Sulfur Conversion Research Articles

Atom-Level Tandem Catalysis in Lithium Metal Batteries.

High-energy-density lithium metal batteries (LMBs) are limited by reaction or diffusion barriers with dissatisfactory electrochemical kinetics. Typical conversion-type lithium sulfur battery systems exemplify the kinetic challenges. Namely, before diffusing or reacting in the electrode surface/interior, the Li(solvent)x + dissociation at the interface to produce isolated Li+, is usually a prerequisite fundamental step either for successive Li+ "reduction" or for Li+ to participate in the sulfur conversions, contributing to the related electrochemical barriers. Thanks to the ideal atomic efficiency (100 at%), single atom catalysts (SACs) have gained attention for use in LMBs toward resolving the issues caused by the five types of barrier-restricted processes, including polysulfide/Li2S conversions, Li(solvent)x + desolvation, and Li0 nucleation/diffusion. In this perspective, the tandem reactions including desolvation and reaction or plating and corresponding catalysis behaviors are introduced and analyzed from interface to electrode interior. Meanwhile, the principal mechanisms of highly efficient SACs in overcoming specific energy barriers to reinforce the catalytic electrochemistry are discussed. Lastly, the future development of high-efficiency atomic-level catalysts in batteries is presented.

Electronic Spin Alignment within Homologous NiS2/NiSe2 Heterostructures to Promote Sulfur Redox Kinetics in Lithium-Sulfur Batteries.

The catalytic activation of the Li-S reaction is fundamental to maximize the capacity and stability of Li-S batteries (LSBs). Current research on Li-S catalysts mainly focuses on optimizing the energy levels to promote adsorption and catalytic conversion, while frequently overlooking the electronic spin state influence on charge transfer and orbital interactions. Here, hollow NiS2/NiSe2 heterostructures encapsulated in a nitrogen-doped carbon matrix (NiS2/NiSe2@NC) are synthesized and used as a catalytic additive in sulfur cathodes. The NiS2/NiSe2 heterostructure promotes the spin splitting of the 3d orbital, driving the Ni3+ transformation from low to high spin. This high spin configuration raises the electronic energy level and activates the electronic state. Thisaccelerates the charge transfer and optimizes the adsorption energy, lowering the reaction energy barrier of the polysulfidesconversion. Benefiting from these characteristics, LSBs based on NiS2/NiSe2@NC/S cathodes exhibit high initial capacity (1458 mAh·g⁻1 at 0.1C), excellent rate capability (572 mAh·g⁻1 at 5C), and stable cycling with an average capacity decay rate of only 0.025% per cycle at 1C during 500 cycles. Even at high sulfur loadings (6.2 mg·cm⁻2), high initial capacities of 1173 mAh·g⁻1 (7.27 mAh·cm⁻2) are measured at 0.1C, and 1058 mAh·g⁻1 is retained after 300 cycles.

ZnO enhanced molten Na2CO3-K2CO3 system for simulated waste resins treatment: Efficient conversion and fixation of organic sulfur and iron(III)

The radioactive spent resins from pressurized water nuclear power plant always contain a significant proportion of 55Fe, which invariably leads to the release of radionuclides and acidic gases if not treated promptly. Herein, an efficient ZnO enhanced molten salt oxidation (MSO) method was established for the removal and fixation of organic sulfur and Fe in simulated radioactive resins containing Fe3+ (Fe-CERs). The existence of Fe3+ facilitates the reaction with O2 to form Fe2O3, which contributes to the fracture of organic skeleton. The comparative study was conducted to explore the impact of ZnO on the oxidation behavior of Fe and S at 600–800 °C. The introduction of ZnO caused the continuous formation of ZnS at 600–700 °C, and the conversion of ZnO at 800 °C indirectly promotes the retention rate of S (85.42 %). The potential conversion of Zn0.73Fe0.27S to ZnS may occur within the temperature range of 700 °C to 800 °C. Additionally, the predominant presence of carbon in residues at approximately 700 °C could exert a stimulating effect on the sulfidation process of Fe2O3 and inhibit the formation of SO2. The coexistence of Fe2O3, carbon and ZnO effectively diminishes H2S and SO2 amounts while further enhancing the fixation of S and Fe. The increase generation of K2SO4, FeS and Fe3O4 leads to a high formation rate of SO42- (79.36 %) and a great retention efficiency of Fe (96.23 %) at 800 °C. The proposed novel MSO method holds promising potential for applications in the treatment of organic contaminants.

