The　development　of　silicon-based　anode　materials　is　important　for　improving　the　energy　density　of　current　lithium　ion　batteries.　However,　there　are　still　strong　demands　for　these　materials　with　better　cycle　stability　and　higher　reversible　capacity.　Here,　a　kind　of　dual　bond　restricted　MXene-Si-CNT　composite　anode　materials　with　enhanced　electrochemical　performance　is　reported.　These　dual　bonds　have　been　clearly　revealed　by　an　X-ray　photoelectron　spectroscopy　technique　and　also　proven　by　theoretical　calculations　with　spontaneous　reaction　energy　values　(-0.190　and　-0.429　eV/atom　for　Ti-Si　and　C-Si　bonds,　respectively).　The　cycle　stability　of　the　composites,　prepared　by　a　facile　ball-milling　synthetic　method,　can　obviously　be　improved　because　of　the　existence　of　these　dual　bonds　and　the　multidimensional　constructed　architecture.　The　MXene-Si-CNT　composite　with　60　wt　%　silicon　possesses　the　best　overall　performance,　with　similar　to　80%　capacity　retention　after　200　cycles,　and　achieves　841　mAh　g(-1)　at　2　A　g(-1).　This　approach　demonstrates　a　promising　strategy　to　exploit　high-performance　anode　materials　and　lessens　the　immanent　negative　effect　of　silicon-based　materials.　Furthermore,　it　is　significant　to　extend　this　method　to　other　anode　materials　with　serious　volumetric　change　problems　during　the　cycling　process.