Bandingkan metode

	DFT Waktu-Bergantung	Teori Fungsional Kerapatan
Bidang	Komputasi Kuantum	Komputasi Kuantum
Keluarga	Machine learning	Machine learning
Tahun asal	1984	1965
Pencetus	Erich Runge and Eberhard Gross	Walter Kohn
Tipe	Excited state method	Electronic structure method
Sumber perintis	Runge, E., Gross, E. K. (1984). Density-functional theory for time-dependent systems. Physical Review Letters, 52, 997–1000.	Kohn, W., Sham, L. J. (1965). Self-consistent equations including exchange and correlation effects. Physical Review, 140, A1133–A1138.
Alias	TDDFT, TDDFT/DFT	DFT, Kohn-Sham equations
Terkait	3	4
Ringkasan	Time-Dependent Density Functional Theory (TDDFT) extends DFT to excited states and time-dependent phenomena. Formulated by Runge and Gross in 1984, TDDFT enables calculation of excitation energies, optical spectra, and charge-transfer processes with moderate computational cost, making it invaluable for photochemistry and materials science.	Density Functional Theory (DFT) is a computational method for determining the properties of materials and molecules by modeling the ground state electron density. Developed by Walter Kohn and Lu Jeu Sham in the 1960s, DFT reduces the complexity of quantum chemistry from tracking individual electron coordinates to optimizing the total electron density, enabling efficient simulations of large molecular and condensed-matter systems.