Procedures from samples to sulfur isotopic data: A review.

Sulfur isotopes have been widely used to solve some key scientific questions, especially in the last two decades with advanced instruments and analytical schemes. Different sulfur speciation and multiple isotopes analyzed in laboratories worldwide and in situ microanalysis have also been reported in many articles. However, methods of sampling to measurements are multifarious, and occasionally some inaccuracies are present in published papers. Vague methods may mislead newcomers to the field, puzzle readers, or lead to incorrect data-based correlations. We have reviewed multiple methods on sulfur isotopic analyses from the perspectives of sampling, laboratory work, and instrumental analysis in order to help reduce operational inhomogeneity and ensure the fidelity of sulfur isotopic data. We do not deem our proposed solutions as the ultimate standard methods but as a lead-in to the overall introduction and summary of the current methods used. It has been shown that external contamination and transformation of different sulfur species should be avoided during the sampling, pretreatment, storage, and chemical treatment processes. Conversion rates and sulfur isotopic fractionations during sulfur extraction, purification, and conversion processes must be verified by researchers using standard or known samples. The unification of absence of isotopic fractionation is needed during all steps, and long-term monitoring of standard samples is recommended. This review compiles more details on different methods in sampling, laboratory operation, and measurement of sulfur isotopes, which is beneficial for researchers' better practice in laboratories. Microanalyses and molecular studies are the frontier techniques that compare the bulk sample with the elemental analysis/continuous flow-gas source stable isotope ratio mass spectrometry method, but the latter is widely used. The development of sulfur isotopic measurements will lead to the innovation in scientific issues with sulfur proxies.

Room temperature, ultrafast and one-step synthesis of highly fluorescent sulfur quantum dots probe and their logic gate operation

The direct and rapid conversion of abundant and cheap elemental sulfur into fluorescent sulfur quantum dots (SQDs) at room temperature is a critical and urgent challenge. Conventional synthesis methods require high temperatures, high pressures, or specific atmospheric conditions, making them complex and impractical for real applications. Herein, we propose a simple method for synthesizing SQDs simply by adding H2O2 to an elemental sulfur-ethylenediamine (S-EDA) solution at room temperature. Remarkably, within a mere 10 min, SQDs with a photoluminescence quantum yield of 23.6 % can be obtained without the need for additional steps. A comprehensive analysis of the mechanism has demonstrated that H2O2 is capable of converting Sx2− ions generated in the S-EDA solution into zero-valent sulfur atoms through oxidation. The obtained SQDs can be utilized as a fluorescent probe for detection of tetracycline (TC) and Ca2+ ions with the limit of detection (LOD) of 0.137 μM and 0.386 μM respectively. Moreover, we have developed a sensitive logic gate sensor based on SQDs, harnessing the activated cascade effect to create an intelligent probe for monitoring trace levels of TC and Ca2+ ions. This paper not only presents a viable approach for ultrafast and scalable synthesis of SQDs at room temperature, but also contributes to the efficient utilization of elemental sulfur resources.

Highly Conductive Quasi‐1D Hexagonal Chalcogenide Perovskite Sr8Ti7S21 with Efficient Polysulfide Regulation in Lithium‐Sulfur Batteries

AbstractLithium‐sulfur batteries (LSBs) are regarded as one of the most promising candidates for next‐generation energy storage systems. However, the commercialization of LSBs is still hindered by several technical issues, including the notorious polysulfide migration from the cathode to the anode and the sluggish sulfur conversion kinetics. Herein, a quasi‐1D hexagonal chalcogenide perovskite, Sr8Ti7S21, is demonstrated as an efficient sulfur host able to overcome these limitations. Experimental results and density functional theory calculations show Sr8Ti7S21 to offer strong lithium polysulfides (LiPS) binding through multiple bond formation. Besides, Sr8Ti7S21 effectively facilitates the kinetics of the LiPS redox reaction. As a result, S@Sr8Ti7S21‐based cathodes exhibit excellent initial capacities up to 1315 mAh g−1 at 0.2C, impressive cycling stability with an average capacity decay rate of 0.08% per cycle over 400 cycles at 1C, and a high areal capacity of 6.58 mAh cm−2 under a high sulfur loading of 6.5 mg cm−2. This work reveals the potential capabilities and promising prospects of chalcogenide perovskites in advancing LSBs technology.

