Constructing　hybrid　heterostructures　of　transition-metal　dichalcogenides　is　an　effective　strategy　to　enhance　their　electrochemical　performance　and　stability　as　anode　materials　in　lithium-ion　batteries.　In　this　work,　a　facile　in　situ　strategy　was　developed　to　engineer　lattice-mismatched　MoS2-ZnS　together　with　C　into　hierarchical　nanostructures.　The　three-dimensional　architecture　was　constructed　using　few-layer　MoS2　nanosheets　as　the　building　block,　and　ZnS　and　C　coexisted　among　the　MoS2　nanosheets　with　a　mesoporous　structure.　By　the　synergy　effect　of　integrated　interfaces　and　hierarchical　configuration,　as-formed　heterostructures　exhibit　increased　conductivity,　enhanced　Car　transfer　efficiency,　and　retarded　volume　expansion　during　the　electrochemical　process.　All　of　these　contribute　to　the　greatly　increased　lithium　storage　capability　and　well-preserved　stability.　Impressively,　as-obtained　materials　exhibit　a　high　lithium　storage　capacity　of　961.9　mA　g(-1)　at　100　mA　g(-1)　after　100　cycles　(about　3.1　times　higher　than　pristine　MoS2　after　35　cycles),　good　rate　retention,　and　superior　cycling　stability　with　9.5%　decay.　Therefore,　the　proposed　strategy　provides　a　favorable　direction　for　developing　high-activity　and　low-cost　electrode　materials　with　potential　applications　in　electrochemical　fields.