The sluggish kinetics of oxygen reduction reaction(ORR)and oxygen evolution reaction(OER)have always restricted the development of lithium oxygen batteries(LOBs).Herein,hollow carbon spheres loaded with Pd/Pd_(4)S het...The sluggish kinetics of oxygen reduction reaction(ORR)and oxygen evolution reaction(OER)have always restricted the development of lithium oxygen batteries(LOBs).Herein,hollow carbon spheres loaded with Pd/Pd_(4)S heterostructure(Pd/Pd_(4)S@HCS)were successfully prepared via the in-situ deposition to improve the electrocatalytic activities for both ORR and OER in LOBs.With the welldispersed Pd/Pd_(4)S nanoparticles,the hierarchical composite with large specific surface area offers favorable transport channels for ions,electron and oxygen.Especially,the Pd/Pd_(4)S nanoparticles could exhibit excellent electrochemical performance for ORR and OER due to their intrinsic catalytic property and interfacial effect from the heterostructure.Therefore,the LOBs with Pd/Pd_(4)S@HCS as cathode catalyst show improved specific capacities,good rate ability and stable cycling performance.展开更多
Hollow nanostructures with structural advantages have been widely exploited as catalysts in electrochemical reactions.However,there are only limited strategies for constructing hollow Pd-based nanostructures.In this w...Hollow nanostructures with structural advantages have been widely exploited as catalysts in electrochemical reactions.However,there are only limited strategies for constructing hollow Pd-based nanostructures.In this work,Pd4S hollow nanospheres(Pd4S HNSs)are synthesized with a facile wet-chemical method via a self-templating process.Intermediate Pd-L-cysteine solid nanospheres(SNSs)were firstly obtained by the coordination of L-cysteine with Pd^(2+),and then in situ converted to hollow nanospheres in the following reduction process.The formation mechanism of the Pd4S HNSs was studied,and the size of the Pd4S HNSs can be readily adjusted by tuning the size of the SNSs.The hollow morphology would help the exposure of active sites and the prevention of aggregation during the catalytic reactions.As a result,the Pd4S HNSs exhibit improved catalytic performances in the oxygen reduction reactions,with a half-wave potential of 0.913 V vs.reversible hydrogen electrode(RHE)and impressive stability in the accelerated durability test.展开更多
基金supported by the Taishan Scholars Programme of Shandong Province(No.tsqn20161004)Project for Scientific Research Innovation Team of Young Scholar in Colleges and Universities of Shandong Province(No.2019KJC025)+1 种基金Young Scholars Program of Shandong University(No.2019WLJH21)China Postdoctoral Science Foundation(No.2020M672054)。
文摘The sluggish kinetics of oxygen reduction reaction(ORR)and oxygen evolution reaction(OER)have always restricted the development of lithium oxygen batteries(LOBs).Herein,hollow carbon spheres loaded with Pd/Pd_(4)S heterostructure(Pd/Pd_(4)S@HCS)were successfully prepared via the in-situ deposition to improve the electrocatalytic activities for both ORR and OER in LOBs.With the welldispersed Pd/Pd_(4)S nanoparticles,the hierarchical composite with large specific surface area offers favorable transport channels for ions,electron and oxygen.Especially,the Pd/Pd_(4)S nanoparticles could exhibit excellent electrochemical performance for ORR and OER due to their intrinsic catalytic property and interfacial effect from the heterostructure.Therefore,the LOBs with Pd/Pd_(4)S@HCS as cathode catalyst show improved specific capacities,good rate ability and stable cycling performance.
基金the National Natural Science Foundation of China(Nos.21703104,21673117,and 91956109)Nanjing Tech University(No.39837131).
文摘Hollow nanostructures with structural advantages have been widely exploited as catalysts in electrochemical reactions.However,there are only limited strategies for constructing hollow Pd-based nanostructures.In this work,Pd4S hollow nanospheres(Pd4S HNSs)are synthesized with a facile wet-chemical method via a self-templating process.Intermediate Pd-L-cysteine solid nanospheres(SNSs)were firstly obtained by the coordination of L-cysteine with Pd^(2+),and then in situ converted to hollow nanospheres in the following reduction process.The formation mechanism of the Pd4S HNSs was studied,and the size of the Pd4S HNSs can be readily adjusted by tuning the size of the SNSs.The hollow morphology would help the exposure of active sites and the prevention of aggregation during the catalytic reactions.As a result,the Pd4S HNSs exhibit improved catalytic performances in the oxygen reduction reactions,with a half-wave potential of 0.913 V vs.reversible hydrogen electrode(RHE)and impressive stability in the accelerated durability test.