In situ TEM study of structure evolution of porous hollow carbon sphere/sulfur cathodes

Great progresses on improving capability and stability of lithium-sulfur batteries (LSBs) by developing novel electrodes and electrolytes have been achieved. However, the study on the electrochemical conversion of sulfur with their volume expansion is limited, but provides another promising approach to further promote the practical application of LSBs. Herein, we successfully synthesize porous hollow carbon spheres as the host for sulfur in LSBs. In situ transmission electron microscopy (TEM) is applied to track the real-time morphological and structural evolutions of the porous hollow carbon sphere/sulfur composite when lithiation occurs. A small volume expansion of 39.4% from its original state is observed, benefiting from the highly porous structure of carbon. As a result, the composite electrode achieves a high residual capacity of 712 mAh g−1 after 200 cycles.

A Lewis Acid–Lewis Base Hybridized Electrocatalyst for Roundtrip Sulfur Conversion in Lithium–Sulfur Batteries

AbstractElectrocatalysts can optimize the sulfur/sulfide reaction kinetics in Li–S batteries to compete with the loss of lithium polysulfides (LiPSs) caused by the shuttling effect. However, the design rationale of electrocatalysts to drive roundtrip sulfur/sulfide conversion is lacking. Here, pairing Lewis acidic and Lewis basic active sites to reach collective adsorption of LiPSs and simultaneous activation of electrophiles and nucleophiles in LiPSs is proposed. This concept is validated by doping polyaniline with protonated metatungstate anions, which enables reduced activation energies for both sulfur reduction reaction and sulfide oxidation reaction and results in significantly improved kinetics. Such electrocatalysts enable a Li–S battery to reach a low capacity‐decay rate of 0.029% per cycle for 1000 cycles. This work would offer insights into battery technologies where sulfur electrocatalysis will play pivotal roles.

Engineering Spin State in Spinel Co3O4 nanosheets by V‐Doping for Bidirectional Catalysis of Polysulfides in Lithium–Sulfur Batteries

AbstractThe slow bidirectional conversion and fast shuttling of lithium polysulfides (LiPSs) remain the main obstacles that inhibit the practical application of lithium sulfur batteries (LSBs). Here, by engineering the in‐spin state of spinel oxides, V doping‐induced hexagonal nanosheets (V‐Co3O4 NS) with intermediate spin state (IS, t2g5 eg1) can form stable bond order toward LiS* based on the ligand field theory and molecular orbital theory, thus effectively accelerating the sulfur conversion kinetics. Owing to these merits, the V‐Co3O4 NS modified separator base battery achieves a high areal capacity of 15.37 mAh cm−2 with sulfur loading of 15.4 mg cm−2, and it displays a low‐capacity attenuation of 0.015% each cycle at 3.0 C for 1900 cycles.

Quasi-Solid Sulfur Conversion for Energetic All-Solid-State Na-S Battery.

The high theoretical energy density (1274 Wh kg-1) and high safety enable the all-solid-state Na-S batteries with great promise for stationary energy storage system. However, the uncontrollable solid-liquid-solid multiphase conversion and its associated sluggish polysulfides redox kinetics pose a great challenge in tunning the sulfur speciation pathway for practical Na-S electrochemistry. Herein, we propose a new design methodology for matrix featuring separated bi-catalytic sites that control the multi-step polysulfide transformation in tandem and direct quasi-solid reversible sulfur conversion during battery cycling. It is revealed that the N, P heteroatom hotspots are more favorable for catalyzing the long-chain polysulfides reduction, while PtNi nanocrystals manipulate the direct and full Na2S4 to Na2S low-kinetic conversion during discharging. The electrodeposited Na2S on strongly coupled PtNi and N, P-codoped carbon host is extremely electroreactive and can be readily recovered back to S8 without passivation of active species during battery recharging, which delivers a true tandem electrocatalytic quasi-solid sulfur conversion mechanism. Accordingly, stable cycling of the all-solid-state soft-package Na-S pouch cells with an attractive specific capacity of 876 mAh gS -1 and a high energy of 608 Wh kgcathode -1 (172 Wh kg-1, based on the total mass of cathode and anode) at 60 °C are demonstrated.

