PDS (Phenyl disulfide, >99.0%) Powder as Electrolyte Additive for Battery and CO2RR, CBCO2RREAPDS
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Phenyl disulfide (also known as Diphenyl disulfide, Ph2S2) is an organosulfur compound that has emerged as a dual-purpose additive in carbon-based energy systems. In both CO2 reduction and Li-CO2 batteries, it functions primarily as a redox mediator and surface modifier, though its specific role shifts depending on the electrochemical environment.
As for Li-S batteries, phenyl disulfide acts as a chemical "scissor" to manage the "shuttle effect" and the sluggish kinetics of solid-state conversion. (1) Cleaving Polysulfides: Ph2S2 can undergo an exchange reaction with long-chain lithium polysulfides (Li2Sn). It cleaves the large molecules into smaller, more soluble organosulfur fragments (PhSnLi). (2) Improving Kinetics: By converting solid Li2S or Li2S2 into more soluble organolithium thiolates, it reduces the "dead sulfur" that typically accumulates on the cathode, improving capacity and rate performance. (3) Lowering Viscosity: The resulting organosulfur species often lead to a less viscous electrolyte compared to one saturated with inorganic polysulfides, facilitating faster ion transport.
Li-CO2 Batteries: As for Li-CO2 batteries, the primary challenge is the slow kinetics of the discharge product formation (Li2CO3) and its subsequent decomposition during charging. Phenyl disulfide acts as a Redox Mediator (RM). (1) Discharge (Oxygen/CO2 Reduction): Phenyl disulfide can help stabilize superoxide-like intermediates in the electrolyte. This promotes a solution-mediated pathway for the formation of Li2CO3, leading to large, crystalline discharge products rather than a thin, insulating film that "chokes" the cathode. (2) Charge (Oxygen/CO2 Evolution): The most critical role of Ph2S2 in Li-CO2 batteries is reducing the massive charging overpotential (often >4.0 V). The disulfide can be electrochemically oxidized at the cathode to form a radical cation or a thiosulfonate species. This oxidized species then chemically reacts with the solid Li2CO3 to decompose it, effectively acting as a "chemical catalyst" that lowers the voltage required to "clean" the cathode.
Electrochemical CO2 Reduction (CO2RR): In aqueous or organic CO2RR, phenyl disulfide is used to tune the selectivity of transition metal catalysts, particularly Copper (Cu) and Silver (Ag). (1) S-Metal Interaction: Phenyl disulfide can undergo reductive cleavage of the S-S bond at the cathode, forming thiolate species (PhS-) that chemisorb strongly onto the catalyst surface. (2) Selective Poisoning: This adsorbed layer "poisons" the active sites usually responsible for the Hydrogen Evolution Reaction (HER). By suppressing H2 production, the Faradaic Efficiency (FE) for carbon products (like CO or HCOO-) is significantly increased. (3) Electronic Effects: The sulfur atoms modify the d-band center of the metal catalyst. In some copper-based systems, this has been shown to stabilize the *CO intermediate, favoring C-C coupling and promoting the formation of Ethylene (C2H4).
| Part Number |
CBCO2RREAPDS (C-BCO2RR-EA-PDS) |
| CAS |
882-33-7 |
| Chemical Formula |
C6H5SSC6H5 ![]() |
| Appearance |
White powder |
| Purity |
>99.0% |
| Molecular Weight | 218.34 g/mol |
| Package Size | 50 g/bottle (250g, 1 kg, and 5 kg also can be supplied upon request) |
Notes: Please try to store the PDS powder in the dry place.
References:
- R. Pipes, et al. Phenyl Disulfide Additive for Solution-Mediated Carbon Dioxide Utilization in Li–CO2 Batteries, Adv Energy Mater., 2019, 9, 1900453.
- X. Zhang, et al. Promoting the conversion of Li2S by functional additives phenyl diselenide in Lithium–Sulfur batteries, J. Power Sources, 2021, 482, 228967.
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X. Li. Hoang, et al., Exploiting thiolate/disulfide redox couples toward large-scale electrochemical carbon dioxide capture and release, Energy Environ. Sci., 2025,18, 2584-2598.
