Dual Nature
Dual Nature
Dual Nature
given by HERTZ
·
E h0
=
E hc
=
=
x wavelength
=
↳
I n 6.626x10
=
-
34
⑦ ⑦ O
5/5 ⑦
⑦ ⑦
E 0er 100 ev O ⑦ ⑦ ⑦ ⑦ ⑦
⑦
=
=
x(nm) x (A) ⑦ ⑦ ⑦
⑦ ⑦
MARY
*
PARTICLE
NATURE
OF LIGHT
↑
Phatans= The radiation hit the metal do not
energy
· which
surface in photo-electric
effect
packets quanta
-
of came in the
farm of waves instead
they show particle nature
of light quanta of
I
energy
E no frequation
=
-
hC
-
7-
- -> instead
of being a
does not always behaves like It has parside nature also. The
Light a wave.
·
define particle nature of lightwithouttaking wave nature into accordance and vice-versa
SUMMARY
-
PROPERTIES OF PHOTON
reference
frame of refer. phaton neutral and remains undeviated under electric and
A ·
is
The
frame through magnetic field
and momentum
which speed and ·
each phatan has
definite energy
vel of a
body is
defined E hC=
PA
=
I N
Panatan hC/x F ·
Phatans
of light of a particular wavelength have same
energy
and
momentum
P h/x The collision
of phatan particle isassumed to be perfectly elasti
material
=
·
a with a
overall
·
dash collision
(refer back) REMARKS
-
-
⑦
EMISSION OF
2 FROM METAL SURFACE
present
on metal may as compared to 20in the bulk of the metal
that
are
loosely bound. Such cos are called electrans
free
Thermionic emission electron
Thermians free
28
Photoelectric emission
Thermionic emission- electrons emitted thermally healing metal (THERMIONS)
by
Field emission -> metal placed between a
high electric
field
Photoelectric emission- The emission
of electrone when a
high energy
radiation made to metal
is
fall on a
SUMMARY
WORK FUNCTION
surface eO ·
The minimum amount
of energy required to remove a
surface et
iscalled
work
function of the metal
resume lowest I -
If the supplied energy is
greater than work
function even then there is no
guarantee of et emission as co
may
laase energy while
colliding with cans
KEmai supplied -
energy I Ec 6 and electron makes bestuse
of incident the electron
energy,
->
come with
out KoE
may
a
called work
function. Dothe supplied energy of then electron
may came with
out a
Kinetic
energy
SUMMARY
-
-
THRESHOLD FREQUENCY
frequency of incident light
that
makes up the work
· The min
for function for the emission
-= (threshold
I of electron
greaency)
eo emission)
Umin I = == /Yar 6 hfo
=
h no
threshold
6 hvo
(r= frequency) KE
= ↑
(another eg far () mas
el
Lemitted
KEmax E = -
k
KE hU-hVo
max
=
oneo
y
mx +
C 5 (frequency)
Tvo
=
of phaton
=
no incident
d
=
The be than
frequency must
higher threshold
frequency for emission.
·
SUMMARY
-
-
TRESHOLD WAVELENGTH
et be emitted
may is
·
x = ha
I I = 0
=0 mas
(Threshold hC
"mas=
mission
ha R
I d
=
I wavelength) ⑰
< Do
far
emission ·
The max
wavelength for which so
may seemilled threshold
is wavelenght
KE
KEmax
4-
=
-
KEma hc=
(I) -E?
y.
mx c
y
+
=
q 5.
=
must
SUMMARY
-
-
CHOTO CURRENT
cathode wartz window
positive paten an
anode
anade. ⑧ > as eO
-- as
-
re
↓
saturation current phatasensitive plate + Ve
current
when photo
wavelength
chart made to
fall metal plate (cathode)
lightof
an an
current become . is
no
is
potential on anade no
free electrons are able to
not came out became of
repulsion. patential is anode et
start to
e-e When the applied on
flow.
certain limit, and does not
constant
After a the
photocurrent
becomes increase
·
The
even on
increasing the
potential. current
iscalled saturation current
·
When manchromatic
light ismade to fall an calhade to start
flowing towards anade
Phatourrent
with the potential. The current formed opp. to flow of t called
is
SUMMARY
-
STOPPING POTENTIAL
stopping potential if in the above case, I anade is given-ve potential wet
cathode, et;
stopping voltage (vo) are repelled and photocurrentdecreases
·
Iwe keep
decreasing anode patential (making more and
it
more-vel, a
stage
Vo (KE) mas
=
comes when no et
can reach (A) and photocurrentbecomes zero. Thistrade
C
patential which stops
any et
from reaching anade is called
stopping
patential an is
topping valtage (vo) used in
work
electrastatic
curril against farce
Elphato aturation KEmax O
KElmax q DV =
⑧
(KE) max eVo
=
Vo
patent)
-
canode
Vo
KElmas
=
E= radiation
incident
energy
y> fo
for
emission
masterre e
↓
alope=h/e
y
manda I
mx
=
c
+
.