One-pot synthesis of regenerative calcium counterions from waste chicken eggshells for SO2-to-sulfur reduction

Abating sulfur dioxide (SO2) emissions is increasingly critical for addressing environmental concerns and safeguarding human health. In this study, we propose a novel, sustainable approach utilizing in situ eggshell waste-derived calcium-based materials for the catalytic thermal reduction of SO2 to elemental sulfur. Our research focuses on the facile synthesis of calcium-based compounds, proceeding from chicken eggshells to CaO, CaSO4, and finally CaS, for treating hazardous SO2 gas in a one-pot reactor. The effects of gas hourly space velocity (GHSV), temperature, and catalyst stability were studied. Optimal conditions for sulfur yield (71.32%) and SO2 conversion (43.38%) were achieved at 800 °C with a GHSV of 117 L h/g. Our findings demonstrate that the calcium-based materials exhibit exceptional stability, maintaining activity for 6.5 h. Mechanistically, the synergistic pathways of Mars-Van Krevelen and Eley-Rideal mechanisms underlying the SO2 reduction process were elucidated. This research presents a sustainable solution for converting SO2 into a valuable sulfur commodity, and contributes to achieving Sustainable Development Goal No. 12 on Sustainable Consumption and Production. By harnessing CaS derived from eggshell waste, our work underscores the potential for environmentally friendly practices in addressing industrial emissions and advancing sustainable resource utilization.

Short-Chain Sulfur Confined into Nitrogen-Doped Hollow Carbon Nanospheres for High-Capacity Potassium Storage.

Carbon-based materials are one of the ideal negative electrode materials for potassium ion batteries. However, the limited active sites and sluggish diffusion ion kinetics still hinder its commercialization process. To address these problems, we design a novel carbon composite anode, by confining highly reactive short-chain sulfur molecules into nitrogen-doped hollow carbon nanospheres (termed SHC-450). The formation process involves the controlled synthesis of hollow polyaniline (PANI) nanospheres as precursors via an Ostwald ripening mechanism and subsequent sulfuration treatment. The high content of constrained short-chain sulfur molecules (20.94 wt%) and considerable N (7.15 wt%) ensure sufficient active sites for K+ storage in SHC-450. Accordingly, the SHC-450 electrode exhibits a high reversible capacity of 472.05 mAh g-1 at 0.1 A g-1 and good rate capability (172 mAh g-1 at 2 A g-1). Thermogravimetric analysis shows that SHC-450 has impressive thermal stability to withstand a high temperature of up to 640 °C. Ex situ spectroscopic characterizations reveal that the short-chain sulfur provides high capacity through reversible formation of K2S. Moreover, its special hollow structure not only provides ample space for highly active short-chain sulfur reactants but also effectively mitigates volume expansion during the sulfur conversion process. This work offers new perspectives on enhanced K+ storage performance from an interesting anode design and the space-limited domain principle.

Co-Fe dual-atom isolated in N-doped graphydine as an efficient sulfur conversion catalyst in Li-S batteries

Lithium-sulfur (Li-S) batteries have garnered considerable attention as a prospective energy storage device for the future due to their exceptionally high theoretical energy density. Unfortunately, sluggish sulfur reactions create a bottleneck in Li–S batteries, hindering their ability to deliver all their promised energy. In this work, we reported the N-doped graphydine as a sulfur host in a Li-S battery cathode. The graphydine host is decorated with isolated cobalt/iron dual-atom catalyst. Co/Fe sites in Li–S batteries play a double role as an electrocatalyst, speeding up the two-way conversion between sulfur and lithium sulfide during the battery's cycle. These composite electrocatalysts, built with a remarkable 70 wt% sulfur content, achieve a high specific capacity of 1520 mA h g⁻¹ at a low charging current density (0.1 C). At a low current density of 0.1 C, they present remarkable cycling consistency, losing only 0.07% of capacity for each cycle for 1000 cycles.

Quasi‐Solid Sulfur Conversion for Energetic All‐Solid‐State Na−S Battery

AbstractThe high theoretical energy density (1274 Wh kg−1) and high safety enable the all‐solid‐state Na−S batteries with great promise for stationary energy storage system. However, the uncontrollable solid–liquid‐solid multiphase conversion and its associated sluggish polysulfides redox kinetics pose a great challenge in tunning the sulfur speciation pathway for practical Na−S electrochemistry. Herein, we propose a new design methodology for matrix featuring separated bi‐catalytic sites that control the multi‐step polysulfide transformation in tandem and direct quasi‐solid reversible sulfur conversion during battery cycling. It is revealed that the N, P heteroatom hotspots are more favorable for catalyzing the long‐chain polysulfides reduction, while PtNi nanocrystals manipulate the direct and full Na2S4 to Na2S low‐kinetic conversion during discharging. The electrodeposited Na2S on strongly coupled PtNi and N, P‐codoped carbon host is extremely electroreactive and can be readily recovered back to S8 without passivation of active species during battery recharging, which delivers a true tandem electrocatalytic quasi‐solid sulfur conversion mechanism. Accordingly, stable cycling of the all‐solid‐state soft‐package Na−S pouch cells with an attractive specific capacity of 876 mAh gS−1 and a high energy of 608 Wh kgcathode−1 (172 Wh kg−1, based on the total mass of cathode and anode) at 60 °C are demonstrated.

