of TOP to Ni(II). The mechanism for composition control involves the competition of the kinetics of two processes: the addition of the reduced Ni and the incorporation of P into Ni. Uniform Ni70P30 amorphous nanoparticles can be generated at a high TOP-to-Ni(II) ratio, where the P incorporation kinetics is made to dominate. Ni70P30 can later be transformed into phase-pure Ni12P5, Ni2P, and Ni5P4 nanocrystals of uniform size. The transformation can be controlled precisely by modulating the temperature. A UV-vis study coupled with theoretical modeling reveals Ni(0)-TOPx complexes along the synthetic path. This approach may be expanded to create other metal compounds, potentially enabling the synthesis of uniform nanoparticles of a greater variety.

Laser solid-phase synthesis of graphene shell-encapsulated high-entropy alloy nanoparticles

Rapid synthesis of high-entropy alloy nanoparticles (HEA NPs) offers new opportunities to develop functional materials in widespread applications. Although some methods have successfully produced HEA NPs, these methods generally require rigorous conditions such as high pressure, high temperature, restricted atmosphere, and limited substrates, which impede practical viability. In this work, we report laser solid-phase synthesis of CrMnFeCoNi nanoparticles by laser irradiation of mixed metal precursors on a laser-induced graphene (LIG) support with a 3D porous structure. The CrMnFeCoNi nanoparticles are embraced by several graphene layers, forming graphene shell-encapsulated HEA nanoparticles. The mechanisms of the laser solid-phase synthesis of HEA NPs on LIG supports are investigated through theoretical simulation and experimental observations, in consideration of mixed metal precursor adsorption, thermal decomposition, reduction through electrons from laser-induced thermionic emission, and liquid beads splitting. The production rate reaches up to 30 g/h under the current laser setup. The laser-synthesized graphene shell-encapsulated CrMnFeCoNi NPs loaded on LIG-coated carbon paper are used directly as 3D binder-free integrated electrodes and exhibited excellent electrocatalytic activity towards oxygen evolution reaction with an overpotential of 293 mV at the current density of 10 mA/cm2 and exceptional stability over 428 h in alkaline media, outperforming the commercial RuO2 catalyst and the relevant catalysts reported by other methods. This work also demonstrates the versatility of this technique through the successful synthesis of CrMnFeCoNi oxide, sulfide, and phosphide nanoparticles.

Ultrafast Synthesis of Transition Metal Phosphides in Air via Pulsed Laser Shock.

Transition metal phosphide nanoparticles (TMP NPs) represent a promising class of nanomaterials in the field of energy; however, a universal, time-saving, energy-efficient, and scalable synthesis method is currently lacking. Here, a facile synthesis approach is first introduced using a pulsed laser shock (PLS) process mediated by metal-organic frameworks, free of any inert gas protection, enabling the synthesis of diverse TMP NPs. Additionally, through thermodynamic calculations and experimental validation, the phase selection and competition behavior between phosphorus and oxygen have been elucidated, dictated by the redox potential and electronegativity. The resulting composites exhibit a balanced performance and extended durability. When employed as electrocatalysts for overall water splitting, the as-constructed electrolyzer achieves a low cell voltage of 1.54 V at a current density of 10 mA cm-2. This laser method for phosphide synthesis provides clear guidelines and holds potential for the preparation of nanomaterials applicable in catalysis, energy storage, biosensors, and other fields.

Facile Synthesis and Characterization of Copper Phosphide Nanoparticles as Efficient Electrocatalyst for Hydrogen and Oxygen Evolution Reaction

Facile Synthesis and Characterization of Copper Phosphide Nanoparticles as Efficient Electrocatalyst for Hydrogen and Oxygen Evolution Reaction

Synergistic heterostructural interface of CoP and WC for high-performance wide pH-universal hydrogen evolution electrocatalysis

The development of cost-effective catalysts with high activity and stability over a wide pH range is urgent, but there are great challenges in the selection and design of catalyst materials. In this work, cobalt phosphide nanoparticles were modified onto tungsten carbide nanowire arrays (CoP@WC/CC) on carbon cloth substrate by a two-step method. The construction of CoP@WC heterostructure results in the downward shift of the d-band center, which optimizes the adsorption energy of catalyst and reaction intermediates. Meanwhile, the synergistic effect of CoP and WC contributes to the alkaline HER kinetic process. In addition, binder-free self-supporting nanoarray have excellent electrical conductivity, large specific surface area and strong structure, which is conducive to charge/matter exchange and catalyst stability. The results show that CoP@WC/CC can effectively drive HER over a wide pH range and exhibit better catalytic performance than the single component control sample. In 0.5 M H2SO4 and 1 M KOH, CoP@WC/CC can drive the current density of 10 mA cm−2 with only 52 and 70 mV, while showing excellent stability without obvious performance degradation during 100 h of constant current test. A proton exchange membrane water electrolysis (PEMWE) using CoP@WC/CC catalyst operates stably for 200,000 s at 30 mA cm−2. This study provides a new reference for the design and development of high efficiency, low cost and wide pH-universal hydrogen evolution electrocatalysts.

