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Heterostructures endow electrochemical hybrids with promising energy storage properties owing to synergistic effects and interfacial interaction. However, developing a facile but effective approach to maximize interface effects is crucial but challenging. Herein, a bimetallic selenide heterostructure is realized in a confined carbon network via an in situ electrochemical strategy to induce highly active and stable electrode architecture. The dynamically formed heterostructures upon repeated delithiation/lithiation process not only yield abundant interconnected SnSe2/FeSe2 heterojunctions with continuous channels for ion/electron transfer but maintain excellent conversion reversibility. Serving as anode for lithium storage, the SnSe2/FeSe2@C framework enables a high discharging capacity of 1781.9 mAh g−1 at 0.5 A g−1 after 500 cycles and superior cycling stability (no capacity fade after 1200 cycles at 2 A g−1). This study can guide future design protocols for interface engineering through the formation of dynamic channels of conversion reaction kinetics for potential applications in high‐performance electrodes. [ABSTRACT FROM AUTHOR]