4.7 Article

Facile fabrication of WS2 nanocrystals confined in chlorella-derived N, P co-doped bio-carbon for sodium-ion batteries with ultra-long lifespan

期刊

DALTON TRANSACTIONS
卷 50, 期 41, 页码 14745-14752

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1dt01582f

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资金

  1. National Key Research and Development Program of China [2019YFC1904500]
  2. National Natural Science Foundation of China [NSFC 51502036, 21875037]
  3. Young Top Talent of Fujian Young Eagle Program
  4. Natural Science Foundation of Distinguished Young Scholars of Fujian Province [2019J06015]

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Utilizing waste chlorella as an adsorbent and bio-reactor, WS2 nanocrystals embedded in N and P co-doped biochar were successfully synthesized via a facile bio-sorption followed by sulphurization method. The WS2 nanocrystals contributed to storing more sodium ions and expediting their transportation, leading to improved capacity and reaction kinetics, demonstrating high specific capacity and superior rate performance for sodium-ion batteries.
Sodium-ion batteries (SIBs) have been regarded as a promising substitute for lithium-ion batteries but there are still formidable challenges in developing an anode material with adequate lifespan and outstanding rate performance. Transition metal dichalcogenides (TMDs) are promising anode materials for SIBs due to their high theoretical capacities. However, their severe volume expansions and low electronic conductivity impede their practical developments. In addition, the synthesis of energy storage materials from waste biomass has aroused extensive attention. Herein, we synthesize WS2 nanocrystals embedded in N and P co-doped biochar via a facile bio-sorption followed by sulphurization, employing waste chlorella as the adsorbent and bio-reactor. The WS2 nanocrystals are beneficial for storing more sodium ions and expediting the transportation of sodium ions, thus improving the capacity and reaction kinetics. Chlorella acts as a reactor and not only inhibits the stacking of WS2 nanocrystals during the synthesis process but also alleviates the mechanical pressure of composite during the charge/discharge process. As a result, the WS2/NPC-2 electrode delivers a high specific capacity (436 mA h g(-1) at 0.1 A g(-1)) and superior rate performance of 311 mA h g(-1) at 3 A g(-1) for SIBs. It also exhibits excellent stability even up to 6000 cycles at 5 A g(-1), which is one of the optimal long-cycle properties reported for WS2-based materials to date.

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