Nickel phosphide: the Effect of Phosphorus Content on the Activity and Stability toward Oxygen Evolution Reaction in Alkaline Medium.

In this work, a systematic study of the effect of the metal to phosphorus ratio in Ni-P nanoparticles on their catalytic activity with respect to the OER is reported. To this end, nickel phosphide nanoparticles are synthesized through two different synthesis routes, one involving in-situ phosphidation and one involving ex-situ phosphidation. In-situ phosphidation is performed via two steps route in a one-pot synthesis, in which Ni nanoparticles are formed at 220 ◦C, but not isolated, and then transformed to phase pure either Ni12P5 or Ni2P nanocrystallites. In the second synthesis method (ex-situ phosphidation), nickel nanoparticles with an excess amount of trioctylphosphine (TOP) as a capping agent were synthesized and separated from the solution, then subsequently annealed in three different atmospheres, leading to the formation of three types of NixPy viz.[NixPy-H2/Ar], [NixPy-Ar], and [NixPy -air ], [NixPy -air ] nanoparticles showed the best electrocatalytic activity among the annealed nanoparticles in Ar and H2/Ar but lower than Ni12P5 nanoparticles. However, [NixPy -air ] showed very high stability in comparison with other synthesized nanoparticles. Moreover, the effect of the adventitious and spiked Fe in the electrolyte was studied on the electrocatalytic activity of all synthesized nanoparticles.

Size-controlled synthesis of cobalt phosphide (Co2P) nanoparticles and their application in non-enzymatic glucose sensors via a carbon fiber/Co2P composite

In this study, we synthesized Co2P nanoparticles using a solid-state phosphorization method and evaluated the electrocatalytic response to glucose oxidation reaction (GORs). The influence of synthesis conditions on the particle size, morphology of Co2P species and formation of byproducts is discussed. A lower molar ratio of the phosphorus precursor leads to a decrease in the generation of byproducts. In addition, the calcination temperature and time greatly influence the purity level of the Co2P species and its particle size. Thus, we obtained three pure Co2P nanoparticles with different sizes and morphologies. Significant differences in their electrocatalytic activity against the GOR are observed depending on the size of the particles, being the smaller ones the most efficient. Based on Tafel analysis, a higher catalytic activity was observed for the carbon fibre (CF)/Co2P composite compared to Co2P, which presented a greater onset potential and low response in current density. Tafel slopes close to 120 mV/dec were obtained for both materials, indicating that the mechanism is independent of the type of Co2P-based material used. Finally, the performance of the GCE/CF/Co2P sensor was demonstrated by amperometric measurements, with a sensitivity of 409 µAmM-1cm-2, a linear range between 39.4 µM and 150 µM, and a detection limit of 0.97 µM, analytical characteristics better than those obtained for other cobalt phosphide-based sensors reported in the literature. In addition, the GCE/CF/Co2P sensor shows excellent selectivity and demonstrated to be competitive compared to other Co-based non-enzymatic glucose sensors.

Construction of iron-doped nickel cobalt phosphide nanoparticles via solvothermal phosphidization and their application in alkaline oxygen evolution

Multi-metallic phosphides offer the possibility to combine the strategies of surface reconstruction, electronic interaction and mechanistic pathway tuning to achieve high electrocatalytic oxygen evolution activity. Here, iron-doped nickel cobalt phosphide nanoparticles (FexCoyNi2-x-yP) with the crystalline NiCoP phase are for the first time synthesized by the solvothermal phosphidization method via the reaction between metal–organic frameworks and white phosphorus. When used to electrochemically catalyze oxygen evolution reaction (OER), the Fe0.4Co0.8Ni0.8P supported by nickel foam requires only 248 mV overpotential to achieve 10 mA cm−2 current densities, and is robust towards the long-term OER in 1 M KOH. The higher number of electrochemically active sites can account for the good OER activity, along with the improved intrinsic activity which is caused by the electron interaction that optimizes the adsorption energy of hydroxyl intermediates, and that increases the acidity of high-valent metal centers. The OER mechanistic pathway involves both adsorbate and lattice oxygen. Surface conversion is observed after OER in alkaline solution, and metal phosphide layer transforms to metal oxides and (oxy)hydroxides.

