--%>

What is schrodinger wave equation?

The Schrodinger wave equation generalizes the fitting-in-of-waves procedure.

The waves that "fit" into the region to which the particle is contained can be recognized "by inspection" only for a few simple systems. For other problem a mathematical procedure must be used. The Schrodinger wave equation, suggested by Erwin Schrodinger in 1926, provides one method for doing this. You will see, when we again do the particle-on-a-line problem, that this equation extends the pictorial fitting-in-of-waves procedure.

Think of the method in which the Schrodinger equation is used as the counterpart of the more familiar classical parts in which Newton's laws are used. Recall that equations, such as ƒ = ma, based on Newton's law are presented without derivation. These laws let us calculate the dynamic behavior of ordinary objects. We accept Newton's laws and the equation derived from because the results are agree from experiment. Schrodinger's equation is also presented without derivation. We accept the results that we obtain by using it because in all cases where the results have been tested, they have been in agreement with experiment. Just as one uses and trusts ƒ = ma, so one must use and, to the extent that seems justified, trust the Schrodinger equation.

The Schrodinger equation, as with the direct use of the de Broglie waves, leads to waves from which all other information follows. From these waves, we obtain immediately the allowed energies of any confined particle and the probability of the particle being at various positions.

We begin by writing the form of the Schrodinger equation that lets us deduce the waves, and then the energies and position probabilities, for a particle that moves along one dimension. Let x be the variable that locates positions along this dimension. The behavior of the particle depends on the potential energy that it would have at various positions. Let U (x) be the mathematical function that describes the potential energy. The Schrodinger equation requires us to supply this function and to indicate the mass m of the particle being treated.

Solutions of the Schrodinger equation are in the form of mathematical functions that shows the amplitude of the wave at various x places. The square of this function gives the relative probability of the particles being at various positions. The energies for which these probabilities of the particles exist are the energies "allowed" to the particle.

The Schrodinger equation can be viewed as a method in which wave properties yield the total energy of a particle as the sum of its potential and kinetic energies. The potential energy contribution is given by the Schrodinger equation as a "weighting" of the potential energy at each position according to the value of the wave function at that position. The kinetic energy contribution of the first term can be appreciated by reference to the particle on a line results. The particle-on-a-line example produced the quite general result that waves for the highest energy of the wave function, the greater the kinetic energy, the greater the curvature of the wave function.

The general energy relation:

KE + PE = total energy

Becomes the one-dimensional Schrodinger equation;

-h2/8∏2m Χ d2?/dx2 + U(x)v = ε?

The potential energy contribution is given by the Schrodinger equation as a "weighting" of the potential energy at each position according to the value of the wave function amplitude at that position.

The kinetic-energy contribution fo the first term can be appreciated by reference to the particle-on-a-line results. The particle-on-a-line example produced the quite general result that the waves for the higher energy states had more nodes than the waves for the greater the curvature of the wave function, the greater the kinetic energy. This shows up in the Schrodinger equation as a relation between the second derivate of the wave function and the kinetic energy.

The behavior of a particle is deduced by finding a function and the kinetic energy will solve the differential equation after an appropriate expression for U (x) has been substituted. Solution functions generally exist for certain values for the allowed energies of the particle. The probability function also obtained from the solution function. In general may be either a real or a complex function. To allow for the second possibility, we should write not a sign but where implies the product of the wave function and its complex conjugate. Here we do not deal with problems that lead to complex wave functions. The probability is given by the simple squared term. 

   Related Questions in Chemistry

  • Q : Inorganic Chemistry Inorganic

    Inorganic Chemistry:In the year 1869, Russian Chemist Dmitry Mendeleyev forms the periodic table of the element. Since Newlands did before him in the year 1863, Mendeleyev categorizes the el

  • Q : Formula of diesel Write a short note on

    Write a short note on the formula of diesel, petrol and also CNG?

  • Q : Problem on partial pressure i) Show

    i) Show that the equilibrium constant Kp for the reaction CaCo3(s) ↔ CaO(s) +CO2(g)is about unity (i.e. = 1.0) at 895 °C.ii) If two grams of calcium carbonate are pl

  • Q : Explain Solid Compound Formation. In

    In some two component, solid liquid systems, a solid compound forms.In systems in which the components have an interaction for such other, a solid state compound of the two compounds of the two components can form.Formic acid and formaide form a solid state, one-to-one com

  • Q : Solution density of water is 1g/mL.The

    density of water is 1g/mL.The concentration of water in mol/litre is

  • Q : Number of mlecules in methane Can

    Can someone please help me in getting through this problem. The total number of molecules in 16 gm of methane will be: (i) 3.1 x 1023 (ii) 6.02 x 1023 (iii) 16/6.02 x 1023 (iv) 16/3.0 x 1023

  • Q : Electrochemistry ( electrolysis of

    1. Define Faraday's first law of electrolysis 2. define Faraday's second law of electrolysis

  • Q : Question based on relative lowering of

    Give me answer of this question. When a non-volatile solute is dissolved in a solvent, the relative lowering of vapour pressure is equal to: (a) Mole fraction of solute (b) Mole fraction of solvent (c) Concentration of the solute in grams per litre (d) Concentratio

  • Q : Dipole moment of chloro-octane Describe

    Describe the dipole moment of chloro-octane in brief?

  • Q : Colligative properties give atleast two

    give atleast two application of following colligative properties