物理化学学报
物理化學學報
물이화학학보
ACTA PHYSICO-CHIMICA SINICA
2015年
1期
111-120
,共10页
苏硕剑%努丽燕娜%非路热·吐尔逊%杨军%王久林
囌碩劍%努麗燕娜%非路熱·吐爾遜%楊軍%王久林
소석검%노려연나%비로열·토이손%양군%왕구림
可充镁电池%正极%集流体%电化学性能%腐蚀
可充鎂電池%正極%集流體%電化學性能%腐蝕
가충미전지%정겁%집류체%전화학성능%부식
Rechargeable magnesium battery%Cathode%Current collector%Electrochemical performance%Corrosion
以目前常用的Chevrel相Mo6S8作为正极材料,涂覆在不同集流体(不锈钢、镍、铜、钛)上,以镁为负极,研究了在(PhMgCl)2-AlCl3/四氢呋喃(简称THF)“二代”电解液中集流体对可充镁电池电化学性能的影响。恒流放电-充电结果显示在不锈钢集流体上电池电压极化最小,并且具有较好的循环稳定性;镍、铜次之;钛集流体上的极化最大,循环稳定性也最差。并通过对比放电-充电循环前后电极和集流体表面的微观结构,探讨了集流体对电池性能显著影响的原因。电解液对集流体会造成腐蚀,不同集流体在电解液中的稳定性有差异;正极材料涂覆在不同集流体上,电极表面状况有差异;负载活性材料后集流体发生腐蚀的电位有所降低,使集流体更易受到电解液的腐蚀。
以目前常用的Chevrel相Mo6S8作為正極材料,塗覆在不同集流體(不鏽鋼、鎳、銅、鈦)上,以鎂為負極,研究瞭在(PhMgCl)2-AlCl3/四氫呋喃(簡稱THF)“二代”電解液中集流體對可充鎂電池電化學性能的影響。恆流放電-充電結果顯示在不鏽鋼集流體上電池電壓極化最小,併且具有較好的循環穩定性;鎳、銅次之;鈦集流體上的極化最大,循環穩定性也最差。併通過對比放電-充電循環前後電極和集流體錶麵的微觀結構,探討瞭集流體對電池性能顯著影響的原因。電解液對集流體會造成腐蝕,不同集流體在電解液中的穩定性有差異;正極材料塗覆在不同集流體上,電極錶麵狀況有差異;負載活性材料後集流體髮生腐蝕的電位有所降低,使集流體更易受到電解液的腐蝕。
이목전상용적Chevrel상Mo6S8작위정겁재료,도복재불동집류체(불수강、얼、동、태)상,이미위부겁,연구료재(PhMgCl)2-AlCl3/사경부남(간칭THF)“이대”전해액중집류체대가충미전지전화학성능적영향。항류방전-충전결과현시재불수강집류체상전지전압겁화최소,병차구유교호적순배은정성;얼、동차지;태집류체상적겁화최대,순배은정성야최차。병통과대비방전-충전순배전후전겁화집류체표면적미관결구,탐토료집류체대전지성능현저영향적원인。전해액대집류체회조성부식,불동집류체재전해액중적은정성유차이;정겁재료도복재불동집류체상,전겁표면상황유차이;부재활성재료후집류체발생부식적전위유소강저,사집류체경역수도전해액적부식。
The effects of different cathode current collectors (stainless steel, nickel, copper, and titanium) on the electrochemical performance of rechargeable magnesium batteries were investigated. Chevrel phase Mo6S8 acted as the cathode, (PhMgCl)2- AlCl3/tetrahydrofuran (THF) (the second generation electrolyte) as the electrolyte, and magnesium as the anode. Constant current discharge-charge results indicated that the electrochemical polarization of the electrode on stainless steel was the smal est and its cycling stability was the best, fol owed by nickel, copper, and titanium. Microstructure analyses for the electrodes and current col ectors before and after discharge-charge were analyzed to investigate the differing electrochemical performance. The electrolyte corroded the current col ectors to differing degrees. The surfaces of the electrodes differed after coating the active material on different current collectors. The corrosion potentials of the current collectors decreased after loading the active material. This resulted in the current collectors being more susceptible to corrosion by the electrolyte.