A Rechargeable Solid-State Sodium-Oxygen Battery with Enhanced Energy Efficiency and Cycle Life

Sodium-oxygen (Na-O2) batteries offer a promising path for the advancement of high-energy-density inexpensive storage systems to replace current state of the art Li-based batteries owing to the natural abundance and low-cost Na metal. Despite numerous studies to improve the performance of liquid-based electrolyte Na-O2 batteries, this technology suffers from poor cycle life, electrolyte stability issues, and limited choice of cell design as well as growing safety concerns associated with liquid electrolytes. Recently, solid electrolytes received a great attention to substitute traditional liquid electrolytes used in Na-O2 batteries, due to their ability of improving safety and energy density. However, low ionic conductivity and high impedance in contact with the anode and cathode remain as major challenges for the development suitable solid-state electrolyte for Na-O2 batteries.In addressing these challenges, we recently have established a solid-state Na-O2 battery cell that comprises a highly conductive composite polymer-ceramic solid electrolyte with a conductivity of 0.7 mS/cm. This solid electrolyte works in synergy with vanadium phosphide (VP) nanoparticles, serving as oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) catalysts at the cathode and Na metal anode for more than 500 reversible charge-discharge cycles at a capacity of 1000 mAh/g, achieving a low polarization gap of approximately 20 mV in the first cycle. Various electrochemical and physicochemical characterization techniques, such as Raman spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), differential electrochemical mass spectrometry (DEMS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM), were employed to gain insight into the cell chemistry and solid-state electrolyte role in the formation and decomposition of sodium oxides components such as superoxide (NaO2), peroxide (Na2O2). The findings of this study underscore the significance of proper cell component design and possible mechanisms in solid-state Na-O2 battery technologies. This research represents a promising avenue in advancing energy conversion and storage systems, showcasing the potential of solid-state batteries with enhanced safety and performance characteristics.

Probing Mixed Phase Metallic Ni/Amorphous Nickel Phosphide Nanocatalysts during Oxygen Evolution Reaction Using Operando X-Ray Absorption Spectroscopy

Metal phosphide-containing nanomaterials have demonstrated remarkable efficacy as non-precious metal-based catalysts for the alkaline oxygen evolution reaction (OER). While it is widely acknowledged that various OER catalysts undergo structural reconstruction under applied OER potentials, monitoring these changes is challenging because they are often rapid and require instrumentation not typically found in the typical lab setting. In this study, we utilize operando X-ray absorption spectroscopy (XAS) to determine the structural reconstruction of nickel-based metal phosphide catalysts during OER. We have developed the synthesis of nickel-based phosphide nanoparticles with a range of phosphorus incorporation. These nanoparticles are composed of metallic nickel and amorphous nickel phosphide phases as determined by XRD, TEM and XAS. At low levels of P incorporation, from 2% to 15%, the synthesis results in the mixture of metallic nickel and amorphous phosphide phases. At higher levels of phosphorus incorporation, from 20% to 30%, amorphous nickel phosphide is the predominant phase. Electrochemical characterization of this nickel phosphide series for OER revealed that the catalysts with 20% phosphorus incorporation exhibited superior OER activity. The phosphides with lower phosphorus content, such as 2%, had smaller Ni2+/Ni3+ redox peaks which has been shown to suppress the conversion to Ni(OH)2, leading to lowered OER activity. Increased amorphous nickel phosphide phase led to greater activity, suggesting that the active component in the catalyst comes from the amorphous nickel phosphide phase. Meanwhile, higher phosphorus content (20-30%) where the amorphous phosphide is the predominate phase resulted in larger redox peaks, signifying greater conversion to Ni(OH)2. Operando XAS will be applied to investigate these metallic nickel/nickel phosphide nanocatalysts to elucidate their structural reconstruction during OER

Chalcogen-Based Precursors for Transition Metal (Co, Ni) Phosphides: (Di)chalcogenide-to-Phosphide Transformation via Chemical Extraction of Chalcogenides.

