过电位
材料科学
多金属氧酸盐
纳米线
催化作用
阴极
铋
硫化物
密度泛函理论
纳米技术
电池(电)
氧化物
吸附
化学工程
储能
光电子学
无机化学
吸收(声学)
分解水
过渡金属
金属
硫化镉
作者
Guobao Yuan,Peishan Qin,Ziang Shang,Wenxing Chen,Zhiyi Sun,Junli Liu,Zhang Ye,Xun Wang
出处
期刊:Small
[Wiley]
日期:2026-01-15
标识
DOI:10.1002/smll.202514807
摘要
ABSTRACT The 1D sub‐1 nm nanowires (SNWs) usually possess a highly promising avenue in catalysis and energy storage fields owing to their high aspect ratios facilitating charge transport, and near 100% surface atomic exposure offering abundant active sites. However, current research is mainly focused on metal oxide SNWs, whereas the synthesis of sulfide SNWs has been rarely reported. Herein, a new kind of Bi 2 S 3 ‐phosphomolybdic acid (Bi 2 S 3 ‐PMA) SNWs induced by polyoxometalate clusters has been successfully prepared. Molecular dynamics simulation demonstrates that PMA and Bi 2 S 3 co‐assemble into stable 1D SNWs via non‐covalent interactions. Benefiting from the unique sub‐1 nm structure and the synergetic effects of Bi 2 S 3 and PMA, the SNWs exhibit enhanced light absorption ability, well‐matched energy band structure, and efficient separation/transfer capability of photo‐generated carriers. As the cathode catalyst in light‐assisted Li‐CO 2 batteries (LCBs), the Bi 2 S 3 ‐PMA‐based LCBs deliver a low overpotential of 0.22 V, superior cycling stability for 300 h at 0.01 mA cm −2 and 150 h at 0.05 mA cm −2 . Meanwhile, the battery also realizes an exceptionally long‐term lifetime of 4000 h under no light. Density functional theory calculations disclose that the presence of electron‐rich PMA promotes the adsorption of LiCO 2 and Li 2 CO 3 on SNWs, which further boosts battery efficiency.
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