Strengthening d‐p Orbital‐Hybridization via Coordination Number Regulation of Manganese Single‐Atom Catalysts Toward Fast Kinetic and Long‐Life Sodium–Sulfur Batteries

AbstractThe practical application of room‐temperature sodium‐sulfur (RT Na–S) batteries is blocked by the notorious shuttle effect of sodium polysulfides (NaPSs) and sluggish refox reaction kinetics. Single‐atom catalysts (SACs) have been widely studied for boosting the energy storage performance of RT Na‐S batteries. Nevertheless, the catalytic centers of SACs reported so far have focused mainly on symmetrical metal–N4 structures, which offer weak bonding affinity toward polar NaPSs, leading to detrimental shuttle effect and sluggish sulfur conversion kinetics. Herein, a novel asymmetrical Mn–N2 structure is implanted into nitrogen‐doped carbon nanofibers (Mn‐N2/CNs) through thermal NH3 etching of a symmetrical Mn–N2O2 structure. The Mn–N2 structure promotes the bonding affinity and catalytic conversion of NaPSs due to the strengthened d‐p orbital‐hybridization between the d orbital of Mn in the Mn–N2 structure and the p orbital of S in NaPSs. Consequently, Mn‐N2/CNs@S achieves a high capacity of 458 mAh g−1 at 3.0 C with a capacity decay of 0.23% over 2300 cycles. This work offers a promising pathway for regulating the coordination number of SACs with strengthened d‐p orbital‐hybridization for high‐performance RT Na–S batteries.

The impact of reduced sulfur compounds on aerobic granular sludge formation and biological phosphorus removal

Biological sulfur conversion combined with phosphorus removal represents an innovative biotechnology for activated sludge (AS). However, its effect on the formation of aerobic granular sludge (AGS) remains unclear. This study aimed at determining the impact of sulfide and thiosulfate on the performance of enhanced biological phosphorus removal (EBPR) and on AGS formation. Using two lab-scale sequencing batch reactors (SBR), we compared EBPR performance, the degree of granulation, and the enriched microbial community with sulfide (SBR-S, 20 mg S/L) or thiosulfate (SBR-T, 140 mg S/L) as primary sulfur source. Results indicate that both reactors achieved comparable EBPR performance, with a phosphorus removal rate of 98% in SBR-T and 99% in SBR-S. SBR-T resulted in compact granules with fast settling properties, while SBR-S resulted in dense floccular sludge, referred to as “densified sludge”. Both systems enriched a comparable microbial community with shared dominant genera, including Ca. Competibacter, Thiothrix, Ca. Accumulibacter and Dechloromonas. The higher abundance of Thiothrix unzii throughout the operating time in SBR-T, reaching 19.4%, is believed to have enhanced the granulation process. This study provides important insight into the role of reduced sulfur compounds in sludge densification and EBPR performance, relevant to sulfur-rich wastewaters such as those from industrial sources.

Synergetic catalytic regulation of nitrogen doped NiS2/CoS2 heterostructure for polysulfide immobilization in Li-S batteries

The sluggish kinetics of sulfur species conversion and the shuttle effect in lithium-sulfur batteries are severely hindered in practical applications. Herein, we propose nitrogen doped NiS2/CoS2 heterostructure supported on CNT (N-NiS2/CoS2/CNT) by simple thiourea pyrolysis served as electrocatalyst functionalized on PP separator. The new formed M-N bonds on N-NiS2/CoS2/CNT motivate the catalytic activity of metal active centers strengthening the chemical anchoring towards polysulfides and Li2S electrodeposition behavior. The N,S dual doping on CNT support synergistically affords the electrochemical active sites for polysulfides conversion kinetics and increases the electrical conductivity of the whole catalyst. In Li-S batteries, the initial capacity of the battery with N-NiS2/CoS2/CNT functionalized separators reaches 1317.3 mAh g−1 at 0.2 C, and after 200 cycles, the capacity reaches 939.5 mAh g−1 with a capacity retention rate of 59.8%. Even at a large multiplicity rate of 2 C, the capacity can still be maintained at 552.2 mAh g−1 with a low-capacity decay of 0.068% after 500 cycles.