The chemical properties of polymorphic compounds are highly dependent on their stoichiometry and atomic arrangements, making certain phases technologically more important. Selective development of these phases is challenging. This study introduces a method where chalcogenide atoms from metal chalcogenides are chemically extracted by trioctylphosphine (TOP) and substituted with phosphide. Using this approach, dithiocarbamate/xanthate complexes of cobalt and nickel were employed for the selective synthesis of pure metal sulfides or phosphides. Optimization yielded either sulfur-deficient phases (Ni3S2, Co9S8) or a complete transformation to phosphides (Ni2P, CoP). Likewise, for the first time, selenobenzoate complexes of Ni and Co were used for the synthesis of transition metal diselenides (NiSe2, CoSe2), which could then be converted to metal phosphides (Ni2P, Co2P). The synthesis used solution-phase thermal decomposition with various precursors, surfactants, and temperatures. With TOP, different phases of metal chalcogenides, metal phosphides, and mixed metal phosphide nanomaterials (NiS, Ni3S2, Co9S8, NiSe2, CoSe2, Ni2P, Ni5P4, Co2P, CoP, and Ni2-xCoxP) were obtained by varying reaction conditions. The formation mechanism of nickel and cobalt phosphide nanoparticles from precursors is proposed, demonstrating that presynthesized metal chalcogenides can be transformed into phosphides, opening a new research avenue for dimensionally controlled metal chalcogenides as templates for metal phosphides.

Interface Engineering Induced N, P-Doped Carbon-Shell-Encapsulated FeP/NiP2/Ni5P4/NiP Nanoparticles for Highly Efficient Hydrogen Evolution Reaction

Modifying the electronic structure of a catalyst through interface engineering is an effective strategy to enhance its activity in the hydrogen evolution reaction (HER). Interface engineering is a viable strategy to enhance the catalytic activity of transition metal phosphides (TMPs) in the HER process. The interface-engineered FeP/NiP2/Ni5P4/NiP multi-metallic phosphide nanoparticles confined in a N, P-doped carbon matrix was developed by a simple one-step low-temperature phosphorization treatment, which only requires 72 and 155 mV to receive the current density of 10 mA/cm2 in acid and alkaline electrolyte, respectively. This enhanced performance can be primarily attributed to the heterointerface of FeP/NiP2/Ni5P4/NiP multi-metallic phosphides, which promotes electron redistribution and optimizes the adsorption/desorption strength of H* on the active sites. Furthermore, the N, P-doped carbon framework that encapsulates the nanoparticles inhibits their aggregation, leading to an increased availability of active sites throughout the reaction. The results of this study open up a straightforward and innovative approach to developing high-performance catalysts for hydrogen production.

Iron-Cobalt Phosphide Encapsulated in a N-Doped Carbon Framework as a Promising Low-Cost Oxygen Reduction Electrocatalyst for Zinc-Air Batteries.

The oxygen reduction reaction (ORR) plays a vital role in many next-generation electrochemical energy conversion and storage devices, motivating the search for low-cost ORR electrocatalysts possessing high activity and excellent durability. In this work, we demonstrate that iron-cobalt phosphide (FeCoP) nanoparticles encapsulated in a N-doped carbon framework (FeCoP@NC) represent a very promising catalyst for the ORR in alkaline media. The core-shell structured FeCoP@NC catalyst offered outstanding ORR activity with a half-wave potential (E1/2) of 0.86 V vs reversible hydrogen electrode (RHE) and excellent stability in a 0.1 M KOH electrolyte, outperforming commercial Pt/C and many recently reported noble-metal-free ORR electrocatalysts. The superiority of FeCoP@NC as an ORR electrocatalyst relative to Pt/C was further verified in prototype zinc-air batteries (ZABs), with the aqueous and flexible ZABs prepared using FeCoP@NC offering excellent stability, impressive open circuit voltages (1.56 and 1.44 V, respectively), and high maximum power densities (183.5 and 69.7 mW cm-2, respectively). Density functional theory calculations revealed that encapsulating FeCoP nanoparticles in N-doped carbon shells resulted in favorable electron penetration effects, which synergistically regulated the adsorption/desorption of ORR intermediates for optimal ORR performance while also boosting the electronic conductivity. Our findings offer valuable new insights for rational design of transition metal phosphide-based catalysts for the ORR and other electrochemical applications.

Synergistic rare-earth yttrium single atoms and copper phosphide nanoparticles for high-selectivity ammonia electrosynthesis

Synergistic rare-earth yttrium single atoms and copper phosphide nanoparticles for high-selectivity ammonia electrosynthesis

Sulfur-Tolerant Reductive Amination by Ruthenium Phosphide Nanoparticles Supported on Carbon

Sulfur-Tolerant Reductive Amination by Ruthenium Phosphide Nanoparticles Supported on Carbon