Atomically precise Ag_(30)Pd_(4)nanocluster as efficient polysulfides redox catalyst in Li-S batteries

Regulating the catalyst electronic structure is critical for improving the adsorption and catalytic conversion of lithium polysulfides(LiPSs)in lithium-sulfur batteries(Li-S),yet which has been overlooked in current studies.In this work,structurally defined Ag_(30)Pd_(4)nanoclusters were loaded onto reduced graphene oxide(Ag_(30)Pd_(4)/rGO)as a modification material for polypropylene(PP)separators to elucidate the catalytic activity towards lithium polysulfides and the impact on the electrochemical properties to lithium sulfur batteries.This unique d-πcombination promotes charge transfer,influences overall charge states,and further enhances adsorption energies in potential reaction pathways with lithium polysulfides.Consequently,the Ag_(30)Pd_(4)/rGO/PP modified batteries exhibited an exceptionally low-capacity decay rate of 0.026%per cycle at 1.0C over 1000 stable cycles and 9.75 mAh cm^(-2)excellent performance even with lean electrolyte and high sulfur loading(9.7 mg cm^(-2)).This study paves a path for employing ultrasmall bimetallic nanoclusters to promote the polysulfides redox kinetics hence boosting the lithiumsulfur battery performance.

Homoleptic alkynyl-protected Ag_(32 )nanocluster with atomic precision: Probing the ligand effect toward CO_(2) electroreduction and 4-nitrophenol reduction

We report a superatomic homoleptic alkynyl-protected Ag_(32)L_(24)(L=3,5-bis(trifluoromethylbenzene)acetylide,Ag_(32) for short)nanocluster with atomic precision,which possesses eight free electrons.Ag_(32) is formed by an Ag17 core with C3 symmetry and the remaining 15 Ag atoms bond to each other and coordinate with the 24 surface ligands.When applied as electrocatalyst for CO_(2) reduction reaction(CO_(2)RR),Ag_(32) exhibited the highest Faradaic efficiency(FE)of CO up to 96.44%at−0.8 V with hydrogen evolution being significantly suppressed in a wide potential range,meanwhile it has a reaction rate constant of 0.242 min−1 at room temperature and an activation energy of 45.21 kJ·mol−1 in catalyzing the reduction of 4-nitrophenol,both markedly superior than the thiolate and phosphine ligand co-protected Ag_(32) nanocluster.Such strong ligand effect was further understood by density functional theory(DFT)calculations,as it revealed that,one single ligand stripping off from the intact cluster can create the undercoordinated Ag atom as the catalytically active site for both clusters,but alkynyl-protected Ag_(32) nanocluster possesses a smaller energy barrier for forming the key*COOH intermediate in CO_(2)RR,and favors the adsorption of 4-nitrophenol.This study not only discovers a new member of homoleptic alkynyl-protected Ag nanocluster,but also highlights the great potentials of employing alkynyl-protected Ag nanoclusters as bifunctional catalysts toward various reactions.

Atomically precise alkynyl-protected Ag_(20)Cu_(12)nanocluster:Structure analysis and electrocatalytic performance toward nitrate reduction for NH_(3)synthesis

Electrochemical nitrate reduction reaction(NtrRR)has been emerging as an appealing route for both water treatment and NH_(3)synthesis.Herein,we report the structure analysis and electrocatalytic performance of a novel homoleptic alkynyl-protected Ag_(20)Cu_(12)nanocluster(Ag_(20)Cu_(12)in short)with atomic precision,which has eight free electrons and displays characteristic absorbance feature.Single crystal X-ray diffraction(SC-XRD)discloses that,it adopts a Ag_(14)kernel capped by three Ag_(2)Cu_(4)(C≡CArF)_(8)metal–ligand binding motifs in the outer shell.Ag_(20)Cu_(12)exhibited excellent catalytic performance toward NtrRR,as manifested by the superior NH_(3)Faradaic efficiency(FE,84.6%)and yield rate(0.138 mmol·h^(−1)·mg−1)than the homoleptic alkynyl-protected Ag_(32)nanoclusters.Additionally,it demonstrates good catalytic recycling capability.Density functional theory(DFT)calculations revealed that,the de-ligated Ag_(20)Cu_(12)cluster can expose the available AgCu bimetallic sites as the efficient active sites for NH_(3)formation.In particular,the participation of Cu sites greatly facilitates the initial capture of NO_(3)−and simultaneously promotes the selectivity of the final product.This study discovers a novel homoleptic alkynyl-protected AgCu superatom,and offers a great example to elucidate the structure–performance relationship of bimetallic catalyst for NtrRR and other multiple protons/electrons coupled electrocatalytic reactions.

Synthesis and structure of Au_(19)Ag_4(S-Adm)_(15) nanocluster:Polymorphs and optical properties

Polymorphism is a common phenomenon in nature.Here,we report one-pot wet chemical method to synthesize two polymorphs of Au_(19)Ag_(4)(S-Adm)_(15) nanocluster protected by 1-adamantanethiol(HSAdm),which adopt P-1 and P2_(1)/c space group respectively.The crystal structures of two polymorphs were determined by X-ray crystallography.Compared to the previously reported Au_(19)Ag_(4)(S-Adm)_(15)nanocluster adopting P2_(1)/n space group,polymorphs of Au_(19)Ag_(4)(S-Adm)_(15) with P-1 and P2_(1)/c space group show the different optical properties.Moreove r,Au_(19)Ag_(4)(S-Adm)_(15) with P-1 space group exhibits good thermal stability.Meanwhile,we investigated the effect of solvent and molar ratio of metal precursors on the polymorphs.This work provides an insight to polymorphs of metal nanoclusters.