& Greq.
STOPPING POTENT US WAVELENGTH INCIDENTPROTON
OF
·
kF E =
-
0
x< o Vo
KE
4-
=
for emission
-
** - =
,
slope -
Vo
e e
=
-
y mx +
=
c
"xo
* e.=
INTENSITY AND PHOTOCURRENT
① intensity increase - no.
of Phatans increase
Photocurrent
Patent
Intensity
intensity
elec. Then
· Gives relation between
intensity and photocurrent. If phatan gives rise to a
increase in a no.
of phatans results increase
in in no,
of photoelectrons which leads to increase
in photocurrent.
INTENSITY AND STOPPING POTENTIAL
Phatourrent ·vo
()max El
=
stopping patential vo
e
b
and
intensity stopping
=
phatocument
1
=
phatocurrent
1
12 1 =
Has
frequency depends an
stopping patent
3
2 I
>Vo
·
Shaws there
that is no relation between intensity and stopping potential
intensity depends on
phatacument. frequency depends an
stopping patential
PARTICLE NATURE
centurewave
·Thewavematureaswelldefinedbya the
nature
of light
RI) in wave
of lightan increasing intensity the amplitude of wave
nature increases
(IXA2) increasing KE. But this data is experimentally wrong as Intensity
does not
depend an IE
R2) existence
of threshold frequency
If lightis lightof low incident
a wave, then even is
a
frequency is
·
metal
on surface, then electran keeps on
absorbing energy and should
R3) ejection
instant
of photoelectran. (No time delay)
·
over a
large no.
of electrons so would
energy per et be des and hence
There will
be lime
delay for et
eminion does not
(This happen)
according to
DeGraglic- every moving particle has a wave associated
to t
-> This iscalled matter wave
wavelengthe naturel
The
wavelength of matter wave (N=
b momentum (particle naturel
X1 = De Braglie
mV
wavelength
for subatomic
significant
->
particles X is
X in TERMS KE
OF
x
tx =
.
=
(k)
x =
0 mv v1 kF
bmv2
=
= =
e
KE m
I
x
=
=
X=
=
h
2m(kE) KE
1
= 2 am(E)
P
=
=
2m(kE)
X in TERMS OF
ACCELERATING POTENTIAL
KE eVo
=
gAV
=
x 1
=
for any x h
particle x 1
=
2mqar ->
=
am(KE) 2mq5V
x 1
50 =
=
2 mer
5Imer- I =
12027
=
-
to
just putKE eVo=GAV =
in the equ
x=IKE getrelation of
lambda with
stopping potential
SUMMARY
DE-BROGLIE (X) FOR GAS MOLECULE
manatomic
far gas
·
kT
X h =
kE =
3mkT
(I molecule) x
b amk.E
= n
=
I
my mass maleale 2m.
KT
K= baltzmann canst
K= baltzmann constant x 1
=
6.022x102 males x
= 25
n X = h -
=
I molecule AM 3
a KT
=
M- malecular may NA
T- temp in Kelvin
M5 kg x metre
=
DAVISSON AND GERMER SETUP
callimater (so that
et
go straight
It through it
--
Tungsten
e8
------------
,
Barium eO
oxide
,
caling (law 0)
/
eG
law voltage Nickel
, crystal
sliding
galvanom. circular
collector
WORKING
ct are emitted
from Barium oxide
coating of electrically heated
tungsten
·
filament
·
These et
are accelerated
through a patential (v)
These accelerated electrons strike nickel and are scattered
crystal
·
in all directions
movable collector (an circular scale) collects et's at
a
differentangles
·
* The experiment
was
performed between
with
diff, accelerating patential but
significant
observered
intensity was un-68V
⑧
⑦( ⑧
⑧
↑
d=distance between
d crystal layer
⑧ ⑧ ⑳
↓ ·-
angle between incident
beam
and atomic
layer
X- beam
incident
⑳ . ⑧
wavelength of
for Nickel d 0.91
=
A = 0.91x10-10m n Maxima
1,2,3
=
----
0 50°
= 0+ 412 90 0658
=
92.91Avin6s =X (n = 1
firstmax
X 1.6SA
=
= 1.65
Check I