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All‐pH Stable Sandwich‐Structured MoO 2 /MoS 2 /C Hollow Nanoreactors for Enhanced Electrochemical Hydrogen Evolution
Author(s) -
Gong Feilong,
Liu Mengmeng,
Ye Sheng,
Gong Lihua,
Zeng Guang,
Xu Lin,
Zhang Xiaoli,
Zhang Yonghui,
Zhou Liming,
Fang Shaoming,
Liu Jian
Publication year - 2021
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.202101715
Subject(s) - nanoreactor , tafel equation , materials science , electrochemistry , chemical engineering , molybdenum , metal , catalysis , oxide , hydrogen , reversible hydrogen electrode , inorganic chemistry , nanotechnology , electrode , chemistry , organic chemistry , reference electrode , nanoparticle , engineering , metallurgy
Molybdenum sulfide has great potential for the electrocatalytic hydrogen evolution, but its structural instability in acidic media and high barriers in alkaline/neutral media limits its practical applications. Herein, the design of monodispersed sandwich‐structured MoO 2 /MoS 2 /C hollow nanoreactors is reported with a triple layer “conductor/catalyst/protector” configuration for efficient electrochemical hydrogen evolution over all pH values. Metallic MoO 2 substrates with ultrahigh pristine electroconductivity can promote the charge transfer while sulfur vacancies are introduced to activate the highly exposed (002) facets of MoS 2 . The optimized MoO 2 /MoS 2 /C nanoreactor exhibits overpotentials of 77, 91, and 97 mV (10 mA cm −2 ) and Tafel slopes of 41, 49, and 53 mV dec −1 in acidic, alkaline, and neutral media, respectively, which are much better than most of the MoS 2 ‐based electrocatalysts. Moreover, defective carbon shells are in situ generated, preventing the electrocatalysts from corrosion in acidic and alkaline media; the structural stability is verified via in situ Raman and XRD characterizations. Based on the density functional theory calculations, vacancy engineering can regulate the band structures, electron density differences, total density of states, and the H* and H 2 O adsorption‐dissociation ability over the entire pH range. The findings may shed light on the rational development of practical pH‐universal electrocatalysts for durable hydrogen evolution.