Regulating local chemical softness of the collector to homogenize Li deposition for anode-free Li-metal batteries

被引:1
|
作者
Zhu, Jiaming [1 ]
Kang, Cong [1 ]
Xiao, Xiangjun [1 ]
Mao, Ya [2 ]
Luo, Ying [2 ]
Wang, Yuheng [3 ]
Zhang, Quansheng [3 ]
Ma, Yulin [1 ]
Du, Chunyu [1 ]
Lou, Shuaifeng [1 ]
Kong, Fanpeng [1 ,4 ]
Xie, Jingying [2 ]
Yin, Geping [1 ]
机构
[1] Harbin Inst Technol, Sch Chem & Chem Engn, State Key Lab Space Power Sources, Harbin 150001, Peoples R China
[2] Shanghai Inst Space Power Sources, Shanghai 200245, Peoples R China
[3] Shanghai Inst Technol, Sch Chem & Environm Engn, Shanghai 201418, Peoples R China
[4] Chongqing Res Inst HIT, Chongqing 401135, Peoples R China
基金
中国国家自然科学基金;
关键词
LITHIUM; GRAPHENE;
D O I
10.1039/d4ee03673e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Regulating the surface structure of the collector to synergistically reduce the nucleation and lateral growth barrier of Li+ electrodeposition is key to long-cycle anode-free Li-metal batteries (AFLMB), but its adjusting mechanism and modulation remain a formidable challenge. Herein, a previously unreported heterogeneous collector with hard-base sites and soft-acid sites is proposed to enhance chemical interaction with hard-acid Li+ and soft-base Li atoms, respectively. Theoretical analysis demonstrates that the addition of Co single atoms into the N-C host improves the hardness of N bases and the softness of the carbon matrix. According to the results of operando microscopy and electrochemical measurement, the HBSA-Co SA collector with controlled local chemical softness substantially reduces nucleation/growth barriers without any dendrite morphology. The NCM811-based Li metal cells with a high cathode area capacity of 15 mA h cm-2 and limited lithium excess achieve a superior capacity retention rate of 98.8% after 150 cycles. This finding provides an avenue to rationally design a highly efficient collector for AFLMB.
引用
收藏
页码:9323 / 9334
页数:12
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