Catalytic Solid‐State Sulfur Conversion Confined in Micropores toward Superhigh Coulombic Efficiency Lithium‐Sulfur Batteries

AbstractAchieving the solid–solid conversion of sulfur is a fundamental solution to eliminating the shuttling of soluble polysulfides and improving the cycling stability of lithium‐sulfur batteries. However, the sluggish solid reaction kinetics seriously challenge the battery performance. In this work, a micropore‐confined catalysis strategy to achieve the smooth solid–solid conversion of sulfur is proposed. It is realized by storing sulfur in a microporous carbon host with narrow pore size and uniformly distributed single‐atom Co catalytic sites. The microporous structure avoids the contact of electrolyte solvents with the inner sulfur, preventing the formation and dissolution of polysulfides and efficiently suppressing sulfur loss during cycling. The introduced single‐atom Co catalytic sites promote the charge transfer to accelerate the solid–solid conversion of sulfur. When coupled with a liquid carbonate electrolyte, the battery exhibits a remarkably high Coulombic efficiency (CE) of ≈99.88% and a minimal capacity decay rate of ≈0.016% per cycle for 1000 cycles at 0.5 C. Even when coupled with the solid‐state electrolyte, the battery still delivers a significantly high capacity of 1100 mAh g−1 and a remarkably high CE of ≈99.83% over 200 cycles. This work reveals a promising solution for developing practical stable Li─S batteries.

Multifunctional Heterostructured Fe3O4-FeTe@MCM Electrocatalyst Enabling High-Performance Practical Lithium-Sulfur Batteries Via Built-in Electric Field.

The development of capable of simultaneously modulating the sluggish electrochemical kinetics, shuttle effect, and lithium dendrite growth is a promising strategy for the commercialization of lithium-sulfur batteries. Consequently, an elaborate preparation method is employed to create a host material consisting of multi-channel carbon microspheres (MCM) containing highly dispersed heterostructure Fe3O4-FeTe nanoparticles. The Fe3O4-FeTe@MCM exhibitsa spontaneous built-in electric field (BIEF) and possesses both lithophilic and sulfophilic sites, rendering it an appropriate host material for both positive and negative electrodes. Experimental and theoretical results reveal that the existence of spontaneous BIEF leads to interfacial charge redistribution, resulting in moderate polysulfide adsorption which facilitates the transfer of polysulfides and diffusion of electrons at heterogeneous interfaces. Furthermore, the reduced conversion energy barriers enhanced the catalytic activity of Fe3O4-FeTe@MCM for expediting the bidirectional sulfur conversion. Moreover, regulated Li deposition behavior is realized because of its high conductivity and remarkable lithiophilicity. Consequently, the battery exhibited long-term stability for 500 cycles with 0.06% capacity decay per cycle at 5 C, and a large areal capacity of 7.3mAhcm-2 (sulfur loading: 9.73mgcm-2) at 0.1 C. This study provides a novel strategy for the rational fabrication of heterostructure hosts for practical Li-S batteries.

A Synthetic Microbiome Based on Dominant Microbes in Wild Rice Rhizosphere to Promote Sulfur Utilization

Sulfur (S) is one of the main components of important biomolecules, which has been paid more attention in the anaerobic environment of rice cultivation. In this study, 12 accessions of rice materials, belonging to two Asian rice domestication systems and one African rice domestication system, were used by shotgun metagenomics sequencing to compare the structure and function involved in S cycle of rhizosphere microbiome between wild and cultivated rice. The sulfur cycle functional genes abundances were significantly different between wild and cultivated rice rhizosphere in the processes of sulfate reduction and other sulfur compounds conversion, implicating that wild rice had a stronger mutually-beneficial relationship with rhizosphere microbiome, enhancing sulfur utilization. To assess the effects of sulfate reduction synthetic microbiomes, Comamonadaceae and Rhodospirillaceae, two families containing the genes of two key steps in the dissimilatory sulfate reduction, aprA and dsrA respectively, were isolated from wild rice rhizosphere. Compared with the control group, the dissimilatory sulfate reduction in cultivated rice rhizosphere was significantly improved in the inoculated with different proportions groups. It confirmed that the synthetic microbiome can promote the S-cycling in rice, and suggested that may be feasible to construct the synthetic microbiome step by step based on functional genes to achieve the target functional pathway. In summary, this study reveals the response of rice rhizosphere microbial community structure and function to domestication, and provides a new idea for the construction of synthetic microbiome.