福建师范大学环境与资源学院,福建 福州 350117
唐晨欣(2002—),女,硕士研究生,在读,研究方向为水系锌离子电池正极材料,E-mail:2426146458@qq.com;
卢至行,副教授,研究方向为二维纳米材料的可控制备与光电、催化、储能性质,E-mail:zxlu@fjnu.edu.cn。
收稿:2026-10-09,
修回:2026-10-23,
网络首发:2026-10-31,
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唐晨欣, 卢至行. K+预插层调控1T'-MoTe2层间结构及其水系锌离子电池储锌性能研究[J]. 储能科学与技术, XXXX, XX(XX): 1-12. DOI: 10.19799/j.cnki.2095-4239.2026.0862.
TANG Chenxin, LU Zhixing. K+ Pre-Intercalation Regulated Interlayer Spacing of 1T′-MoTe2 for High-Performance Aqueous Zinc-Ion Batteries[J]. Energy Storage Science and Technology, XXXX, XX(XX): 1-12. DOI: 10.19799/j.cnki.2095-4239.2026.0862.
唐晨欣, 卢至行. K+预插层调控1T'-MoTe2层间结构及其水系锌离子电池储锌性能研究[J]. 储能科学与技术, XXXX, XX(XX): 1-12. DOI: 10.19799/j.cnki.2095-4239.2026.0862. DOI:
TANG Chenxin, LU Zhixing. K+ Pre-Intercalation Regulated Interlayer Spacing of 1T′-MoTe2 for High-Performance Aqueous Zinc-Ion Batteries[J]. Energy Storage Science and Technology, XXXX, XX(XX): 1-12. DOI: 10.19799/j.cnki.2095-4239.2026.0862. DOI:
金属性1T′-MoTe
2
导电性优异,但其层状结构在Zn
2+
反复嵌入/脱出过程中易发生不可逆坍塌,导致容量快速衰减,限制了其在水系锌离子电池中的应用。针对这一问题,本研究提出K
+
电化学预插层策略,以CH
3
COOK溶液为电解液通过恒流充放电和循环伏安两步活化,将K
+
嵌入1T′-MoTe
2
/CC层间,以扩大层间距并缓冲体积变化,并系统探究了不同CH
3
COOK浓度对插层效果的影响。结果表明,1.0 M CH
3
COOK预插层效果最优,在0.2 A g
-1
下比容量由未插层的113 mAh g
-1
提升至260 mAh g
-1
,循环初期的容量骤降得到有效抑制。在1 A g
-1
下循环1200次,K-1T′-MoTe
2
/CC-1.0的容量保持率达到82.8%,远高于未插层样品的59.2%,库仑效率维持在约100%。不同扫速CV分析表明,插层后b值由0.715增至0.737,说明K
+
插层扩大了层间距,加快了离子迁移和扩散速率,改善了电极反应动力学。非原位XRD和SEM及循环后的XPS证实,K
+
预插层有效维持了活性材料循环过程中的层状结构和电极完整性。此外,该策略在2H-MoTe
2
和Chevrel相Mo
6
Te
8
中同样有效,初步验证了其在Mo-Te体系中的普适性。本工作为Mo-Te基材料在水系锌离子电池中的应用提供了可行的结构调控策略。
Metallic 1T′-MoTe
2
exhibits excellent electrical conductivity
but its layered structure is prone to irreversible collapse during repeated Zn
2+
insertion/extraction
leading to rapid capacity decay and limiting its application in aqueous zinc-ion batteries. To address this issue
this study proposes a K
+
electrochemical pre-intercalation strategy. Using CH
3
COOK solution as the electrolyte
K
+
is intercalated into the interlayers of 1T′-MoTe
2
/CC through a two-step activation of galvanostatic charge–discharge and cyclic voltammetry
thereby expanding the interlayer spacing and buffering volume changes. The effects of different CH
3
COOK concentrations on the intercalation are systematically investigated. The results show that 1.0 M CH
3
COOK pre-intercalation achieves the best performance. The specific capacity increases from 113 to 260 mAh g
-1
at 0.2 A g
-1
and the initial capacity decay is effectively suppressed. After 1200 cycles at 1 A g
-1
K-1T′-MoTe
2
/CC-1.0 delivers a
capacity retention of 82.8%
much higher than the 59.2% of the pristine sample
with the Coulombic efficiency remaining at approximately 100%. CV analysis at different scan rates shows that the b value increases from 0.715 to 0.737 after intercalation
indicating that K
+
intercalation expands the interlayer spacing
accelerates ion migration and diffusion
and improves electrode reaction kinetics. Ex situ XRD and SEM confirm that K
+
pre-intercalation effectively maintains the layered structure and electrode integrity of the active material during cycling. Moreover
this strategy is also effective in 2H-MoTe
2
and Chevrel-phase Mo
6
Te
8
preliminarily verifying its universality in the Mo-Te system. This work provides a feasible structural regulation strategy for the application of Mo-Te-based materials in aqueous zinc-ion batteries.
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