The Energy of a Continuous Charge Distribution (Griffiths EM Sect. 2.4.3 3rd ed)

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SUMMARY

The discussion focuses on the energy calculation of a continuous charge distribution as presented in Griffiths' "Introduction to Electrodynamics" (3rd ed., Section 2.4.3). The key formula derived for the work done is $$W = \frac{1}{2}\int\rho V d\tau$$, where $$\rho$$ represents the volume charge density and $$V$$ is the electric potential. The factor of $$\frac{1}{2}$$ is essential to correct for double counting in the energy calculations, which arises from the integral being the limit of a sum of point charges. The discussion clarifies that this factor remains consistent through the transition from discrete to continuous charge distributions.

PREREQUISITES
  • Understanding of electric potential and charge distributions
  • Familiarity with integral calculus and limits
  • Knowledge of Griffiths' "Introduction to Electrodynamics" concepts
  • Basic principles of electrostatics and energy calculations
NEXT STEPS
  • Study the derivation of energy in continuous charge distributions in Griffiths EM, focusing on Section 2.4.3
  • Explore the Bliss Theorem and its implications for integration in electrostatics
  • Learn about the differences between point charge and continuous charge distribution calculations
  • Investigate applications of line and surface charge densities in electrostatics
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Students of electromagnetism, physicists, and educators seeking a deeper understanding of energy calculations in continuous charge distributions as outlined in Griffiths' textbook.

zackiechan
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Homework Statement
just confused about the derivation/justification
Relevant Equations
for point charge distribution ##\frac{1}{2}\sum_{i=1}^{n}*q_i*V(\vec{r_i})##

for a continuous (volume, but the same ##\frac{1}{2}## applies to the line and surface formulas): ##\frac{1}{2}*\int\rho V d\tau##
I'm working through Griffiths EM 3rd ed. in section 2.4.2 (point charge distribution) and 2.4.3 (continuous charge distribution).

I understand from the section on point charge distributions that when we add up all the work (excluding the work necessary in creating the charge itself), one clever way to do it is to sum and double-count every pairwise interaction (of course excluding self-interaction):
$$W = \frac{1}{2}\sum_{i=1}^{n}q_i\left(\sum_{j=1\\ j \neq i}^{n}\frac{1}{4\pi\epsilon_o}\frac{q_j}{\mathcal{r_{ij}}}\right) \hspace{10 mm} \mathcal{eqn. 1}$$
then correct for the double-counting by that factor of ##\frac{1}{2}## in front of the sum.

He goes on to recognize the term in parentheses as the potential at ##V(\vec{r_i})## and cleans it up as $$W = \frac{1}{2}\sum_{i=1}^{n}q_iV(\vec{r_i}). \hspace{10 mm} \mathcal{eqn. 2}$$

In the next section he just writes down the continuous volume charge density analog as: $$W = \frac{1}{2}\int\rho V d\tau \hspace{10 mm} \mathcal{eqn. 3}$$

He quickly mentions the line and surface analogs as ##\frac{1}{2}\int\lambda V dl \hspace{5 mm} \frac{1}{2}\int\sigma V da##.

I'm confused as to why the ##\frac{1}{2}## is still in the integral for the continuous charge distribution cases?
When do we double count to have to correct by that factor of 2?
Is the ##\frac{1}{2}## a consequence of having recognized a piece of the double sum as a potential ##V(\vec{\mathcal{r_i}})##?
Does using the potential automatically double-count?
 
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An integral (of a continuous distribution) is the limit of a sum of point charges (more and more, but smaller and smaller charges), so the factor of ##1/2## will remain through the limiting process.
 
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To add above,we know that integration is limiting process. Here we just consider an infinitesimal charge ##dq##. Now, all the mathematical steps are same as you did for point charge ##q##. We will replace this with an infinitesimal charge ##dq##. As ##dq \rightarrow 0 ## , we replace our sum with integration( This is due to Bliss Theorem)
 

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